Abstract
Kidney Disease (KD), has a high global prevalence and accounts for one of the most prominent causes of morbidity and mortality in the twenty-first century. Despite the advances in our understanding of its pathophysiology, the only available therapy options are dialysis and kidney transplantation. Mesenchymal stem cells (MSCs) have proven to be a viable choice for KD therapy due to their antiapoptotic, immunomodulatory, antioxidative, and pro-angiogenic activities. However, the low engraftment, low survival rate, diminished paracrine ability, and delayed delivery of MSCs are the major causes of the low clinical efficacy. A number of preconditioning regimens are being tested to increase the therapeutic capabilities of MSCs. In this review, we highlight the various strategies to prime MSCs and their protective effects in kidney diseases.
Graphical Abstract
Preconditioning Strategies of Mesenchymal Stem cell in Kidney Disease
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Data Availability
No new data were generated or analyzed in support of this research.
Abbreviations
- KD:
-
Kidney disease
- AKI:
-
Acute Kidney Disease
- CKD:
-
Chronic Kidney Disease
- CsA:
-
Cyclosporine A
- CA:
-
Calycosin
- DPO:
-
Darbepoetin-α
- DKD:
-
Diabetic kidney disease
- DM:
-
Diabetes mellitus
- DN:
-
Diabetic nephropathy
- ESRD:
-
End Stage Renal Disease
- EPO:
-
Erythropoietin
- EpoR:
-
EPO receptor
- EPCs:
-
Endothelial progenitor cells
- FGF:
-
Fibroblast Growth Factor
- FOXO3:
-
Forkhead box O3
- GFR:
-
Glomerular Filtration Rate
- HGF:
-
Hepatocyte Growth Factor
- HSC:
-
Hematopoietic stem cells
- HE:
-
Haematoxylin and eosin
- HIF:
-
Hypoxia-inducible factor
- IGF-1:
-
Insulin like growth factor-1
- IRI:
-
Ischemia/reperfusion induced
- EVs:
-
Extracellular vesicles
- BM-MSCs:
-
Bone Marrow derived MSCs
- MSC:
-
Mesenchymal Stem Cell
- MV:
-
Microvesicles
- SOD-1:
-
Superoxide dismutase 1
- HO-1:
-
Heme oxygenase 1
- KHS:
-
Kidney homogenate supernatant
- MSCs:
-
Mesenchymal stem cells;
- A-ADMSCs:
-
Apoptotic adipose-derived MSCs
- bFGF:
-
Basic fibroblast growth factor
- UUO:
-
Unilateral ureteral obstruction
- hBM-MSCs:
-
Human bone marrow mesenchymal stem cells
- SOD-1:
-
Superoxide dismutase 1
- CPT1A:
-
Carnitine palmitoyl-transferase 1A
- ECM:
-
Extracellular matrix
- MMP12:
-
Matrix metalloproteinase 12
- UUO:
-
Unilateral ureteric obstruction
- SIRT1:
-
Silent information regulator 1
- TNF- α:
-
Tumour Necrosis Factor- alpha
- VEGF:
-
Vascular Endothelial Growth Factor
- IGF-1C:
-
C domain of insulin-like growth factor-1
- AKC:
-
Artificial kidney capsule
- ECM:
-
Extracellular matrix (ECM)
- hP-MSCs:
-
Human placenta-derived mesenchymal stem cells
- TGF‐β:
-
Transforming growth factor‐β
- RTECs':
-
Renal Tubular Epithelial Cells
- ROS:
-
Reactive Oxygen Species
- PDGF:
-
Platelet Derived Growth Factor
- Fmoc-FFSNAP:
-
Fmoc-diphenylalanine S-nitroso-N-acetyl penicillamine hydrogel
- ADSCs:
-
Adipose Derived Stem Cell
- UC MSCs:
-
Umbilical derived Mesenchymal Stem Cells
- CPT1A:
-
Carnitine palmitoyl-transferase 1A
- α‐SMA:
-
α-Smooth muscle actin
- eGFR:
-
Estimated glomerular filtration rate
- EMCH:
-
Extracellular matrix hydrogel
- CLP:
-
Caecal ligation and puncture
- WJ-MSCs :
-
Wharton Jelly Derived Mesenchymal Stem Cells
- hAD-MSCs:
-
Human Adipose Derived Mesenchymal Stem Cell
- hMSCs:
-
Human Mesenchymal Stem Cells
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Makkar, D., Gakhar, D., Mishra, V. et al. Fine Tuning Mesenchymal Stromal Cells – Code For Mitigating Kidney Diseases. Stem Cell Rev and Rep 20, 738–754 (2024). https://doi.org/10.1007/s12015-024-10684-9
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DOI: https://doi.org/10.1007/s12015-024-10684-9