Multipotent mesenchymal stromal cells: A promising strategy to manage alcoholic liver disease

Abstract

Chronic alcohol consumption is a major cause of liver disease. The term alcoholic liver disease (ALD) refers to a spectrum of mild to severe disorders including steatosis, steatohepatitis, cirrhosis, and hepatocellular carcinoma. With limited therapeutic options, stem cell therapy offers significant potential for these patients. In this article, we review the pathophysiologic features of ALD and the therapeutic mechanisms of multipotent mesenchymal stromal cells, also referred to as mesenchymal stem cells (MSCs), based on their potential to differentiate into hepatocytes, their immunomodulatory properties, their potential to promote residual hepatocyte regeneration, and their capacity to inhibit hepatic stellate cells. The perfect match between ALD pathogenesis and MSC therapeutic mechanisms, together with encouraging, available preclinical data, allow us to support the notion that MSC transplantation is a promising therapeutic strategy to manage ALD onset and progression.

Key Words: Alcoholic liver disease; Cellular therapy; Alcoholic steatohepatitis; Hepatic function recovery; Mesenchymal stem cells

Core tip: Chronic alcohol consumption is a major cause of liver disease. Stem cells, in particular multipotent mesenchymal stromal cells (MSCs), have been envisioned as a promising tool for the development of therapeutic strategies to treat alcoholic liver diseases (ALD). The advantages of MSC include the regulation of exacerbated inflammatory process, their differentiation into hepatocytes, the production of trophic factors that prevent the apoptosis of parenchymal cells, and the induction of the proliferation of endogenous progenitors. Here, we revise the pathophysiology of ALD to identify therapeutic targets for MSCs. Also, we discuss the rationale to propose an MSC-based therapy to treat ALD.

ALCOHOLIC LIVER DISEASE

Chronic alcohol consumption is a major cause of liver disease[1-3]. Moreover, alcohol consumption negatively impacts the natural history of other types of chronic liver diseases such as nonalcoholic steatohepatitis, and hepatitis B and C, favoring fibrosis progression[3-5]. Alcoholic liver disease (ALD) comprises a broad spectrum of disorders, encompassing simple steatosis, steatohepatitis, and cirrhosis. The pathomechanism associated with ALD involves complex interactions between the deleterious effects of alcohol and its toxic metabolites on various cell types in the liver, the induction of reactive oxygen species (ROS), and the up-regulation of the proinflammatory cascade[1,3].

Alcoholic steatosis, the earliest manifestation of ALD, is present in more than 90% of heavy drinkers, and is pathologically characterized by microvesicular and macrovesicular fat accumulation within hepatocytes, minimal inflammatory reaction, and no hepatic fibrosis[1]. This stage is asymptomatic and reversible with alcohol abstinence[6]. Alcohol consumption increases the ratio of NADH/NAD⁺ in hepatocytes, which disrupts mitochondrial β-oxidation of fatty acids, leading to steatosis development[7]. Alcohol consumption also increases fatty acid triglycerides synthesis through the upregulation of the sterol regulatory element binding protein 1c[8] and the downregulation of the peroxisome proliferator-activated receptor-α[9]. ALD progression is characterized by steatosis, a superimposed inflammatory infiltrate of predominantly polymorphonuclear leukocytes and hepatocellular damage. When the inflammation and hepatocellular injury are severe, the condition is termed steatohepatitis and is associated with a high mortality rate[10,11].

The pathogenesis of alcoholic steatohepatitis is complex and multifactorial. In the liver, alcohol is metabolized primarily into acetaldehyde by the enzymes alcohol dehydrogenase in the cytosol, cytochrome P450 in microsomes, and catalase in peroxisomes[12]. Acetaldehyde is highly toxic to hepatocytes because it binds to proteins and DNA, forming adducts that promote glutathione depletion, lipid peroxidation, and mitochondrial damage[13,14]. Additionally, these adducts act as antigens that activate the adaptive immune response, leading to lymphocyte recruitment to the liver[15]. Acetate resulting from acetaldehyde breakdown is rapidly released from the liver into circulation and then metabolized into CO₂via the tricarboxylic acid cycle in skeletal muscle, brain, and heart. Although acetate has no direct hepatotoxicity, it is believed that it can regulate the inflammatory response in patients with alcoholic steatohepatitis through the upregulation of proinflammatory cytokines released by macrophages[16].

