Loading…
Mitochondria-associated endoplasmic reticulum membranes as a therapeutic target for cardiovascular diseases
Cardiovascular diseases (CVDs) are currently the leading cause of death worldwide. In 2022, the CVDs contributed to 19.8 million deaths globally, accounting for one-third of all global deaths. With an aging population and changing lifestyles, CVDs pose a major threat to human health. Mitochondria-as...
Saved in:
Published in: | Frontiers in pharmacology 2024-04, Vol.15, p.1398381 |
---|---|
Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | cdi_FETCH-LOGICAL-c420t-39dc33702304e0b9718cfcdb08954160642924d731e5a6308734396990d7a7423 |
container_end_page | |
container_issue | |
container_start_page | 1398381 |
container_title | Frontiers in pharmacology |
container_volume | 15 |
creator | Ding, Yanqiu Liu, Nanyang Zhang, Dawu Guo, Lijun Shang, Qinghua Liu, Yicheng Ren, Gaocan Ma, Xiaochang |
description | Cardiovascular diseases (CVDs) are currently the leading cause of death worldwide. In 2022, the CVDs contributed to 19.8 million deaths globally, accounting for one-third of all global deaths. With an aging population and changing lifestyles, CVDs pose a major threat to human health. Mitochondria-associated endoplasmic reticulum membranes (MAMs) are communication platforms between cellular organelles and regulate cellular physiological functions, including apoptosis, autophagy, and programmed necrosis. Further research has shown that MAMs play a critical role in the pathogenesis of CVDs, including myocardial ischemia and reperfusion injury, heart failure, pulmonary hypertension, and coronary atherosclerosis. This suggests that MAMs could be an important therapeutic target for managing CVDs. The goal of this study is to summarize the protein complex of MAMs, discuss its role in the pathological mechanisms of CVDs in terms of its functions such as Ca
transport, apoptotic signaling, and lipid metabolism, and suggest the possibility of MAMs as a potential therapeutic approach. |
doi_str_mv | 10.3389/fphar.2024.1398381 |
format | article |
fullrecord | <record><control><sourceid>proquest_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_11ce101561c04be3a1520f177ed3ff19</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_11ce101561c04be3a1520f177ed3ff19</doaj_id><sourcerecordid>3050174819</sourcerecordid><originalsourceid>FETCH-LOGICAL-c420t-39dc33702304e0b9718cfcdb08954160642924d731e5a6308734396990d7a7423</originalsourceid><addsrcrecordid>eNpVkUtv3SAQha2qVROl-QNdVF5241tgMJhVVUV9RErVTbtGYxjfS2pfXLAj9d-X-2iUICRGDOebI05VveVsA9CZD8O8w7QRTMgNB9NBx19Ul1wpaEzHxcsn9UV1nfM9KwuMASVfVxfQKSONkJfV7-9hiW4X9z4FbDDn6AIu5Gva-ziPmKfg6kRLcOu4TvVEU59wT7nGsutlRwlnWku7XjBtaamHmGqHyYf4gLmIMNU-ZMJM-U31asAx0_X5vKp-ffn88-Zbc_fj6-3Np7vGScGWBox3AJoJYJJYbzTv3OB8zzrTSq6YkqJY9xo4taiAdRokGGUM8xq1FHBV3Z64PuK9nVOYMP21EYM9XsS0tZiK5ZEs5444463ijsmeAHkr2MC1Jg_DwE1hfTyx5rWfyDvaLwnHZ9DnnX3Y2W18KGSmuNQHN-_PhBT_rJQXO4XsaBzLN8Y1W2At41p2x2Hi9NSlmHOi4XEOZ_aQuj2mbg-p23PqRfTuqcNHyf-M4R_OyqqC</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3050174819</pqid></control><display><type>article</type><title>Mitochondria-associated endoplasmic reticulum membranes as a therapeutic target for cardiovascular diseases</title><source>PubMed Central</source><creator>Ding, Yanqiu ; Liu, Nanyang ; Zhang, Dawu ; Guo, Lijun ; Shang, Qinghua ; Liu, Yicheng ; Ren, Gaocan ; Ma, Xiaochang</creator><creatorcontrib>Ding, Yanqiu ; Liu, Nanyang ; Zhang, Dawu ; Guo, Lijun ; Shang, Qinghua ; Liu, Yicheng ; Ren, Gaocan ; Ma, Xiaochang</creatorcontrib><description>Cardiovascular diseases (CVDs) are currently the leading cause of death worldwide. In 2022, the CVDs contributed to 19.8 million deaths globally, accounting for one-third of all global deaths. With an aging population and changing lifestyles, CVDs pose a major threat to human health. Mitochondria-associated endoplasmic reticulum membranes (MAMs) are communication platforms between cellular organelles and regulate cellular physiological functions, including apoptosis, autophagy, and programmed necrosis. Further research has shown that MAMs play a critical role in the pathogenesis of CVDs, including myocardial ischemia and reperfusion injury, heart failure, pulmonary hypertension, and coronary atherosclerosis. This suggests that MAMs could be an important therapeutic target for managing CVDs. The goal of this study is to summarize the protein complex of MAMs, discuss its role in the pathological mechanisms of CVDs in terms of its functions such as Ca
