Copyright
©The Author(s) 2021.
World J Stem Cells. Oct 26, 2021; 13(10): 1549-1563
Published online Oct 26, 2021. doi: 10.4252/wjsc.v13.i10.1549
Published online Oct 26, 2021. doi: 10.4252/wjsc.v13.i10.1549
Ref. | Animal model (species, age, n number) | ED model | Evidence of previous DE | Type of stem cell | Source of stem cell | Characterization of stem cell | Number of cells injected and site of injection | Modification | Duration of follow-up | Parameter of therapy | Conclusion |
Garcia et al[68] | 10-wk-old Zucker (fa/fa) rats; n = 10 in each group (ADSCs and control) | Obese and type 2 diabetic rats with ED | Yes, CN electrostimulation | ADSCs; Autologous | Perigonadal adipose tissue | Not clear | 1 × 106/IC | None | 3 wk | ICP-MAP, nNOS, corporal body collagen, and corporal body endothelial cell | ADSCs improve ED |
Liu et al[57] | 10-wk-old male Sprague-Dawley rats; n = 12 in each group (lentivirus-VEGF, GFP ADSCs, VEGF/GFP ADSCs, control) | Type 1 diabetes induced by streptozotocin with ED | Yes, APO procedure | ADSCs; Allogenic | Bilateral groin | Yes, by flow cytometry | 1 × 106/IC | VEGF, GFP | 3 wk | ICP-MAP, VEGF, and e-NOS in vivo Endothelial, smooth muscle, and pericyte marker | Injection of ADSCs expressing VEGF displayed more efficiently and significantly raised ICP-MAP and increased endothelial markers |
Ouyang et al[55] | Male Sprague-Dawley rats unspecific age; n = 10 in control group, n = 15 in each treatment group (USCs, lentivirus FGF2, USCs-FGF2) | High-fat diet following streptozotocin-induced diabetes | Yes, APO procedure | HUDSCs | Human urine | Yes, flow cytometry (CD24, CD29, CD31, CD34, CD44, CD45, CD73, CD90, CD105, CD146) | 1 × 106/IC | FGF-2 | 4 wk | ICP-MAP, expression of endothelial markers (CD31, VEGF, and eNOS), smooth muscle markers (desmin and smoothelin), histological changes | USCs or USCs-FGF2 improved erectile function in type 2 diabetic rats |
Li et al[69] | 8-wk-old BALB/c mice; n = 8 in each group (control and treatment) | Streptozotocin-induced diabetes with ED | Not clear | BMSCs; Allogenic | Unspecified bone marrow | Yes, by flow cytometry. Identification with Sca-1 micromagnetic, identification of CD29, CD44, CD13, and CD34 | Not mentioned | None | 3 wk | ICP-MAP, penile histology | Flk-1 Sca-1 MSCs differentiate into skeletal and endothelial cells in vivo and in vitro |
Liu et al[45] | Male Sprague-Dawley rats with no mentioned age; n = 10 in each group (negative control, ADSCs, ADSCs + hepatocyte growth factor) | Streptozotocin-induced diabetes with ED | Not clear | ADSCs | Not mentioned | Yes | 2 × 106/IC | Hepatocyte growth factor | 4 wk | ICP-MAP, smooth muscle, and endothelium (PECAM-1, SMA), apoptotic index | Significantly enhance the erectile function |
Wang et al[70] | 10-wk-old Male Sprague-Dawley rats; n = 15-16 in each group (control, normoxia AMCS, and hypoxia AMCS) | Streptozotocin-induced diabetic mouse | Yes, APO procedure | ADSCs; Allogenic | Inguinal adipose | Yes, fluorescent-activated cell sorting (CD90, CD29, CD34, CD45) | 1 × 106/IC | Normoxia-hypoxia | 4 wk | ICP-MAP, n-NOS, endothelial and smooth muscle histology | Hypoxia AMSCs improved ICP-MAP, nNOS. Hypoxia AMSCs condition effective to enhance theuraphetic effect of ED |
Kovanecz et al[71] | 7-mo-old Zucker (fa/fa) rats; n = 8 in each group (untreated, early diabetic treated with SC, early diabetic with high glucose treated with SC, late diabetic treated with SC, non-diabetic untreated) | Not mentioned specifically | Not clear | MSDCs; Allogenic | Hindlimb muscles | Not clear | 1 × 106/IC | Early and late diabetes | 8 wk | ICP-MAP, nNOS-eNOS, collagen ratio, calponin, inflammation marker | Stem cell decreased collagen and fat infiltration, upregulated nNOS-eNOS, and improved erectile function |
Ryu et al[46] | 12-wk-old C57BL/6J mice; n = 6 in each group (control, diabetic, diabetic with PBS, and diabetic with BMSCs) | Streptozotocin-induced diabetic mouse | Not clear | BMSCs; Allogenic | Tibiae and Femur | Yes, flow cytometry (CD3, CD44, CD45, CD103, CD105, CD117, MHC-1, and Sca-1) | 3 × 105/IC | None | 2 wk | e-NOS-nNOS, endothelial and smooth muscle content histology | BMSCs improved significant recovery of erectile tissue |