Alcohol abuse also results in changes in colonic microbiota and increased gut permeability, leading to translocation of bacterial products, such as lipopolysaccharide, into the portal circulation[17]. In Kupffer cells, lipopolysaccharide activates the MyD88-independent signaling pathway through toll-like receptor 4, resulting in the production of oxidative stress and proinflammatory cytokines such as tumor necrosis factor (TNF)-α, contributing to hepatocellular damage[18,19].

Histologic features of alcoholic steatohepatitis include inflammation and necrosis, which are more prominent in the centrilobular region of the hepatic acinus, while hepatocytes are classically ballooned, leading to compression of the sinusoid and portal hypertension[20,21]. Alcoholic cirrhosis is the end stage of ALD and is characterized by distortion of the hepatic architecture, septum formations, rings of scars that surround hepatocyte nodules, the formation of regenerative nodule, and the loss of liver function[22].

Extracellular matrix (ECM), particularly collagen type I, is mainly produced by activated hepatic stellate cells (HSCs), located in the space of Disse between the hepatocytes and sinusoids. HSCs can be activated by neutrophils, damaged hepatocytes, and activated Kupffer cells through various profibrogenic mediators, including transforming growth factor (TGF)-β, TNF-α, and ROS[3,23]. Additionally, ROS downregulate the action of metalloproteinases and upregulate tissue inhibitor of metalloproteinase-1, resulting in greater collagen accumulation[24].

Along with other liver diseases, patients with cirrhosis are at risk for hepatic decompensation (ascites, variceal bleeding, and encephalopathy) and the development of hepatocellular carcinoma[25,26]. Although the most important risk factor for ALD is the absolute amount of alcohol intake, only approximately 35% of heavy drinkers develop advanced ALD, indicating that other factors are involved in host susceptibility to the disease. These factors include sex, obesity, drinking pattern, dietary factors, non-sex-linked genetic factors, and cigarette smoking[27-30].

CURRENT ALD TREATMENT

Despite the profound economic and health impacts of ALD, little progress has been made in the management of patients with this condition, and medical treatment has not changed significantly in the last 45 years[10,31,32]. Although nutritional and supportive management are important, alcohol abstinence is the mainstay therapy for patients with all stages of ALD[33,34]. However, the benefits of alcohol abstinence may not be sufficient for patients with decompensated ALD, such as cirrhosis or severe alcoholic hepatitis[35,36].

Corticosteroids were one of the first pharmacologic therapies investigated for the treatment of alcoholic hepatitis. Despite the widespread awareness and use of this therapy, controversy still exists regarding its true efficacy[37]. Taking into account the participation of TNF-α in ALD pathogenesis, TNF-α antagonists have also been studied for this condition. Although the initial studies were promising, larger clinical trials demonstrated an increased risk of infection and mortality with these agents[38]. In addition, pharmacologic therapy with medications such as disulfiram, baclofen, colchicine, vitamin E, and naltrexone have been considered, although their efficacies are limited[3,39,40].

The most effective therapy for advanced cirrhosis is liver transplant, however, the scarcity of donors, surgical complications, immunologic suppression and rejection, and high medical cost limit its availability and clinical utility[41]. Moreover, liver transplantation is not an option for most patients, and, until now, no other treatment has demonstrated superiority over steroids. Therefore, alternative therapies are needed. To this end, alternative approaches that circumvent the use of the whole organ, such as transplantation of cells of diverse origins, have been proposed in recent years[42].

CELLULAR THERAPY FOR LIVER REGENERATION

It is well known that the liver has a high regenerative capacity. Under normal conditions, recovery of liver mass occurs mainly via proliferation of remaining adult hepatocytes. On the other hand, under pathologic conditions in which the proliferation of hepatocytes is inhibited, liver progenitor cells (oval cells) proliferate and differentiate into hepatocytes or biliary epithelial cells[43]. Chronic ethanol exposure and sustained inflammation have been shown to inhibit DNA synthesis in the damaged liver[44,45]. This impaired hepatocyte proliferation is the consequence of oxidative damage by the ROS produced from alcohol metabolism[46]. Moreover, ethanol could inhibit early differentiation of hepatic progenitor cells into functional mature hepatocytes[47].