transport, apoptotic signaling, and lipid metabolism, and suggest the possibility of MAMs as a potential therapeutic approach.</description><identifier>ISSN: 1663-9812</identifier><identifier>EISSN: 1663-9812</identifier><identifier>DOI: 10.3389/fphar.2024.1398381</identifier><identifier>PMID: 38694924</identifier><language>eng</language><publisher>Switzerland: Frontiers Media S.A</publisher><subject>cardiovascular diseases ; coronary atherosclerosis ; mitochondria-associated endoplasmic reticulum membrane ; myocardial ischemia ; Pharmacology ; therapeutic target</subject><ispartof>Frontiers in pharmacology, 2024-04, Vol.15, p.1398381</ispartof><rights>Copyright © 2024 Ding, Liu, Zhang, Guo, Shang, Liu, Ren and Ma.</rights><rights>Copyright © 2024 Ding, Liu, Zhang, Guo, Shang, Liu, Ren and Ma. 2024 Ding, Liu, Zhang, Guo, Shang, Liu, Ren and Ma</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c420t-39dc33702304e0b9718cfcdb08954160642924d731e5a6308734396990d7a7423</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11061472/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11061472/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,724,777,781,882,27905,27906,53772,53774</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38694924$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ding, Yanqiu</creatorcontrib><creatorcontrib>Liu, Nanyang</creatorcontrib><creatorcontrib>Zhang, Dawu</creatorcontrib><creatorcontrib>Guo, Lijun</creatorcontrib><creatorcontrib>Shang, Qinghua</creatorcontrib><creatorcontrib>Liu, Yicheng</creatorcontrib><creatorcontrib>Ren, Gaocan</creatorcontrib><creatorcontrib>Ma, Xiaochang</creatorcontrib><title>Mitochondria-associated endoplasmic reticulum membranes as a therapeutic target for cardiovascular diseases</title><title>Frontiers in pharmacology</title><addtitle>Front Pharmacol</addtitle><description>Cardiovascular diseases (CVDs) are currently the leading cause of death worldwide. In 2022, the CVDs contributed to 19.8 million deaths globally, accounting for one-third of all global deaths. With an aging population and changing lifestyles, CVDs pose a major threat to human health. Mitochondria-associated endoplasmic reticulum membranes (MAMs) are communication platforms between cellular organelles and regulate cellular physiological functions, including apoptosis, autophagy, and programmed necrosis. Further research has shown that MAMs play a critical role in the pathogenesis of CVDs, including myocardial ischemia and reperfusion injury, heart failure, pulmonary hypertension, and coronary atherosclerosis. This suggests that MAMs could be an important therapeutic target for managing CVDs. The goal of this study is to summarize the protein complex of MAMs, discuss its role in the pathological mechanisms of CVDs in terms of its functions such as Ca
transport, apoptotic signaling, and lipid metabolism, and suggest the possibility of MAMs as a potential therapeutic approach.</description><subject>cardiovascular diseases</subject><subject>coronary atherosclerosis</subject><subject>mitochondria-associated endoplasmic reticulum membrane</subject><subject>myocardial ischemia</subject><subject>Pharmacology</subject><subject>therapeutic target</subject><issn>1663-9812</issn><issn>1663-9812</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNpVkUtv3SAQha2qVROl-QNdVF5241tgMJhVVUV9RErVTbtGYxjfS2pfXLAj9d-X-2iUICRGDOebI05VveVsA9CZD8O8w7QRTMgNB9NBx19Ul1wpaEzHxcsn9UV1nfM9KwuMASVfVxfQKSONkJfV7-9hiW4X9z4FbDDn6AIu5Gva-ziPmKfg6kRLcOu4TvVEU59wT7nGsutlRwlnWku7XjBtaamHmGqHyYf4gLmIMNU-ZMJM-U31asAx0_X5vKp-ffn88-Zbc_fj6-3Np7vGScGWBox3AJoJYJJYbzTv3OB8zzrTSq6YkqJY9xo4taiAdRokGGUM8xq1FHBV3Z64PuK9nVOYMP21EYM9XsS0tZiK5ZEs5444463ijsmeAHkr2MC1Jg_DwE1hfTyx5rWfyDvaLwnHZ9DnnX3Y2W18KGSmuNQHN-_PhBT_rJQXO4XsaBzLN8Y1W2At41p2x2Hi9NSlmHOi4XEOZ_aQuj2mbg-p23PqRfTuqcNHyf-M4R_OyqqC</recordid><startdate>20240417</startdate><enddate>20240417</enddate><creator>Ding, Yanqiu</creator><creator>Liu, Nanyang</creator><creator>Zhang, Dawu</creator><creator>Guo, Lijun</creator><creator>Shang, Qinghua</creator><creator>Liu, Yicheng</creator><creator>Ren, Gaocan</creator><creator>Ma, Xiaochang</creator><general>Frontiers