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The potential role of integrin alpha 6 in human mesenchymal stem cells

Human mesenchymal stem cells (MSCs) are isolated from various adult and perinatal tissues. Although mesenchymal stem cells from multiple sources exhibit similar morphology and cell surface markers, they differ in their properties. In this study, we determined that the expression of integrin alpha 6...

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Autores principales: Al-Obaide, Mohammed, Ishmakej, Albi, Brown, Christina, Mazzella, Matteo, Agosta, Patrina, Perez-Cruet, Mick, Chaudhry, G. Rasul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9535380/
https://www.ncbi.nlm.nih.gov/pubmed/36212156
http://dx.doi.org/10.3389/fgene.2022.968228
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author Al-Obaide, Mohammed
Ishmakej, Albi
Brown, Christina
Mazzella, Matteo
Agosta, Patrina
Perez-Cruet, Mick
Chaudhry, G. Rasul
author_facet Al-Obaide, Mohammed
Ishmakej, Albi
Brown, Christina
Mazzella, Matteo
Agosta, Patrina
Perez-Cruet, Mick
Chaudhry, G. Rasul
author_sort Al-Obaide, Mohammed
collection PubMed
description Human mesenchymal stem cells (MSCs) are isolated from various adult and perinatal tissues. Although mesenchymal stem cells from multiple sources exhibit similar morphology and cell surface markers, they differ in their properties. In this study, we determined that the expression of integrin alpha 6 (ITGA6) and ITGA6 antisense RNA (ITGA6-AS1) correlates with the proliferation, cell size, and differentiation potential. The expression of ITGA6 was inversely correlated with ITGA6-AS1 in MSCs. The expression of ITGA6 was higher, but ITGA6-AS1 was lower in MSCs from cord placenta junction, cord tissue, and Wharton’s jelly. In contrast, ITGA6 expression was lower, while ITGA6-AS1 was higher in MSCs from the placenta. The bioinformatic analysis showed that ITGA6 genomic DNA transcribes ITGA6-AS1 from the reverse strand, overlapping ITGA6 exon-2. Additionally, we identify several putative promoters (P1-P10) of ITGA6. ITGA6-P10 is CG rich and contains CGI. EMBOSS Cpgplot software revealed a CGI length of 180 bp that extends from nucleotide 125 to 304 of the P10 sequence. We suggest that the post-transcriptional regulation of the ITGA6 in mesenchymal stem cells is controlled by the ITGA6-AS1, which could be a critical factor responsible for the heterogeneity in function and cell fate of human MSCs. These results may provide further impetus for investigations to unravel the mechanisms of ITGA6 regulation that could help maintain or improve the properties of mesenchymal stem cells.
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spelling pubmed-95353802022-10-07 The potential role of integrin alpha 6 in human mesenchymal stem cells Al-Obaide, Mohammed Ishmakej, Albi Brown, Christina Mazzella, Matteo Agosta, Patrina Perez-Cruet, Mick Chaudhry, G. Rasul Front Genet Genetics Human mesenchymal stem cells (MSCs) are isolated from various adult and perinatal tissues. Although mesenchymal stem cells from multiple sources exhibit similar morphology and cell surface markers, they differ in their properties. In this study, we determined that the expression of integrin alpha 6 (ITGA6) and ITGA6 antisense RNA (ITGA6-AS1) correlates with the proliferation, cell size, and differentiation potential. The expression of ITGA6 was inversely correlated with ITGA6-AS1 in MSCs. The expression of ITGA6 was higher, but ITGA6-AS1 was lower in MSCs from cord placenta junction, cord tissue, and Wharton’s jelly. In contrast, ITGA6 expression was lower, while ITGA6-AS1 was higher in MSCs from the placenta. The bioinformatic analysis showed that ITGA6 genomic DNA transcribes ITGA6-AS1 from the reverse strand, overlapping ITGA6 exon-2. Additionally, we identify several putative promoters (P1-P10) of ITGA6. ITGA6-P10 is CG rich and contains CGI. EMBOSS Cpgplot software revealed a CGI length of 180 bp that extends from nucleotide 125 to 304 of the P10 sequence. We suggest that the post-transcriptional regulation of the ITGA6 in mesenchymal stem cells is controlled by the ITGA6-AS1, which could be a critical factor responsible for the heterogeneity in function and cell fate of human MSCs. These results may provide further impetus for investigations to unravel the mechanisms of ITGA6 regulation that could help maintain or improve the properties of mesenchymal stem cells. Frontiers Media S.A. 2022-09-16 /pmc/articles/PMC9535380/ /pubmed/36212156 http://dx.doi.org/10.3389/fgene.2022.968228 Text en Copyright © 2022 Al-Obaide, Ishmakej, Brown, Mazzella, Agosta, Perez-Cruet and Chaudhry. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Al-Obaide, Mohammed
Ishmakej, Albi
Brown, Christina
Mazzella, Matteo
Agosta, Patrina
Perez-Cruet, Mick
Chaudhry, G. Rasul
The potential role of integrin alpha 6 in human mesenchymal stem cells
title The potential role of integrin alpha 6 in human mesenchymal stem cells
title_full The potential role of integrin alpha 6 in human mesenchymal stem cells
title_fullStr The potential role of integrin alpha 6 in human mesenchymal stem cells
title_full_unstemmed The potential role of integrin alpha 6 in human mesenchymal stem cells
title_short The potential role of integrin alpha 6 in human mesenchymal stem cells
title_sort potential role of integrin alpha 6 in human mesenchymal stem cells
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9535380/
https://www.ncbi.nlm.nih.gov/pubmed/36212156
http://dx.doi.org/10.3389/fgene.2022.968228
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