Cell therapy for the treatment of hepatic fibrosis has been evaluated in different animal models, and some findings have been very encouraging. The transplantation of mature hepatocytes into human patients has provided insights into the way in which human liver disease could be treated by cellular therapies[48]. However, the high number of cells needed for the transplantation, the availability of fresh cells or the quality of cryopreserved ones, and the necessity of immunosuppression to avoid the rejection of transplanted cells are the main limitations of adult hepatocyte transplantation[49,50]. Immunosuppression is a particularly important point, as the hepatic failure itself increases the risk of developing septic complications, which are worsened by the use of immunosuppressive drugs.

Numerous studies have focused on investigating the ability of a variety of stem cells that can be readily isolated using noninvasive procedures to give rise to hepatocytes both in vitro and in vivo[51]. Considering that some of these stem cell populations are present in adults, it would be possible to produce personalized immunologically matched hepatocytes[52]. Moreover, adult stem cells have the ability to reduce the hepatic proinflammatory microenvironment, inhibit the activation or induce apoptosis of HSCs, and promote the regeneration of residual hepatocytes[53,54].

MESENCHYMAL STEM CELLS AS A TOOL FOR THE INDUCTION OF TISSUE REGENERATION

The aim of regenerative medicine is to develop therapeutic strategies for the management of severe injuries or chronic diseases in patients whose endogenous regenerative mechanisms have failed to restore the impaired functions. Over the past years, stem cells have been envisioned as the best tool for this purpose. Stem cell-based intervention is known to act through multiple mechanisms, which is a clear advantage when facing diseases with a complex pathophysiology, such as ALD.

In general terms, adult stem cells are found in all nonembryonic tissues, where they contribute to both maintenance of cellular homeostasis and regeneration of damaged organs. These cells are multipotent and can be isolated from a fetus, newborn, child, or adult, and due to their limited self-renewal potential, they are not teratogenic. Some of them also have plasticity, i.e., they can differentiate into cells from lineages different from their origin[55].

As adult stem cells pose fewer bioethical and technical concerns than embryonic stem cells, the first candidate for a stem cell-based strategy to treat liver regeneration was bone marrow-derived stem cells[53,56-58]. Bone marrow harbors at least two distinct adult stem cell populations: the hematopoietic stem cells that give rise to blood and endothelial cells[59] and the multipotent mesenchymal stromal cells, also referred to as mesenchymal stem cells (MSCs), that provide support to hematopoietic stem cells and drive the process of hematopoiesis[60]. In addition to bone marrow, MSCs have now been isolated from numerous tissues, including liver, lung, umbilical cord, skeletal muscle, dental pulp, spleen, and adipose tissue[61-63]. Thus, it has been postulated that MSCs play a critical role in organ homeostasis by providing supportive factors to the surrounding tissue.

One of the main technical difficulties associated with the therapeutic use of MSCs is the lack of a specific antigen for their identification. Therefore, in 2006, the International Society for Cellular Therapy proposed minimal criteria to define human MSCs (hMSCs): (1) must be plastic-adherent when maintained under standard culture conditions; (2) must express CD105, CD73, and CD90, and lack the expression of CD45, CD34, CD14, CD11b, CD19, and class II human leukocyte antigen surface molecules; and (3) must differentiate into osteoblast, adipocytes, and chondroblasts under in vitro differentiation conditions[64,65].

Despite the scarcity of MSCs (< 0.01% of the mononuclear cells present in the bone marrow), they can be considered as ideal candidates for cell therapy because: (1) they can be obtained from donors without major complications; (2) they can be easily expanded ex vivo; (3) when MSCs are systemically administered, they can selectively migrate to and engraft damaged tissue. The migration of MSCs is facilitated by the release of several molecules from the damaged tissues that interact with different receptors expressed by the MSCs[66,67]; (4) it has been suggested that MSCs cross the germ line barrier and generate cells from the endodermal and ectodermal lineages[55]; (5) MSCs secrete a broad range of bioactive growth factors, including vascular endothelial growth factor (VEGF), basic fibroblast growth factor, insulin-like growth factor (IGF), hepatocyte growth factor (HGF), and epidermal growth factor (EGF)[68]. Therefore, MSCs could provide trophic support to injured tissue by modifying the microenvironment to induce local precursor proliferation and differentiation, improving damaged tissue irrigation, and preventing parenchymal cell apoptosis[55,68]; and (6) MSCs are hypo-immunogenic[69], which represents the main advantage of MSCs over hematopoietic stem cells for clinical use, as histocompatibility between donor and receptor is not required and the recipients do not need to be conditioned before MSC transplantation[70]. Furthermore, MSCs have been administered to more than 1000 human patients with no evidence of adverse effects or tumor formation[70] (Table 1).

