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Preclinical Studies and Clinical Prospects of Wharton’s Jelly-Derived MSC for Treatment of Acute Radiation Syndrome
PURPOSE OF REVIEW: Wharton’s jelly-derived mesenchymal stem cells (WJ-MSCs) have received widespread attention from researchers owing to the remarkable benefits offered by these cells over other stem cells. The primitive nature of WJ-MSCs, ease of isolation, differentiation ability, and immuno-modul...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer International Publishing
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8080090/ https://www.ncbi.nlm.nih.gov/pubmed/33936933 http://dx.doi.org/10.1007/s40778-021-00188-4 |
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author | Bandekar, Mayuri Maurya, Dharmendra K. Sharma, Deepak Sandur, Santosh K. |
author_facet | Bandekar, Mayuri Maurya, Dharmendra K. Sharma, Deepak Sandur, Santosh K. |
author_sort | Bandekar, Mayuri |
collection | PubMed |
description | PURPOSE OF REVIEW: Wharton’s jelly-derived mesenchymal stem cells (WJ-MSCs) have received widespread attention from researchers owing to the remarkable benefits offered by these cells over other stem cells. The primitive nature of WJ-MSCs, ease of isolation, differentiation ability, and immuno-modulatory nature make these cells superior to bone marrow MSCs and ideal to treat various human ailments. This review explores ability of WJ-MSCs to mitigate acute radiation syndrome caused by planned or unplanned radiation exposure. RECENT FINDINGS: Recent reports suggest that WJ-MSCs home to damaged tissues in irradiated host and mitigate radiation induced damage to radiosensitive tissues such as hematopoietic and gastrointestinal systems. WJ-MSCs and conditioned media were found to protect mice from radiation induced mortality and also prevent radiation dermatitis. Local irradiation-induced lung toxicity in mice was significantly reduced by CXCR4 over-expressing WJ-MSCs. SUMMARY: Emerging evidences support safety and effectiveness of WJ-MSCs for treatment of acute radiation syndrome and lung injury after planned or accidental exposure. Additionally, conditioned media collected after culturing WJ-MSCs can also be used for mitigation of radiation dermatitis. Clinical translation of these findings would be possible after careful evaluation of resilience, effectiveness, and molecular mechanism of action of xenogeneic WJ-MSCs in non-human primates. |
format | Online Article Text |
id | pubmed-8080090 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-80800902021-04-28 Preclinical Studies and Clinical Prospects of Wharton’s Jelly-Derived MSC for Treatment of Acute Radiation Syndrome Bandekar, Mayuri Maurya, Dharmendra K. Sharma, Deepak Sandur, Santosh K. Curr Stem Cell Rep Radiation Biology (C Porada and P Wilson, Section Editors) PURPOSE OF REVIEW: Wharton’s jelly-derived mesenchymal stem cells (WJ-MSCs) have received widespread attention from researchers owing to the remarkable benefits offered by these cells over other stem cells. The primitive nature of WJ-MSCs, ease of isolation, differentiation ability, and immuno-modulatory nature make these cells superior to bone marrow MSCs and ideal to treat various human ailments. This review explores ability of WJ-MSCs to mitigate acute radiation syndrome caused by planned or unplanned radiation exposure. RECENT FINDINGS: Recent reports suggest that WJ-MSCs home to damaged tissues in irradiated host and mitigate radiation induced damage to radiosensitive tissues such as hematopoietic and gastrointestinal systems. WJ-MSCs and conditioned media were found to protect mice from radiation induced mortality and also prevent radiation dermatitis. Local irradiation-induced lung toxicity in mice was significantly reduced by CXCR4 over-expressing WJ-MSCs. SUMMARY: Emerging evidences support safety and effectiveness of WJ-MSCs for treatment of acute radiation syndrome and lung injury after planned or accidental exposure. Additionally, conditioned media collected after culturing WJ-MSCs can also be used for mitigation of radiation dermatitis. Clinical translation of these findings would be possible after careful evaluation of resilience, effectiveness, and molecular mechanism of action of xenogeneic WJ-MSCs in non-human primates. Springer International Publishing 2021-04-28 2021 /pmc/articles/PMC8080090/ /pubmed/33936933 http://dx.doi.org/10.1007/s40778-021-00188-4 Text en © The Author(s), under exclusive licence to Springer Nature Switzerland AG 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Radiation Biology (C Porada and P Wilson, Section Editors) Bandekar, Mayuri Maurya, Dharmendra K. Sharma, Deepak Sandur, Santosh K. Preclinical Studies and Clinical Prospects of Wharton’s Jelly-Derived MSC for Treatment of Acute Radiation Syndrome |
title | Preclinical Studies and Clinical Prospects of Wharton’s Jelly-Derived MSC for Treatment of Acute Radiation Syndrome |
title_full | Preclinical Studies and Clinical Prospects of Wharton’s Jelly-Derived MSC for Treatment of Acute Radiation Syndrome |
title_fullStr | Preclinical Studies and Clinical Prospects of Wharton’s Jelly-Derived MSC for Treatment of Acute Radiation Syndrome |
title_full_unstemmed | Preclinical Studies and Clinical Prospects of Wharton’s Jelly-Derived MSC for Treatment of Acute Radiation Syndrome |
title_short | Preclinical Studies and Clinical Prospects of Wharton’s Jelly-Derived MSC for Treatment of Acute Radiation Syndrome |
title_sort | preclinical studies and clinical prospects of wharton’s jelly-derived msc for treatment of acute radiation syndrome |
topic | Radiation Biology (C Porada and P Wilson, Section Editors) |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8080090/ https://www.ncbi.nlm.nih.gov/pubmed/33936933 http://dx.doi.org/10.1007/s40778-021-00188-4 |
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