In vivo/in vitro or disease models | Type of stem cells | Involving factors | Outcome | Ref |
---|---|---|---|---|
Rat’s acute lung injury | BM-MSCs | Downregulation of inflammatory factors: VEGF, NF-ƘB, and IL-17A | Alleviating lung injury | [152] |
Repairing of alveolar type II epithelial cells | ||||
Lung progenitor organoid cultures | BM-MSCs | Increasing the number of Epcam + Sca-1 + distal lung epithelial cells | Increased alveolar differentiation to tissue repair | [153] |
COPD patients' tissue-derived organoids/A549 cell line | Lung derived MSCs | Downregulation of TGF-β and WNT-5A | Induce generation of alveolar organoids | [154] |
Attenuates alveolar epithelial injury | ||||
Trigger Epithelial repair | ||||
Rat myocardial infarction model | BM-MSCs | Increasing the expression of TGF-β, FGF-2, angiopoietin-2, VEGF-1 | Increase in angiogenesis rate | [155] |
Induces myocardial regeneration and cardiac function | ||||
The 4-week-old female New Zealand white rabbits injured endometrium model | BM-MSCs | Increasing CK-19 expressions | Regulate repair of injured endometrium | [156] |
Upregulation of TGF-β1, TGF-β1R, and Smad2 mRNA | Enlarging the number of glands of the endometrial damaged uterus | |||
Downregulation of the expression of TGF-β1 and Smad2 mRNA | Reducing e fibrosis area of the endometrial damaged uterus | |||
Culture of human iPSC-MSCs Bowel disease models in mice | iPSC-MSCs | Multiplying the frequency of CD44+ cells and CBC stem cells (Lgr5+ cells) in colonoids | Promote crypt epithelial cell proliferation via TSG-6 | [157] |
The expression and secretion of TSG-6 before the coculture with colonoids | ||||
Mice DSS (dextran sulfate sodium)-induced colitis model | ESC-MSCs | Decrease of CXCL1, CXCL2, IL-6, and MCP-1 significantly | Ameliorate colon epithelial proliferation and integrity | [158] |
Reducing epithelium loss and inflammatory cell infiltration | Encourage the colon epithelial integrity and regeneration | |||
Increase of IGF1R, p-IGF1R, AKT, and p-AKT in the treatment group | ||||
Sprague–Dawley rats cutaneous wound healing models | HucMSCs | Increasing B-catenin and its downstream genes (cyclin-D1, cyclin-D3, and N-cadherin) | Promote wound closure of reversible scratches with concomitant treatment | [159] |
The induction of b-catenin downstream genes (cyclin-D1, cyclin-D3, and N-cadherin) | Upgrade the phosphorylation of GSK3b and inhibited the activity of GSK3b |