Table 1 Proposed cellular and molecular mechanisms that could contribute to hepatic protection by mesenchymal stem cells in alcoholic liver disease.

MSCs in liver inflammation

Inhibit the proliferation of CD8 cytotoxic T lymphocytes and increase the relative rate of CD4 Th2 lymphocytes[97,100]

Inhibit the maturation of monocytes into dendritic cells[94]

Inhibit the secretion of TNF-α, INF-γ, and IL-12 by dendritic cells and increase their secretion of IL-10, reducing the proinflammatory potential[95]

Suppress the proliferation, cytolytic activity, and cytokine secretions of the NK cells[96]

Express indoleamine 2,3-dioxygenase upon INF-γ stimulation, leading to tryptophan depletion and the inhibition of T-cell proliferation[98]

MSCs in liver fibrosis

Reduce the proliferation of HSCs and the synthesis of collagen type I through the secretion of TNF-α[125]

Induce HSCs apoptosis[124]

Express matrix metalloproteinase-9, which degrades the extracellular matrix[128,129]

MSCs in liver regeneration

Secrete trophic factors (HGF, EGF, and IGF-1) that promote hepatocyte proliferation and function during liver regeneration[68,128,130]

EGF: Epidermal growth factor; HGF: Hepatocyte growth factor; HSC: Hepatic stellate cell; IGF-1: Insulin-like growth factor-1; IL: Interleukin; INF-γ: Interferon-γ; MSC: Mesenchymal stem cell; TNF-α: Tumor necrosis factor-α.

MSC TRANSPLANTATION: A PROMISING STRATEGY TO TREAT PATIENTS WITH ALD

Multiple mechanisms have been suggested to play a role in amelioration of liver diseases after MSC administration, such as: trans-differentiation of MSCs into hepatocytes, immunomodulation, inhibition of fibrosis development, protective effects on hepatic cells, and restoration of hepatic cell proliferation capacity (Figure 1).

Figure 1 Pathogenesis of alcoholic liver disease and possible interventions of mesenchymal stem cells. Ethanol promotes the translocation of lipopolysaccharides from the gastrointestinal lumen to the portal vein. In Kupffer cells and in HSCs, lipopolysaccharides increase the expression of multiple pro-inflammatory cytokines, reducing liver regeneration. Chronic alcohol exposure reduces the intracellular concentration of antioxidants with subsequent mitochondrial dysfunction, leading to hepatocyte apoptosis. Acetaldehyde is highly toxic to hepatocytes because it binds to proteins forming adducts that promote glutathione depletion, lipid peroxidation, and mitochondrial damage. Additionally, these adducts act as antigens that activate the adaptive immune response, leading to lymphocyte recruitment to the liver. HSCs can be activated by damaged hepatocytes and activated Kupffer cells through various profibrogenic mediators, resulting in ECM accumulation and fibrosis. The interventions of MSCs include: (1) trans-differentiation into parenchymal cells; (2) induction of endogenous regeneration (i.e., stimulation of hepatocyte proliferation, inhibition of hepatocyte apoptosis, and improvement of the impaired endogenous regeneration); (3) modulation of inflammation (i.e., inhibition of APC maturation, proliferation, activation, and/or T-cell priming activity, reduction of lymphocyte proliferation and stimulation of Treg proliferation); and (4) decrease of liver fibrosis (i.e., inhibition of HSC proliferation, stimulation of HSC apoptosis and induction of ECM degradation). APC: Antigen-presenting cell; ECM: Extracellular matrix; HSC: Hepatic stellate cell; MSC: Mesenchymal stem cell; ROS: Reactive oxygen species; TGF-β: Transforming growth factor-β.

Differentiation of MSC into parenchymal cells

The high degree of plasticity of MSCs has been widely described over the last decade or so[55,71]. Thus, MSCs have the potential cross the germ line barrier and differentiate into non-mesodermal cells (such as hepatocytes and neurons)[72]. It is important to note that MSC-derived hepatocytes need to not only express the genes found in mature liver cells, but express them at a level that is close to what is observed in the normal liver. Therefore, it is crucial to define which characteristics are needed for a differentiated cell to be comparable to a primary hepatocyte. The minimal set of functions of a true hepatocyte includes: (1) metabolic function (detoxification of xenobiotics and endogenous substances); (2) synthetic function (production of albumin, clotting factors, and complement); and (3) storage function (storage of glycogen and fat-soluble vitamins)[73].

