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Integrin alpha-5 subunit is critical for the early stages of human pluripotent stem cell cardiac differentiation

The stem cell niche has a strong influence in the differentiation potential of human pluripotent stem cells with integrins playing a major role in communicating cells with the extracellular environment. However, it is not well understood how interactions between integrins and the extracellular matri...

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Detalles Bibliográficos
Autores principales: Neiman, Gabriel, Scarafía, María Agustina, La Greca, Alejandro, Santín Velazque, Natalia L., Garate, Ximena, Waisman, Ariel, Möbbs, Alan M., Kasai-Brunswick, Tais Hanae, Mesquita, Fernanda, Martire-Greco, Daiana, Moro, Lucía N., Luzzani, Carlos, Bastos Carvalho, Adriana, Sevlever, Gustavo E., Campos de Carvalho, Antonio, Guberman, Alejandra S., Miriuka, Santiago G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6889169/
https://www.ncbi.nlm.nih.gov/pubmed/31792288
http://dx.doi.org/10.1038/s41598-019-54352-2
Descripción
Sumario:The stem cell niche has a strong influence in the differentiation potential of human pluripotent stem cells with integrins playing a major role in communicating cells with the extracellular environment. However, it is not well understood how interactions between integrins and the extracellular matrix are involved in cardiac stem cell differentiation. To evaluate this, we performed a profile of integrins expression in two stages of cardiac differentiation: mesodermal progenitors and cardiomyocytes. We found an active regulation of the expression of different integrins during cardiac differentiation. In particular, integrin α5 subunit showed an increased expression in mesodermal progenitors, and a significant downregulation in cardiomyocytes. To analyze the effect of α5 subunit, we modified its expression by using a CRISPRi technique. After its downregulation, a significant impairment in the process of epithelial-to-mesenchymal transition was seen. Early mesoderm development was significantly affected due to a downregulation of key genes such as T Brachyury and TBX6. Furthermore, we observed that repression of integrin α5 during early stages led to a reduction in cardiomyocyte differentiation and impaired contractility. In summary, our results showed the link between changes in cell identity with the regulation of integrin α5 expression through the alteration of early stages of mesoderm commitment.