Copyright
©The Author(s) 2024.
World J Stem Cells. Jan 26, 2024; 16(1): 7-18
Published online Jan 26, 2024. doi: 10.4252/wjsc.v16.i1.7
Published online Jan 26, 2024. doi: 10.4252/wjsc.v16.i1.7
MSCs | Priming treatments | Model/disease | Therapeutic effects | Ref. |
Priming with inflammatory molecules | ||||
BM-MSCs | IFN-γ | In vivo model of chronic colitis | Attenuation of inflammation | [61] |
UC-MSCs | TNF-α | In vivo model of intrauterine adhesion | Reduction of inflammation and endometrium fibrosis | [62] |
BM-MSCs | IFN-γ | In vivo models of acute radiation syndrome | Protection from radiation-induced lethality | [63] |
UC-MSCs | IL-1β | In vivo model of chronic colitis | Attenuation of inflammation | [64] |
BM-MSCs | IL-25 | In vivo model of chronic colitis | Attenuation of inflammation | [65] |
BM-MSCs and CB-MSCs | IFN-γ | In vivo model of GVHD | Reduction of the symptoms of GVHD | [66] |
UC-MSCs | IFN-γ; TNF-α | In vivo model of GVHD | Reduction of the clinical symptoms | [67] |
BM-MSCs | IL-6 | In vivo model of liver fibrosis | Reduction of liver injury | [68] |
UC-MSCs | IL-1β | In vivo model of sepsis | Increase in survival rate | [69] |
CB-MSCs | IFN-γ | In vivo model of acute kidney injury | Reduction of kidney injury | [70] |
AdMSCs | TNF-α | In vivo model of wound healing | Acceleration of wound closure and angiogenesis | [71] |
Priming with hypoxia | ||||
BM-MSCs | Hypoxia | In vivo model of traumatic brain injury | Improved neurogenesis and cognitive function | [47] |
AdMSCs | Hypoxia | In vivo model of hepatectomy | Enhanced liver regeneration | [48] |
UC-MSCs | Hypoxia | In vivo model of spinal cord injury | Improved axonal preservation | [52] |
AdMSCs | Hypoxia | In vivo model of hindlimb ischemia | Improvement of angiogenesis | [53] |
BM-MSCs | Hypoxia | In vivo model of hepatectomy | Enhanced liver regeneration | [54] |
BM-MSCs | Hypoxia | In vivo model of pulmonary fibrosis | Increased survival rate | [72] |
BM-MSCs | Hypoxia | In vivo model of hindlimb ischemia | Improvement of angiogenesis | [73] |
AdMSCs | Hypoxia | In vivo model of hindlimb ischemia | Improvement of functional recovery | [74] |
BM-MSCs | Hypoxia | In vivo model of radiation-induced lung injury | Improvement of antioxidant ability | [75] |
BM-MSCs | Hypoxia | In vivo model of lung IRI | Attenuation of lung injury | [76] |
AdMSCs | Hypoxia | In vivo model of acute kidney injury | Improvement of renal function | [77] |
AdMSCs | Hypoxia | In vivo model of acute kidney injury | Attenuation of kidney injury | [78] |
PMSCs | Hypoxia | In vivo model of scar formation | Reduction of scar formation | [79] |
AF-MSCs | Hypoxia | In vivo model of wound healing | Acceleration of wound healing | [80] |
BM-MSCs | Hypoxia | In vivo model of wound healing | Acceleration of wound healing | [81] |
BM-MSCs | Hypoxia | In vivo model of hindlimb ischemia | Improvement of muscle fiber regeneration | [82] |
DP-MSCs | Hypoxia | In vivo model of dental pulp injury | Regeneration of dental pulp | [83] |
BM-MSCs | Hypoxia | In vivo model of cerebral ischemia | Enhanced angiogenesis and neurogenesis | [84] |
BM-MSCs | Hypoxia | In vivo model of ischemic cortex | Reduction of infarct volume | [85] |
BM-MSCs | Hypoxia | In vivo model of myocardial infarction | Reduction of cardiac fibrosis | [86] |
BM-MSCs | Hypoxia | In vivo model of myocardial infarction | Improvement cardiac functions | [87] |
BM-MSCs | Hypoxia | In vivo model of myocardial infarction | Prevention of apoptosis in cardiomyocytes | [88] |
BM-MSCs | Hypoxia | In vivo model of myocardial infarction | Increased cardiomyocyte proliferation and function | [89] |
BM-MSCs | Hypoxia | In vivo model of myocardial infarction | Improved cardiac repair | [90] |
BM-MSCs | Hypoxia | In vivo IRI model of myocardium | Reduction of IRI | [91] |
Priming with 3D culture | ||||
BM-MSCs | 3D culture | In vivo model of peritonitis | Attenuation of inflammation | [92] |
UC-MSCs | 3D culture | In vivo model of arthritis | Attenuation of systemic arthritic manifestations | [93] |
CB-MSCs | 3D culture | In vivo model of hindlimb ischemia | Improvement of cell survival and angiogenesis | [94] |
AdMSCs | 3D culture | In vivo model of hindlimb ischemia | Improvement of angiogenesis | [95] |
AdMSCs | 3D culture | In vivo model of acute kidney injury | Amelioration of renal function | [96] |
AdMSCs | 3D culture | In vivo model of disc degeneration | Induction of disc repair | [97] |
BM-MSCs | 3D culture | In vivo model of bilateral calvarial defects | Induction of bone regeneration | [98] |
SMSCs | 3D cultures | In vivo model of osteochondral defects | Induction of cartilage regeneration | [99] |
BM-MSCs | 3D culture | In vivo model of myocardial infarction | Promotion of cardiac repair | [100] |
BM-MSCs | 3D cultures | In vivo model of myocardial infarction | Improvement of cardiac function | [101] |
- Citation: Miceli V. Use of priming strategies to advance the clinical application of mesenchymal stromal/stem cell-based therapy. World J Stem Cells 2024; 16(1): 7-18
- URL: https://www.wjgnet.com/1948-0210/full/v16/i1/7.htm
- DOI: https://dx.doi.org/10.4252/wjsc.v16.i1.7