Although the protocols for hepatocyte induction have been standardized for cultured MSCs[74,75], an organ-specific microenvironment is the most suitable place for them to differentiate into the required cell types. In this sense, Sato et al[76] were the first to demonstrate the in vivo hepatic differentiation potential of hMSCs. In this study, hMSCs were directly xenografted to the liver of allyl alcohol-treated rats, and they observed that some of the administered hMSCs differentiated into hepatocyte-like cells one month later. Additionally, the in vivo hepatic differentiation potential of MSCs has been demonstrated in rats[77], mice[78], sheep[79], and humans[51].

On the other hand, in vitro differentiated cells were found to express hepatocyte markers (alpha-fetoprotein, albumin, CK18, CK19, CYP1A1, CYP3A4, G6P, and human growth hormone-releasing factor)[80], store glycogen[81], clear ammonia and produce urea[82], and to secrete albumin and uptake low-density lipoprotein[83,84]. However, it is much more challenging to determine whether a cell is a true hepatocyte in vivo. Immunostaining for albumin, CK18, or hepatocyte nuclear factor are recognized indicators of hepatocyte trans-differentiation but not cellular functionality. It is important to note that differentiated MSCs still express mesenchymal markers such as CD90, α-smooth muscle actin, vimentin, and fibronectin, suggesting that complete trans-differentiation is not achieved[85].

Hepatic trans-differentiation potential is essential for MSCs-based therapies in the context of ALD, in which the injured hepatocyte cannot regenerate. However, the initial optimism has been tempered by the recognition of many groups that fusion of MSCs with endogenous hepatocytes is the main mechanism by which new hepatocytes are produced in vivo[86,87]. Hence, irrespective of whether the mechanism is MSC trans-differentiation or fusion, these events do not occur at a sufficiently high frequency to account for the observed functional improvement after MSC administration. Therefore, additional mechanisms may be involved in the regenerative process[88-90].

Modulation of inflammation by MSCs

Liver injury caused by persistent inflammation is accompanied with T cell, B cell and monocyte infiltration of the liver[91,92]. In this respect, MSC immunomodulatory and immunosuppressive properties could potentially be involved in the positive effects that MSC transplantation has in chronic and acute liver diseases.

MSCs regulate the activity of cells from both adaptive and innate immunity[93]. In vitro, they inhibit the differentiation of monocytic precursors into activated dendritic cells[94,95]. Thus, MSCs indirectly limit the cytotoxic expansion and activity of NK T lymphocytes[96]. Both in vitro and in vivo, MSCs downregulate the expression of proinflammatory molecules [interleukin (IL)-1β, IL-12, TNF-α, and interferon-γ] and secrete anti-inflammatory factors (IL-4 and IL-10), shifting the immune response pattern toward a protective Th2 type, and establishing a tolerogenic microenvironment where activated T cells are unable to proliferate and die by apoptosis[97].

Another candidate for the suppressive effects of MSCs is indoleamine 2,3-dioxygenase, which is expressed by MSCs upon interferon-γ stimulation, leading to tryptophan depletion, and thus inhibition of T-cell proliferation[98]. This effect on T lymphocytes indirectly suppresses the function of B lymphocytes because their activation is mainly T-cell dependent. Moreover, MSCs can also modulate B-cell functions by inhibiting their proliferation, differentiation into antibody-secreting cells, and chemotaxis[99].

MSCs also promote the appearance of regulatory T cells, inducing antigen-specific tolerance[100]. Interestingly, it has been shown that the immunologic properties of undifferentiated MSCs are retained when they differentiate into parenchymal cells[101]. Therefore, both undifferentiated and differentiated MSCs will contribute to the maintenance of a microenvironment that allows tissue regeneration.

Induction of endogenous regeneration by MSCs

It is known that MSCs have the ability to secrete, in vitro and in vivo, a wide range of trophic factors, including VEGF, basic fibroblast growth factor, HGF, platelet-derived growth factor, TGF-β, IGF-1, and EGF[68]. The biologic effects of these factors can be both direct, by unleashing intracellular signalization pathways, and indirect, by inducing other cells from the microenvironment to secret additional bioactive factors. Therefore, it has been proposed that MSCs have a catalytic role in tissue regeneration, as once in the damaged tissue, they are able to modify the microenvironment by secreting factors that would: (1) prevent parenchymal cells from dying; (2) induce the proliferation and differentiation of endogenous progenitors; (3) promote neovascularization; and (4) avoid/revert fibrosis development[88,90].

