Related Experiment Video
Updated: Sep 21, 2025

Purification and Transplantation of Myogenic Progenitor Cell Derived Exosomes to Improve Cardiac Function in Duchenne Muscular Dystrophic Mice
Published on: April 10, 2019
Exosomes Derived from BM-MSCs Mitigate the Development of Chronic Kidney Damage Post-Menopause via Interfering with
Wardah A Alasmari1, Ahmed Abdelfattah-Hassan2,3, Hanaa M El-Ghazali2
1Department of Anatomy, Faculty of Medicine, Umm Al-Qura University, Makkah 24230, Saudi Arabia.
Abstract:
The rate of chronic kidney disease (CKD) is increasing globally, and it is caused by continuous damage to kidney tissue. With time the renal damage becomes irreversible, leading to CKD development. In females, post-menopause lack of estrogen supply has been described as a risk factor for CKD development, and studies targeting post-menopause CKD are scarce. In the present study, we used exosomes isolated from bone marrow mesenchymal stem/stromal cells (BM-MSCs) to test their therapeutic potential against the development of CKD. At first, the menopause model was achieved by surgical bilateral ovariectomy in female albino rats. After that, 100 µg of exosomes was given to ovariectomized rats, and the study continued for 2 months. Changes in urine volume, urine protein content, kidney function biochemical parameters (creatinine and BUN), kidney antioxidant parameters (SOD, GPx and CAT), histological changes, immunohistochemical levels of caspase 3, and the gene expression of NGAL (related to kidney damage), TGFβ1 and αSMA (related to fibrosis and EMT), and caspase 3 (related to apoptosis) were studied. After the ovariectomy, the occurrence of CKD was confirmed in the rats by the drastic reduction of serum estrogen and progesterone levels, reduced urine output, increased urinary protein excretion, elevated serum creatinine and BUN, reduced GPx SOD, and CAT in kidney tissue, degenerative and fibrotic lesions in the histopathological examination, higher immunohistochemical expression of caspase 3 and increased expression of all studied genes. After exosomes administration, the entire chronic inflammatory picture in the kidney was corrected, and a near-normal kidney structure and function were attained. This study shows for the first time that BM-MSCs exosomes are potent for reducing apoptosis and fibrosis levels and, thus, can reduce the chronic damage of the kidneys in females that are in their menopause period. Therefore, MSCs-derived exosomes should be considered a valuable therapy for preserving postmenopausal kidney structure and function and, subsequently, could improve the quality of females' life during menopause.
Insights
Bone marrow mesenchymal stem cell exosomes show promise in treating chronic kidney disease (CKD) in postmenopausal rats. This therapy helps reduce kidney damage, apoptosis, and fibrosis, potentially improving women's health during menopause.
Area of Science:
- Nephrology
- Regenerative Medicine
- Biotechnology
Background:
- Chronic kidney disease (CKD) is a growing global health concern, often resulting from irreversible kidney damage.
- Estrogen deficiency post-menopause is a recognized risk factor for CKD in women, yet research in this area is limited.
Purpose of the Study:
- To investigate the therapeutic potential of exosomes derived from bone marrow mesenchymal stem/stromal cells (BM-MSCs) in preventing CKD development in a postmenopausal rat model.
Main Methods:
- A surgical bilateral ovariectomy was performed on female rats to induce a menopausal state.
- Ovariectomized rats received 100 µg of BM-MSCs exosomes for 2 months.
- Evaluated parameters included urine output, protein content, kidney function markers (creatinine, BUN), antioxidant status (SOD, GPx, CAT), histological changes, caspase 3 expression, and gene expression related to kidney damage, fibrosis, and apoptosis.
Main Results:
- Ovariectomy induced CKD markers: reduced estrogen/progesterone, decreased urine output, increased proteinuria, elevated creatinine/BUN, diminished antioxidant enzymes, and histological damage.
- Exosome administration corrected the inflammatory kidney profile, restoring near-normal kidney structure and function.
- BM-MSCs exosomes significantly reduced apoptosis and fibrosis markers.
Conclusions:
- BM-MSCs exosomes demonstrate significant therapeutic potential for mitigating kidney damage in postmenopausal females.
- This therapy effectively reduces apoptosis and fibrosis, preserving kidney structure and function.
- MSCs-derived exosomes represent a promising therapeutic strategy to enhance the quality of life for postmenopausal women by protecting kidney health.
More Related Videos
Related Concept Videos
Mesenchymal Stem Cells
Overview of Exosomes
Stahl et al. discovered exosomes in 1983, but the exosomes were initially considered waste products released from the...