Zhou et al[48] | 8-wk-old male Sprague-Dawley; n = 5 in each group (negative control, ASCs + ad-luc-myocardin, ASCs + ad-luc, ED without treatment) | Streptozotocin-induced diabetic mouse | Not clear | ADSCs; Autologous | Paratesticular fat tissue | Not clear | 1 × 106 ADSC/IC | Insulin and neutral protamine hagedorn | 4 wk | ICP-MAP, AGEs, and RAGE; growth factors and cytokine in penis | ADSCs combined with insulin improved erectile function and pathological changes |
Wang et al[52] | 10-wk-old male Sprague-Dawley rats; n = 14-15 in each group (negative control, icariin, ADMSCs, ADMSCs + icariin) | Streptozotocin-induced diabetic mouse | Yes, APO procedure | ADSCs; Allogenic | Inguinal adipose | Yes, fluorescent-activated cell sorting (CD90, CD29, CD34, CD45) | 1 × 106/IC | Icariin | 4 wk | ICP-MAP, histology and immunohistology of penis tissue, intracellular ROS levels | Icariin-enhanced ADSCs in erectile function Icariin could protect ADSCs against oxidative stress |
Zhou et al[50] | 8-wk-old male Sprague-Dawley rats; (n = 8 in control, n = 20 in treated groups) | Streptozotocin-induced diabetic mouse | Yes, APO procedure | ADSCs; Allogenic | Paratesticular fat tissue | Not clear | 1 × 106 ADSC and 1 × 104 ADSCs per MT/IC | Microtissues (MTs) | 4 wk | ICP-MAP, nNOS, smooth and endothelial content histology | MTs improved histopathology and erectile function rather than traditional ADSC |
Zhu et al[49] | 10-wk-old male Sprague-Dawley rats; n = 8-10 in each group (non-diabetic controls, diabetic with PBS, ADSCs, ADSCs + Magnetic application | Streptozotocin-induced diabetic mouse | Not clear | ADSCs; Autologous | Paratesticular fat tissue | Yes, by flow cytometry (CD34, CD45, CD44) | 1 × 106 ADSC | Magnetic iron oxide nanoparticle | 4 wk | ICP-MAP, contents, smooth muscle (α-SMA), endothelium (von Willebrand factor), VEGF | ADSCs improved erectile function External magnetic field improved efficiency of labeled ADSC in the corpus cavernosum |
Jeon et al[56] | 8-wk-old male Sprague-Dawley rats; n = 12 in each group (control, DM ED, BM-MSC, SDF-1 (stromal cell-derived factor-1) | Streptozotocin-induced diabetic with ED | Not clear | BMSCs | Not mentioned | Not mentioned | 1 × 106/IC | SDF-1 | 4 wk | ICP-MAP, nNOS-eNOS, FGF-VEGF in vivo | SDF-1 improved ED recovery and smooth muscle content, increased nNOS-eNOS, FGF-VEGF |
Chen et al[42] | Male Sprague-Dawley rats with unspecific age; n = 10 in each group (ADSC, BMSC, and control) | ED in type 2 rats with diabetes induced by high-fat and high-sugar diet and streptozotocin | Yes, by APO procedure | ADSCs and BMSCs; Allogenic | Medullary cavity of femur, tibia, and fibula | Yes, by flow cytometry Identification with CD34,CD45,CD73,CD90, and CD105 | 1 × 106/IC | None | 2 wk | ICP-MAP, number of blood vessels, collagen | Stem cell improved ICP-MAP, increased the number of blood vessels, and reduced collagen content |
Ouyang et al[72] | Male Sprague-Dawley rats with unspecific age; n = 8 in each group (control and treatment) | Streptozotocin-induced diabetes | Yes, APO procedure | HUDSCs | Human urine | Yes, flow cytometry and Western blot (CD63 and protein calnexin) | Not mentioned | None | 4 wk | ICP-MAP, eNOA, phospho-eNOS, nNOS, and endothelial markers (CD31) | Human-derived stem cells improved ICP, eNOS, nNOS, and endothelial markers |
Zhang et al[51] | Male Sprague-Dawley rats; n = 10 in each group (negative control, ASCs + ad-luc-myocardin, ASCs + ad-luc, ED without treatment) | Streptozotocin-induced diabetic mouse | Yes, APO procedure | ADSCs; Allogenic | Inguinal fat tissue | Yes, flow cytometry (CD29, CD90, CD34, and CD45) | 1 × 106/IC | Ad-luc-myocardin modified | 3 wk | ICP-MAP, collagen and smooth muscle histology: myocardin, collagen 1, cleaved caspase 3, α-SMA, and calponin | Myocardin enhanced therapeutic for ASCs for ED in diabetic mouse |