Diverse studies have shown that < 1% of systemically administered MSCs are still present in any organ, including the lung, heart, kidneys, liver, spleen, and gut, one week after administration[102-104]. However, clinically, the beneficial effects associated with MSC administration can be observed for much longer than one week.

MSC-conditioned medium (MSC-CM) administration can recapitulate the beneficial effects of MSCs regarding tissue repair; for instance, data from van Poll et al[105] has provided the first clear evidence that MSC-CM procures trophic support for injured liver by inhibiting hepatocellular death and by stimulating liver regeneration. Although no specific mechanisms of action have been identified, soluble factors, including VEGF, HGF, IGF-1, EGF, IGF-binding protein, and IL-6, have been implicated in those regenerative effects.

Microvesicles (MVs) have recently been considered as important mediators of cell-to-cell communications, as they carry a complex load of proteins, lipids, mRNA, and microRNA, which might affect several cellular processes and pathways[106]. MVs account for approximately 10% of conditioned medium components in terms of protein amount; therefore, MSC-CM therapeutic activity could thus be partially attributed to MVs[107,108].

In addition to the induction of liver regeneration, antifibrotic properties of the MSC secretome have also been described. In this sense, Li et al[109] demonstrated that transplantation of MVs derived from human umbilical cord MSCs can alleviate liver fibrosis induced by carbon tetrachloride administration. These results have also been recapitulated by the administration of ex vivo expanded MSCs[109-112]. However, other studies have reported that MSCs can potentially be fibrogenic and contribute to increased fibrosis[113-115] or have no effect whatsoever[116,117].

These experimental results suggest two apparently contradictory scenarios; a great number of variables contribute to the inconsistences between the different observations. One such inconsistency is the difference in the properties of MSCs prepared in different laboratories, due to differences in the protocols used for MSC isolation and ex vivo expansion. There are also important differences between hMSCs and rodent MSCs, and even between different mouse strains[55]. Finally, another important factor is the dependence of the MSC differentiation process on most of the culture conditions or in vivo microenvironments, especially those developed in damaged tissue. In most of the cases, the signals that drive this differentiation process have not been characterized, so they cannot be replicated in vitro.

MSC TRANSPLANTATION IN ANIMAL MODELS OF LIVER INJURY

Numerous studies have tried to demonstrate the therapeutic potential of MSCs in the treatment of acute and chronic liver diseases, however, to date, a gap in the study of MSC administration for the treatment of ALD remains (Table 2). This gap is due, in part, to the lack of experimental animal models that recapitulate the full progression of ALD in human patients. Nonhuman primates are possibly the most similar model for human diseases[118,119]. For example, exposure of baboons to ad libitum alcohol intake leads to the progression of all stages of liver damage associated with ALD in humans. However, the relevance of nonhuman primates as a model of ALD is outweighed by the prodigious cost of maintaining them, which limits their utility to the field as a whole. Therefore, it is not surprising that the majority of alcohol research performed in animal models involves rodents[118,119]. The major disadvantage of rodent models with regard to experimental ALD is that the obtained liver pathology is limited predominantly to steatosis, with some necroinflammatory changes. The more-severe steatohepatitis and advanced liver damage observed in human patients (fibrosis and cirrhosis) is generally not observed in rodents[118,119].

Table 2 Preclinical studies using mesenchymal stem cells or their derivatives to treat liver injury.

