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                <identifier>oai:data.mendeley.com/ngktxkzhw7.1</identifier>
                <datestamp>2024-12-11T17:09:28Z</datestamp>
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    <dc:creator>pandey, sarita</dc:creator>
    <dc:title>     Pax6 co-expresses and gets compartmentalized in the heart of diabetic mice                                     </dc:title>
    <dc:publisher>Mendeley Data</dc:publisher>
    <dc:description>The Paired box (Pax6), a highly conserved transcription factor, and Tgf-β1 are involved in various cellular functions such as differentiation, activation of extracellular matrix proteins, epithelial-mesenchymal transition, production of cytokines, MAPK, NF-kB, PI3K, Tgf-βs, TLRs, and insulin signaling pathways.  In the present study, it was observed that the epicardial, myocardial, and endocardial structures were distorted, and co-expression and compartmentalization of Pax6 and Tgf-β1 occurred in different layers of diabetic mice compared to the control. In the heart, Pax6 expression promotes cardiac fibroblast differentiation via maintaining Tgf-β1 levels. The Tgf-β1 is a pleiotropic cytokine involved in many biological functions. The ligand of Tgf-β1 and their signaling molecules are necessary for the heart&apos;s development and normal cardiovascular function. The high level of glucose stimulates Tgf-β1 dependent pathways and activates Tgf-β1 further leading to cardiac fibrosis which includes cardiac hypertrophy through SMAD-dependent and independent (canonical and non-canonical) pathways. Since expression of Tgf-β1 and Pax6 has been proven to be critical for the functional anatomy of the heart, Tgf-β1 and Pax6 might function like tissue-dependent regulation through various signaling pathways or networks. Results suggest that Tgf-β1 and Pax6 have a crucial role in the differentiation and development of cardiac fibroblasts and also regulate the differentiation of fibroblasts into myofibroblasts via SMAD-dependent and independent (canonical and non-canonical) pathways. However, the maintenance and differentiation of cardiac fibroblasts may lead to novel therapy in some patients with cardiac dysfunction. </dc:description>
    <dc:subject>Western Blot</dc:subject>
    <dc:subject>Immunochemistry</dc:subject>
    <dc:subject>Animal Histology</dc:subject>
    <dc:subject>Quantitative Reverse Transcription Polymerase Chain Reaction</dc:subject>
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    <dc:identifier>doi:10.17632/ngktxkzhw7.1</dc:identifier>
    <dc:identifier>oai:data.mendeley.com/ngktxkzhw7.1</dc:identifier>
    <dc:rights>Creative Commons Attribution 4.0 International</dc:rights>
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    <dc:date>2024-12-11T17:09:28Z</dc:date>
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