Media S.A</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20240417</creationdate><title>Mitochondria-associated endoplasmic reticulum membranes as a therapeutic target for cardiovascular diseases</title><author>Ding, Yanqiu ; Liu, Nanyang ; Zhang, Dawu ; Guo, Lijun ; Shang, Qinghua ; Liu, Yicheng ; Ren, Gaocan ; Ma, Xiaochang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c420t-39dc33702304e0b9718cfcdb08954160642924d731e5a6308734396990d7a7423</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>cardiovascular diseases</topic><topic>coronary atherosclerosis</topic><topic>mitochondria-associated endoplasmic reticulum membrane</topic><topic>myocardial ischemia</topic><topic>Pharmacology</topic><topic>therapeutic target</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ding, Yanqiu</creatorcontrib><creatorcontrib>Liu, Nanyang</creatorcontrib><creatorcontrib>Zhang, Dawu</creatorcontrib><creatorcontrib>Guo, Lijun</creatorcontrib><creatorcontrib>Shang, Qinghua</creatorcontrib><creatorcontrib>Liu, Yicheng</creatorcontrib><creatorcontrib>Ren, Gaocan</creatorcontrib><creatorcontrib>Ma, Xiaochang</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Frontiers in pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ding, Yanqiu</au><au>Liu, Nanyang</au><au>Zhang, Dawu</au><au>Guo, Lijun</au><au>Shang, Qinghua</au><au>Liu, Yicheng</au><au>Ren, Gaocan</au><au>Ma, Xiaochang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mitochondria-associated endoplasmic reticulum membranes as a therapeutic target for cardiovascular diseases</atitle><jtitle>Frontiers in pharmacology</jtitle><addtitle>Front Pharmacol</addtitle><date>2024-04-17</date><risdate>2024</risdate><volume>15</volume><spage>1398381</spage><pages>1398381-</pages><issn>1663-9812</issn><eissn>1663-9812</eissn><abstract>Cardiovascular diseases (CVDs) are currently the leading cause of death worldwide. In 2022, the CVDs contributed to 19.8 million deaths globally, accounting for one-third of all global deaths. With an aging population and changing lifestyles, CVDs pose a major threat to human health. Mitochondria-associated endoplasmic reticulum membranes (MAMs) are communication platforms between cellular organelles and regulate cellular physiological functions, including apoptosis, autophagy, and programmed necrosis. Further research has shown that MAMs play a critical role in the pathogenesis of CVDs, including myocardial ischemia and reperfusion injury, heart failure, pulmonary hypertension, and coronary atherosclerosis. This suggests that MAMs could be an important therapeutic target for managing CVDs. The goal of this study is to summarize the protein complex of MAMs, discuss its role in the pathological mechanisms of CVDs in terms of its functions such as Ca
transport, apoptotic signaling, and lipid metabolism, and suggest the possibility of MAMs as a potential therapeutic approach.</abstract><cop>Switzerland</cop><pub>Frontiers Media S.A</pub><pmid>38694924</pmid><doi>10.3389/fphar.2024.1398381</doi><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1663-9812 |
ispartof | Frontiers in pharmacology, 2024-04, Vol.15, p.1398381 |
issn | 1663-9812 1663-9812 |
language | eng |
recordid | cdi_doaj_primary_oai_doaj_org_article_11ce101561c04be3a1520f177ed3ff19 |
source | PubMed Central |
subjects | cardiovascular diseases coronary atherosclerosis mitochondria-associated endoplasmic reticulum membrane myocardial ischemia Pharmacology therapeutic target |
title | Mitochondria-associated endoplasmic reticulum membranes as a therapeutic target for cardiovascular diseases |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-18T18%3A26%3A32IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Mitochondria-associated%20endoplasmic%20reticulum%20membranes%20as%20a%20therapeutic%20target%20for%20cardiovascular%20diseases&rft.jtitle=Frontiers%20in%20pharmacology&rft.au=Ding,%20Yanqiu&rft.date=2024-04-17&rft.volume=15&rft.spage=1398381&rft.pages=1398381-&rft.issn=1663-9812&rft.eissn=1663-9812&rft_id=info:doi/10.3389/fphar.2024.1398381&rft_dat=%3Cproquest_doaj_%3E3050174819%3C/proquest_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c420t-39dc33702304e0b9718cfcdb08954160642924d731e5a6308734396990d7a7423%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=3050174819&rft_id=info:pmid/38694924&rfr_iscdi=true |