文章基本信息

标题：NG2/CSPG4, CD146/MCAM and VAP1/AOC3 are regulated by myocardin-related transcription factors in smooth muscle cells
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作者：Catarina Rippe ; Björn Morén ; Li Liu 等
期刊名称：Scientific Reports
电子版ISSN：2045-2322
出版年度：2021
卷号：11
期号：1
页码：5955
DOI：10.1038/s41598-021-85335-x
出版社：Springer Nature
摘要：Abstract The present work addressed the hypothesis that NG2/ CSPG4 , CD146/ MCAM , and VAP1/ AOC3 are target genes of myocardin-related transcription factors (MRTFs: myocardin/ MYOCD , MRTF-A/ MKL1 , MRTF-B/ MKL2 ) and serum response factor ( SRF ). Using a bioinformatics approach, we found that CSPG4 , MCAM , and AOC3 correlate with MYOCD , MRTF-A/ MKL1 , and SRF across human tissues. No other transcription factor correlated as strongly with these transcripts as SRF . Overexpression of MRTFs increased both mRNA and protein levels of CSPG4 , MCAM , and AOC3 in cultured human smooth muscle cells (SMCs). Imaging confirmed increased staining for CSPG4, MCAM, and AOC3 in MRTF-A/ MKL1 -transduced cells. MRTFs exert their effects through SRF, and the MCAM and AOC3 gene loci contained binding sites for SRF. SRF silencing reduced the transcript levels of these genes, and time-courses of induction paralleled the direct target ACTA2 . MRTF-A/ MKL1 increased the activity of promoter reporters for MCAM and AOC3 , and transcriptional activation further depended on the chromatin remodeling enzyme KDM3A. CSPG4 , MCAM , and AOC3 responded to the MRTF-SRF inhibitor CCG-1423, to actin dynamics, and to ternary complex factors. Coincidental detection of these proteins should reflect MRTF-SRF activity, and beyond SMCs, we observed co-expression of CD146/ MCAM , NG2/ CSPG4 , and VAP1/ AOC3 in pericytes and endothelial cells in the human brain. This work identifies highly responsive vascular target genes of MRTF-SRF signaling that are regulated via a mechanism involving KDM3A.
其他摘要：Abstract The present work addressed the hypothesis that NG2/ CSPG4 , CD146/ MCAM , and VAP1/ AOC3 are target genes of myocardin-related transcription factors (MRTFs: myocardin/ MYOCD , MRTF-A/ MKL1 , MRTF-B/ MKL2 ) and serum response factor ( SRF ). Using a bioinformatics approach, we found that CSPG4 , MCAM , and AOC3 correlate with MYOCD , MRTF-A/ MKL1 , and SRF across human tissues. No other transcription factor correlated as strongly with these transcripts as SRF . Overexpression of MRTFs increased both mRNA and protein levels of CSPG4 , MCAM , and AOC3 in cultured human smooth muscle cells (SMCs). Imaging confirmed increased staining for CSPG4, MCAM, and AOC3 in MRTF-A/ MKL1 -transduced cells. MRTFs exert their effects through SRF, and the MCAM and AOC3 gene loci contained binding sites for SRF. SRF silencing reduced the transcript levels of these genes, and time-courses of induction paralleled the direct target ACTA2 . MRTF-A/ MKL1 increased the activity of promoter reporters for MCAM and AOC3 , and transcriptional activation further depended on the chromatin remodeling enzyme KDM3A. CSPG4 , MCAM , and AOC3 responded to the MRTF-SRF inhibitor CCG-1423, to actin dynamics, and to ternary complex factors. Coincidental detection of these proteins should reflect MRTF-SRF activity, and beyond SMCs, we observed co-expression of CD146/ MCAM , NG2/ CSPG4 , and VAP1/ AOC3 in pericytes and endothelial cells in the human brain. This work identifies highly responsive vascular target genes of MRTF-SRF signaling that are regulated via a mechanism involving KDM3A.