Model animal species	Liver injury induction/kind of liver injury	MSCs administration route	Number andsource of transplanted MSCs	Therapeutic effect	Proposed mechanisms	Ref.
Rat	Allyl alcohol (ip administration)/chronic damage	Intrahepatic	1 × 106 MSCs from human BM	Hepatocyte regeneration	Hepatocyte differentiation without evidence of cell fusion	[76]
Mouse	Low-level of radiation/minimal, hepatic damage	Tail vein	2 × 104 MSCs from mouse BM	Hepatocyte regeneration	Hepatocyte differentiation	[78]
Mouse	Chronic exposure to high fat diet/NASH	Tail vein	0.5 × 106 MSCs from mouse BM	Prevention of NASH onset	Paracrine promotion of hepatic proliferation	[110]
				Preclusion of the inflammatory process	Increase in the fatty-acid oxidation enzymes expression
Mouse	Chronic exposure to atherogenic diet/NASH	Splenic capsule	0.1 × 106 MSCs from mouse adipose tissue	Restoration of albumin expression in hepatic parenchymal cells	Modulation of inflammation	[111]
				Amelioration of fibrosis	Increase in MMP expression
				Suppression of persistent hepatic inflammation
Mouse	CCl4 (ip administration)/liver fibrosis	Spleen	0.5 × 106 MSCs from human amniotic membrane	Reduction of liver fibrosis	Inactivation of HSCs	[126]
				Improvement of hepatic function	Reduction of hepatocyte apoptosis
					Promotion of liver regeneration
					Differentiation of hepatocyte-like cells
Mouse	CCl4 (ip administration)/liver fibrosis	Tail vein	0.5 × 106 MSCs from human BM	Reduction of liver fibrosis	Induction of MMP-9 expression	[121]
					Reduction in TGF-β expression
Rat	D-galactosamine (ip administration)/fulminant hepatic failure	Penile vein	Conditioned medium from human BM MSCs	Reduction in the mortality rate	Modulation of the immune response	[105,122]
				Reduction in panlobular leukocyte infiltrates	Trophic factor release (i.e., VEGF, HGF, and IGF-BP)
				Reduction in hepatocellular death
Mouse	CCl4 (ip administration)/liver fibrosis	Intrahepatic	Exosomes derived from human umbilical cord MSCs	Recovery of serum aspartate aminotransferase activity	Not determined	[109]
				Decrease in collagen type I and III, TGF-β1 level

BM: Bone marrow; HGF: Hepatocyte growth factor; HSC: Hepatic stellate cell; IGF-BP: Insulin-like growth factor-binding protein; ip: Intraperitoneal; MMP: Matrix metalloproteinase; MSC: Mesenchymal stem cell; NASH: Nonalcoholic steatohepatitis; TGF-β: Transforming growth factor-β; VEGF: Vascular endothelial growth factor.

Several in vivo studies have been performed to evaluate the therapeutic potential of MSCs in the context of liver fibrosis[54,56]. In most of the studies, liver fibrosis was induced by intraperitoneal or subcutaneous injection of carbon tetrachloride, however, this model cannot provide a perfect simulation of human etiology[120,121].

Application of MSCs in the in vivo models of liver fibrosis/cirrhosis ameliorates the development of the disease[54,56,111,112]. Similar results were obtained when MSC-CM or MVs were applied[105,108,109,122], suggesting that long-term survival of MSCs might not be necessary for their beneficial effects. In these studies, the reduction of fibrosis was correlated with the decrease in the synthesis of collagen I and matrix metalloproteinase inhibitors, with a concomitant decrease in activated HSCs. Multiple mechanisms have been suggested to participate, such as immunomodulation[123], selective apoptosis of[124,125] or reversion to a quiescent state of HSCs, and production of protective factors[126,127].

Studies of in vitro co-cultures of MSCs with activated stellate cells have shown that, even in small numbers, MSCs can paracrinally inhibit the fibrogenic activity of activated stellate cells. This inhibition can be a consequence of the secretion of IL-10 and TNF-α by MSCs. Moreover, MSCs are able to induce apoptosis in reactive stellate cells, a process mediated in part by the secretion of HGF[125]. These results support the hypothesis that the therapeutic effects of MSCs on fibrosis inhibition are the result of the secretion of paracrine factors that modulate the proliferation, viability, and function of resident stellate cells. The production of matrix metalloproteinases can also be effective at reverting hepatic fibrosis. MSCs are capable of secreting and inducing the expression of matrix metalloproteinase-9 and -13 in other cells, the latter being the main rodent and human interstitial collagenase[128,129].

In ALD, as well as in more prominent cirrhotic liver, hepatocytes are reported to have reduced proliferative capacity, which may reflect either the inhibitory effect of adjacent collagen I or that they have reached replicative senescence after many rounds of injury and repair[44,45]. MSC infusion may increase the intrinsic ability of hepatocytes to proliferate by the release of proliferative trophic factors and cytokines, or by facilitating the breakdown of scar tissue, thereby removing a block to proliferation[130].