Zhang et al[58] | CCECs culture, not specific rats; n = 15 each group (case and control) | CCECs treated with advanced glycation end products and streptozotocin-induced diabetic mouse | In vivo CCECs mimicking diabetic and APO procedure | HUDSCs | Human urine | Yes, by flow cytometry (CD24, CD31, CD34, CD44, CD45, CD73, CD90, CD105) | Not mentioned | None | 4 wk | ICP-MAP, eNOS, p-NOS, VEGFRA, VEGFR2, authophagic flux | Urine stem cell improved cavernosal endothelium through upregulated authophagic activity |
Zhang et al[47] | 8-wk-old male Sprague-Dawley rats; n = 9 in each group (control group, DM with ED, ADSCs, ADSCs-EFGP, ADSCs + iNOS) | Streptozotocin-induced diabetic mouse | Yes, APO procedure | ADSCs; Allogenic | Inguinal fat tissues | Yes, by flow cytometry (CD2, CD31, CD49, CD90, CD106, CD34, CD45, CD73) | 5 × 105/IC | EFGP and iNOS | 2 wk | ICP-MAP, endothelial and smooth muscle content marker (NO, collagen-I, collagen IV, TGF-β, β- actin) | ADSCS-iNOS significantly reduced penile fibrosis |
Song et al[54] | Male Sprague-Dawley rats; n = 7-8 in each group (BMSC-EXO, ADSC-EXO, CCSMC-EXO, control) | Streptozotocin-induced diabetic mouse | Yes, APO procedure | ADSCs and BMSCs; Allogenic | Inguinal adipose and rat femoral | Yes, flow cytometry (CD29, CD34, CD45, and CD90 | 100 μg of exosome/IC | Exosome CCSMC | 4 wk | ICP-MAP, α-SMA collagen, TGF-β1, β-actin, e-NOS, and n-NOS, NO, and cGMP | CCSMC-EXOs improve erectile function, reducing collagen deposition and expression of eNOS-nNOS, NO, and cGMP |
Wang et al[53] | Male Sprague-Dawley rats with unspecified age; no data on n number, four experimental groups in total (negative control, DM, DM + ADSC-EXO, DM + siCorin-ADSC-EXO) | Streptozotocin-induced diabetic mouse | Yes, but not mention what method | ADSCs; Allogenic | Not Mention | Yes, CD29, CD90, CD44, CD105, and von Willebrand factor | 100 μL of exosome from ADSCs/IV | siCorin ADSC-EXO | 2 wk | ICP-MAP, neurovascular function (ANP, BNP, nNOS, cGMP, β-actin) , inflammatory factor (IL6, IL1β), expression, delivery of corin | ADSC-EXO enhanced endothelial recovery and decreased inflammatory process |
Ref. | Study subject and n number | Type of ED | Evidence of previous DE | Type of stem cell | Source of stem cell | Stem cell characterization | Number of cells injected and site of injection | Modification | Duration of follow-up | Parameter of therapy | Conclusion |
Bahk et al[61] | Impotent diabetic type 2 patients range from 57 yr to 87 yr; n = 7 in treated groups, n = 3 in controls. | Diabetic ED | Yes, by clinical diagnosis and other parameters | UCBSCs; Allogenic | Umbilical cord | Yes, by flow cytometry (CD13, CD14, CD34, CD31, CD45, CD44, CD49e, CD54, CD90, CD106, and HLA-DR) | 1.5 × 107/IC | None | 9 mo | IIEF-5, SEP, GAQ, erection diary, blood glucose diary | Umbilical cord blood stem cell had positive effects on ED |
Levy et al[59] | Men aged 40-70 yr who had organic ED at least 6 mo; n = 8 | Diabetic ED | Yes, by clinical diagnosis and other parameters | PM-MSCs; Allogenic | Placenta | Not clear | 1 mL PM-MSCs /IC | None | 6 wk, 3 mo, 6 mo | Peak systolic velocity, end-diastolic velocity, stretched penile length, penile width, IIEF-5 | The treatment may be beneficial |
Al demour et al[60] | Men aged 25-65 yr who had ED at least 6 mo; n = 4 | Diabetic ED | Yes, by clinical diagnosis and other parameters | BMSCs; Autologous | Iliac crest | Yes, positive for CD90, CD105, CD73, and CD44 | 15 × 106/IC | None | 2 yr | IIEF-5, EHS | Stem cell effective and improved erectile function |
Protogerou et al[62] | Male with ED due to DM, hypertension, hypercholesterolemia, and Peyronie’s disease; n = 5 in each group (control and ADSC treated) | Diabetic ED | Yes, by clinical diagnosis | ADSCs; Autologous | Not mentioned | Yes, alizarin red S and alcian blue staining, flow cytometry | 2 × 105/IC | None | 3 mo | IIEF-5, penile triplex | No difference in IIEF-5 between the case and control group, but significant between before and after treatment in both groups |
- Citation: Pakpahan C, Ibrahim R, William W, Faizah Z, Juniastuti J, Lusida MI, Oceandy D. Stem cell therapy and diabetic erectile dysfunction: A critical review. World J Stem Cells 2021; 13(10): 1549-1563
- URL: https://www.wjgnet.com/1948-0210/full/v13/i10/1549.htm
- DOI: https://dx.doi.org/10.4252/wjsc.v13.i10.1549