<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Kang M</submitter><funding>NIDDK NIH HHS</funding><pagination>1226-35</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2848927</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>159(6)</volume><pubmed_abstract>&lt;h4>Background and purpose&lt;/h4>Excitation-transcriptional coupling involves communication between plasma membrane ion channels and gene expression in the nucleus. Calcium influx through L-type Ca(2+) channels induces phosphorylation of the transcription factor, cyclic-AMP response element binding protein (CREB) and downstream activation of the cyclic-AMP response element (CRE) promoter regions. Tyrosine nitration of Ca(2+) channels attenuates interactions with c-Src kinase, decreasing Ca(2+) channel currents and smooth muscle contraction during colonic inflammation. In this study we examined the effect of tyrosine nitration and colonic inflammation on Ca(2+) channel mediated phosphorylation of CREB and CRE activation.&lt;h4>Experimental approach&lt;/h4>CREB and phospho-CREB were detected by West</pubmed_abstract><journal>British journal of pharmacology</journal><pubmed_title>The effect of tyrosine nitration of L-type Ca2+ channels on excitation-transcription coupling in colonic inflammation.</pubmed_title><pmcid>PMC2848927</pmcid><funding_grant_id>R01 DK046367</funding_grant_id><funding_grant_id>DK046367</funding_grant_id><pubmed_authors>Kang M</pubmed_authors><pubmed_authors>Akbarali HI</pubmed_authors><pubmed_authors>Ross GR</pubmed_authors></additional><is_claimable>false</is_claimable><name>The effect of tyrosine nitration of L-type Ca2+ channels on excitation-transcription coupling in colonic inflammation.</name><description>&lt;h4>Background and purpose&lt;/h4>Excitation-transcriptional coupling involves communication between plasma membrane ion channels and gene expression in the nucleus. Calcium influx through L-type Ca(2+) channels induces phosphorylation of the transcription factor, cyclic-AMP response element binding protein (CREB) and downstream activation of the cyclic-AMP response element (CRE) promoter regions. Tyrosine nitration of Ca(2+) channels attenuates interactions with c-Src kinase, decreasing Ca(2+) channel currents and smooth muscle contraction during colonic inflammation. In this study we examined the effect of tyrosine nitration and colonic inflammation on Ca(2+) channel mediated phosphorylation of CREB and CRE activation.&lt;h4>Experimental approach&lt;/h4>CREB and phospho-CREB were detected by West</description><dates><release>2010-01-01T00:00:00Z</release><publication>2010 Mar</publication><modification>2025-06-01T00:53:52.622Z</modification><creation>2019-06-06T21:58:35Z</creation></dates><accession>S-EPMC2848927</accession><cross_references><pubmed>20128810</pubmed><doi>10.1111/j.1476-5381.2009.00599.x</doi></cross_references></HashMap>