In our laboratory, we found that intravenous administration of bone marrow-derived MSCs into animals suffering from diet-induced metabolic syndrome and obesity restores liver function and avoids progression from steatosis to nonalcoholic-steatohepatitis[110]. Such MSC-mediated hepatoprotection was unrelated to metabolic syndrome reversion. Nevertheless, this has been associated with the potential of MSCs to enhance liver regeneration and/or manage the second hit required for the transition from steatosis to nonalcoholic-steatohepatitis, as an increased hepatic proliferation rate was found as well as an increased expression of fatty-acid oxidation enzymes. Thus, MSC administration could prevent the progression of ALD by reducing the impairment of fatty-acid oxidation.

Finally, the question of the ideal route of MSC injection remains one of the main unsolved issues regarding efficient administration of MSCs. Even if the tail vein seems to be the most often used administration route in animals, the portal vein and intrahepatic injections also seem to be efficient[129,131]. The optimal dose of cells or conditioned medium also needs to be evaluated because there are significant variations among studies in terms of the number of cells injected per animal.

CLINICAL TRIALS USING MSCS

MSCs have been successfully used in humans to treat different pathologies such as osteogenesis imperfecta[132], idiopathic aplastic anemia[133], graft-versus-host disease[134], and acute myelogenous leukemia[135]. Other applications have been to specifically avoid lung fibrosis injury after bleomycin challenge[136], and for the protection of cardiac function after a myocardial infarction[137]. In every case, clear therapeutic effects with no complications have been reported.

In the same direction, the translation of preclinical research on MSCs to clinical use for cirrhotic patients has generated great interest due to the growing population of patients with advanced liver diseases and the critical shortage of available liver donors.

To date, some clinical trials using hMSCs to treat patients with liver fibrosis have been published[112,138-145]. Unfortunately, in general, the studies were heterogeneous in their design and did not distinguish between the various etiologies of cirrhosis. ALD patients and viral hepatitis patients were mixed together in small case series.

Recently, Jang et al[140] evaluated the effect of autologous bone marrow-derived MSC transplantation on hepatic fibrosis in patients with alcoholic cirrhosis. After MSC administration, liver histologic improvements were observed in 6/11 patients, and recovery of liver function in 10 patients associated with a decreased expression of TGF-β1, collagen type I, and α-smooth muscle actin, without significant complications or side effects during the study period[140]. These results support the use of these cells as a therapy for patients with alcoholic cirrhosis. However, further prospective, controlled studies are needed before MSC administration can be accepted as new strategy for antifibrosis therapy.

POTENTIAL LIMITATIONS TO CLINICAL TRANSLATION

Knowledge regarding MSC biology and their application in liver fibrosis treatment has significantly increased over the past years. Nevertheless, the clinical use of MSCs for liver regeneration, in particular ALD, is still in its beginnings, and fundamental questions remain to be addressed.

Although clinical trials have provided hope that MSCs could be a valuable resource for cell-based therapies for liver fibrosis, these results must be interpreted with some caution given the limited number of patients enrolled in each trial and the lack of appropriate controls. For example, patients with acute alcoholic hepatitis normally receive a high dose of prednisone therapy. However, the effect of high-dose steroids on the transplantation of MSCs is not well studied. There is some evidence that MSCs are glucocorticoid sensitive and are induced to differentiate into adipocytes with steroid exposure[146].

Clinical trials have shown that MSC-based therapy is relatively safe, and no serious detrimental effects have been reported in humans to date. However, some concerns have risen over the use of replicating cells, which may escape control as time elapses[147]. Some potential complications could also arise from intravascular administration of MSCs leading to vascular occlusion. Preclinical studies have not excluded the differentiation of injected MSCs into ectopic structures[148], myocardial calcification[149], and enhanced accumulation of fibroblasts and myofibroblasts in the lungs[150], as these events have been reported following MSC treatment.

CONCLUSION

Stem cell-based therapy represents a newly emerging therapeutic approach to treat ALD. MSCs are an attractive tool because they have been shown to trigger the regeneration of damaged liver tissue, with no evidence of significant adverse effects in either preclinical or clinical studies.

Due to the relation between pathologic events that occur in ALD development and the cellular and molecular mechanisms associated with MSC therapeutic effects, we believe that MSC transplantation could be a promising therapeutic strategy to manage ALD progression.

ACKNOWLEDGMENTS

The authors thank Dr. Amelina Albornoz for the English editing of the manuscript.