Elevated glucose alters global gene expression and tenascin-C alternative splicing in mesangial cells
Matrix Biology Plus, ISSN: 2590-0285, Vol: 8, Page: 100048
2020
- 7Citations
- 12Captures
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Metrics Details
- Citations7
- Citation Indexes7
- Captures12
- Readers12
- 12
Article Description
Mesangial cells are the major extracellular matrix (ECM)-producing cells in the kidney glomerulus and, when exposed to elevated glucose levels, they up-regulate assembly of fibronectin (FN) and other ECM proteins. Increases in glucose concentration are known to alter gene expression; here we investigated the connection between increased ECM production and changes in gene expression in mesangial cells. Comparison of mesangial cells grown in normal or high glucose conditions by RNA-sequencing showed significant expression changes in over 6000 genes and, when grouped by KEGG pathway analysis, identified the ECM-receptor interaction and focal adhesion pathways among the top 5 upregulated pathways. Of note was the significant increase in expression of tenascin-C (TN-C), a known regulator of FN matrix assembly. Mouse TN-C has multiple isoforms due to alternative splicing of 6 FNIII repeat exons. In addition to the transcriptional increase with high glucose, exon inclusion via alternative splicing was also changed resulting in production of higher molecular weight isoforms of TN-C. Mesangial cells grown in normal glucose secreted small isoforms with 1–2 variable repeats included whereas in high glucose large isoforms estimated to include 5 repeats were secreted. Unlike the smaller isoforms, the larger TN-C was not detected in the FN matrix. This change in TN-C isoforms may affect the regulation of FN matrix assembly and in this way may contribute to increased ECM accumulation under high glucose conditions.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S2590028520300296; http://dx.doi.org/10.1016/j.mbplus.2020.100048; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85094587960&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/33543041; https://linkinghub.elsevier.com/retrieve/pii/S2590028520300296; https://dx.doi.org/10.1016/j.mbplus.2020.100048
Elsevier BV
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