» Articles » PMID: 30603477

Mesenchymal Stem Cell-Based Therapies Against Podocyte Damage in Diabetic Nephropathy

Overview
Date 2019 Jan 4
PMID 30603477
Citations 17
Authors
Affiliations
Soon will be listed here.
Abstract

Injury to podocytes is an early event in diabetic nephropathy leading to proteinuria with possible progression to end-stage renal failure. The podocytes are unique and highly specialized cells that cover the outer layer of kidney ultra-filtration barrier and play an important role in glomerular function. In the past few decades, adult stem cells, such as mesenchymal stem cells (MSCs) with a regenerative and differentiative capacity have been extensively used in cell-based therapies. In addition to their capability for regeneration and differentiation, MSCs contributes to their by paracrine action of a series of growth factors antiapoptotic, mitogenic and other cytokine actions that actively participate in treatment of podocyte damage through prevention of podocyte effacement, detachment and apoptosis. It is hoped that novel stem cell-based therapies will be developed in the future to prevent podocyte injury, thereby reducing the burden of kidney disease.

Citing Articles

Effects of xenogeneic transplantation of umbilical cord-derived mesenchymal stem cells combined with irbesartan on renal podocyte damage in diabetic rats.

Meng J, Gao X, Liu X, Zheng W, Wang Y, Wang Y Stem Cell Res Ther. 2024; 15(1):239.

PMID: 39080783 PMC: 11289925. DOI: 10.1186/s13287-024-03844-8.


Unveiling diabetic nephropathy: a novel diagnostic model through single-cell sequencing and co-expression analysis.

Wang G, Zhao J, Zhou M, Lu H, Mao F Aging (Albany NY). 2024; 16(13):10972-10984.

PMID: 38968594 PMC: 11272118. DOI: 10.18632/aging.205982.


BM-MSCs alleviate diabetic nephropathy in male rats by regulating ER stress, oxidative stress, inflammation, and apoptotic pathways.

Khamis T, Abdelkhalek A, Abdellatif H, Dwidar N, Said A, Ahmed R Front Pharmacol. 2023; 14:1265230.

PMID: 38044936 PMC: 10690373. DOI: 10.3389/fphar.2023.1265230.


Synergism of calycosin and bone marrow-derived mesenchymal stem cells to combat podocyte apoptosis to alleviate adriamycin-induced focal segmental glomerulosclerosis.

Hu Q, Tan R, Zou Y, Li J, Fan J, Kantawong F World J Stem Cells. 2023; 15(6):617-631.

PMID: 37424951 PMC: 10324505. DOI: 10.4252/wjsc.v15.i6.617.


Bone marrow mesenchymal stem cell-derived exosomal miR-30e-5p ameliorates high-glucose induced renal proximal tubular cell pyroptosis by inhibiting ELAVL1.

Lv J, Hao Y, Wang X, Lu W, Xie L, Niu D Ren Fail. 2023; 45(1):2177082.

PMID: 36794663 PMC: 9937013. DOI: 10.1080/0886022X.2023.2177082.


References
1.
Morrison S, White P, Zock C, Anderson D . Prospective identification, isolation by flow cytometry, and in vivo self-renewal of multipotent mammalian neural crest stem cells. Cell. 1999; 96(5):737-49. DOI: 10.1016/s0092-8674(00)80583-8. View

2.
Inoki K, Haneda M, Maeda S, Koya D, Kikkawa R . TGF-beta 1 stimulates glucose uptake by enhancing GLUT1 expression in mesangial cells. Kidney Int. 1999; 55(5):1704-12. DOI: 10.1046/j.1523-1755.1999.00438.x. View

3.
Flyvbjerg A, Bennett W, Rasch R, Kopchick J, Scarlett J . Inhibitory effect of a growth hormone receptor antagonist (G120K-PEG) on renal enlargement, glomerular hypertrophy, and urinary albumin excretion in experimental diabetes in mice. Diabetes. 1999; 48(2):377-82. DOI: 10.2337/diabetes.48.2.377. View

4.
Terada Y, Inoshita S, Nakashima O, Tamamori M, Ito H, Kuwahara M . Cell cycle inhibitors (p27Kip1 and p21CIP1) cause hypertrophy in LLC-PK1 cells. Kidney Int. 1999; 56(2):494-501. DOI: 10.1046/j.1523-1755.1999.00568.x. View

5.
Meyer T, BENNETT P, Nelson R . Podocyte number predicts long-term urinary albumin excretion in Pima Indians with Type II diabetes and microalbuminuria. Diabetologia. 1999; 42(11):1341-4. DOI: 10.1007/s001250051447. View