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Conversely, abnormal Ca<jats:sup>2+<\/jats:sup> signaling is often involved in the onset and progression of cardiovascular diseases, such as cardiac hypertrophy, heart failure, arteriosclerosis, and hypertension. In excitable cells, such as cardiac myocytes and vascular smooth muscle cells (VSMCs), membrane depolarization, and the subsequent elevation of cytosolic Ca<jats:sup>2+<\/jats:sup> concentration ([Ca<jats:sup>2+<\/jats:sup>]<jats:sub>cyt<\/jats:sub>) via voltage-dependent Ca<jats:sup>2+<\/jats:sup> channels (VDCCs) cause muscle contraction, which is known as excitation\u2013contraction coupling (E-C coupling). Elevated [Ca<jats:sup>2+<\/jats:sup>]<jats:sub>cyt<\/jats:sub> can also activate Ca<jats:sup>2+<\/jats:sup>-dependent enzymes, in some cases leading to changes in gene expression patterns and contributing to long-term cellular responses. This mechanism is referred to as excitation-transcription coupling (E-T coupling), and it is involved in both the adaptive and pathological responses of the cardiovascular system to chronic stimulation. Specific intracellular regions, known as Ca<jats:sup>2+<\/jats:sup> microdomains, exhibit localized increases in [Ca<jats:sup>2+<\/jats:sup>]<jats:sub>cyt<\/jats:sub>. Such localized Ca<jats:sup>2+<\/jats:sup> signaling is now known to be one of the molecular mechanisms controlling the diversity of Ca<jats:sup>2+<\/jats:sup> responses. These Ca<jats:sup>2+<\/jats:sup> microdomains are often formed by complexes consisting of Ca<jats:sup>2+<\/jats:sup> channels and downstream Ca<jats:sup>2+<\/jats:sup>-dependent enzymes localized by scaffolding proteins. This review outlines some of the molecular mechanisms and roles of Ca<jats:sup>2+<\/jats:sup> microdomain-based E-T coupling in cardiac myocytes and VSMCs. First, we discuss the major molecular components that are essential for functional Ca<jats:sup>2+<\/jats:sup> microdomains. For example, VDCC (Ca<jats:sub>V<\/jats:sub>1.2 channel), ryanodine receptor (RyR), Ca<jats:sup>2+<\/jats:sup>-dependent enzymes (Ca<jats:sup>2+<\/jats:sup>\/CaM-dependent kinase [CaMK], calcineurin [CaN], and calpain), and scaffolding proteins (A-kinase anchoring proteins [AKAPs], caveolin, and junctophilin). Next, we discuss the roles of Ca<jats:sup>2+<\/jats:sup> microdomain-based E-T coupling in physiological and pathophysiological remodeling in cardiac myocytes and vascular smooth muscle cells.<\/jats:p>","DOI":"10.1186\/s41232-025-00384-3","type":"journal-article","created":{"date-parts":[[2025,6,23]],"date-time":"2025-06-23T07:30:44Z","timestamp":1750663844000},"update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":6,"title":["Ca2+ microdomain-based excitation-transcription coupling in cardiac myocytes and vascular smooth muscle cells"],"prefix":"10.1186","volume":"45","author":[{"given":"Tsukasa","family":"Koide","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Wayne R.","family":"Giles","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Rubii","family":"Kondo","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yuji","family":"Imaizumi","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Hisao","family":"Yamamura","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-7879-6059","authenticated-orcid":false,"given":"Yoshiaki","family":"Suzuki","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"297","published-online":{"date-parts":[[2025,6,23]]},"reference":[{"key":"384_CR1","doi-asserted-by":"publisher","first-page":"517","DOI":"10.1038\/NRM1155","volume":"4","author":"MJ Berridge","year":"2003","unstructured":"Berridge MJ, Bootman MD, Roderick HL. 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