Copyright
©The Author(s) 2021.
World J Stem Cells. Dec 26, 2021; 13(12): 1826-1844
Published online Dec 26, 2021. doi: 10.4252/wjsc.v13.i12.1826
Published online Dec 26, 2021. doi: 10.4252/wjsc.v13.i12.1826
Comparison | Primary MSCs | hPSC-MSCs | Ref. |
Cell number | Limited | Unlimited | [17,36] |
Proliferation | Slower | Faster | [36,39,42,43,48,57] |
Life span | Shorter | Longer | [17] |
Variation | Higher | Lower | [119] |
Differentiation potential | Higher | Lower, esp. adipogenesis | [31,43,47,48] |
Immunosuppression | Higher | Lower | [38,46] |
Pluripotent genes | Lower | Higher | [45] |
Mesenchymal genes | Higher | Lower | [45] |
VCAM1 | Higher | Lower | [44] |
HLA-II | Higher | Lower | [46] |
hPSC-MSCs | Disease model or application | Animal model or human | Therapeutic effects | Ref. |
iPSC-MSCs | CKD | Rat | Protect the kidney against CKD injury | [85] |
iPSC-MSCs | Adriamycin nephropathy | Mouse | Prevent adriamycin nephropathy | [82] |
iPSC-MSCs | Obesity-associated Kidney injury | Mouse | Ameliorate endoplasmic reticulum stress | [83] |
hPSC-MSCs | UUO | Mouse | Protect against kidney fibrosis in vivo and in vitro | [84] |
hESC-MSCs | LN | Mouse | Prevent the progression of LN | [81] |
iPSC-MSCs | TNBC | Mouse | Significantly decrease the incidence and burdon of metastases | [117] |
iPSC-MSCs | Breast cancer | Mouse | Decrease EMT, invasion, stemness, and growth of cancer cells | [119] |
iPSC-MSCs | Skin wounds, pressure ulcers, and osteoarthritis | Mouse | Have therapeutic potential in skin wounds, pressure ulcers, and osteoarthritis | [127] |
hESC-MSCs | Arthritis | Mouse | Ameliorate collagen-induced arthritis by inducing IDO1 | [72] |
iPSC-MSCs | Osteonecrosis of the femoral head | Rat | Prevent osteonecrosis of the femoral head | [64] |
iPSC-MSCs | Vascularized composite allotransplantation | Rat | Induce T cell hyporesponsiveness to prolong hind limb survival | [106] |
iPSC-MSCs | Limb ischemia | Mouse | Exosomes of iPSC-MSCs attenuate limb ischemia by promoting angiogenesis | [121] |
iPSC-MSCs | Limb ischemia | Mouse | Insensitivity of iPSC-MSCs to interferon γ potentiates repair efficiency of hind limb ischemia | [46] |
iPSC-MSCs | Limb ischemia | Mouse | Attenuate limb ischemia | [35] |
iPSC-MSCs | Periodontal defects | Rat | Aid periodontal regeneration | [68] |
iPSC-MSCs | Bone defects | Mouse | Regenerate non-union bone defects more efficiently than BM-MSCs upon BMP6 overexpression | [33] |
iPSC-MSCs | Calvaria defects | Mouse | Repair calvaria defects | [28] |
iPSC-MSCs | Osteochondral defects | Rat | iPSC-MSCs are able to repair cartilage defects | [17] |
iPSC-MSCs | FOP | FOP-iPSC-MSCs enhance chondrogenesis via activin A enhanced mTOR signalling | [53,54] | |
hESC-MSCs | Lupus and uveitis | Mouse | Increase survival of lupus-prone mice and decrease symptoms of uveitis | [40] |
hESC-MSCs | EAE model of multiple sclerosis | Mouse | Improve EAE symptoms | [101] |
hESC-MSCs | EAE | Monkey | Attenuate disease progression in a primate EAE model | [41] |
hESC-MSCs | EAU | Mouse | Slow down the development of EAU | [103] |
iPSC-MSCs | Inflammatory bowel disease models | Mouse | Promote intestinal repair via TSG-6 | [111] |
hESC-MSCs | Experimental inflammatory bowel disease | Mouse | Protect against experimental inflammatory bowel disease | [107] |
iPSC-MSCs | SS | Mouse | Prevent the progression of SS | [112] |
iPSC-MSCs | Allergic rhinitis | Modulate T-cell phenotypes towards Th2 suppression through inducing Treg expansion | [108] | |
iPSC-MSCs | Asthma Inflammation | Mouse | Alleviate asthma inflammation by CX43-mediated mitochondrial transfer | [110] |
iPSC-MSCs | Corneal injury | Mouse | Exert therapeutic effects in the cornea by reducing inflammation | [99] |
iPSC-MSCs | Skin wound | Rat | iPSC-MSC-Exos improve cutaneous wound healing by promoting collagen synthesis and angiogenesis. | [120] |
iPSC-MSCs | SR-aGvHD | Human | iPSC-MSCs are safe and well tolerated | [114] |
- Citation: Liu TM. Application of mesenchymal stem cells derived from human pluripotent stem cells in regenerative medicine. World J Stem Cells 2021; 13(12): 1826-1844
- URL: https://www.wjgnet.com/1948-0210/full/v13/i12/1826.htm
- DOI: https://dx.doi.org/10.4252/wjsc.v13.i12.1826