Disease | Source | Model | Type of administration | Results | References |
---|---|---|---|---|---|
Multiple sclerosis | ESCs | In vivo | Cell injection | Promote remyelination | [134] |
Ischemic reperfusion injury | IPSCs | In vivo | Intramyocardial (48Â h after reperfusion) | Promote angiogenesis Ameliorate apoptosis and hypertrophy. No effect of infarct size | [135] |
Acute myocardial infarction | IPSCs | In vitro | – | Restore post-ischemic contractile performance, ventricular wall thickness, and electrical stability | [136] |
Myocardial infarction | IPSCs-derived cardiomyocytes | In vivo | Intramyocardial, cell injection | Improve cardiac function | [137] |
Diabetes mellitus | Mouse skin-derived IPSCs | In vivo | Cell injection | IPSCs differentiate into β-like cells, and these could secrete insulin in response to glucose and correct a hyperglycaemic phenotype | [138] |
Parkinson’s disease | IPSCs | In vivo | Cell transplantation | After the transplantation, the cells differentiate into glia and including glutamatergic, GABAergic, and catecholaminergic subtypes. IPSCs were induced to differentiate into dopamine neurons of midbrain character and could improve behavior | [139] |
Stroke | BMSCs | In vivo | Intravenous | Enhance rotarod and adhesive removal | [140] |
Crohn’s disease | Adipose-derived-MSCs | In vitro | – | Impair T helper type-1 cell activation and expansion of CD4+ CD25+ forkhead box (FOX) P3+ T-regulatory cells that suppress T-helper type 1 effector responses | [141] |
Asthma | Human MSCs | In vitro | – | MSCs can suppress proliferation and effector function of CD4+ Th2 cells, Immunoglobulin-E (IgE) production in plasma cells, and IgE-dependent activation of mast cells | [142] |
Systemic lupus erythematosus | Mouse MSCs | In vivo | Tail vein injection | It can suppress Th17. Also, MSCs increase CD4, CD25, FoxP3, and Tregs | [143] |
Lung injury | Mouse MSCs | In vivo | Jugular Vein injection | MSCs support TNF-α oscillation and they alienate the IL-1a function | [144] |
Parkinson diseases | Rat MSCs | In vivo | Intranasal injection | In Parkinson's disease, MSCs reduce inflammatory cytokine secretion | [145] |
Liver fibrosis | Mouse MSCs | In vivo | Tail vein injection | The secretion of MMP-9 and MMP-14 went up. Also, it reduced TGF-β1 | [146] |
Myocardial infarction | Human MSCs | In vivo | Transendocardial injection to pig | They triggered endogenous cardiac stem cells | [147] |
Skin wound | Human MSCs | In vivo | Tail vein injection to mouse | MSCs compress Th17 cells and enhance the expression of IL-10 | [148] |
Corneal abrasion | Mouse MSCs | In vivo | Intravenous and intraperitoneal | MSCs support the production of TSG-6 that is a type of anti-inflammatory protein | [149] |
Rheumatoid arthritis | Human MSCs | In vivo | Intraperitoneal injection to mouse | MSCs can go down the cell effusion of Th1 and Th17, | [141] |
Graft-versus-host disease | Mouse MSCs | In vivo | Intravenous | MSCs reduce TNF-α, IFN-γ, and IL-12 which are a type of inflammatory cytokines | [150] |
Acute lung injury | Mouse MSCs | In vivo | Intravenous | MSCs hinder Th2-moderated allergic airway inflammation | [151] |