<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Carter SD</submitter><funding>National Center for Research Resources</funding><funding>NIDA NIH HHS</funding><funding>NCRR NIH HHS</funding><funding>NIA NIH HHS</funding><funding>Howard Hughes Medical Institute</funding><funding>NIAID NIH HHS</funding><funding>Louis V. Gerstner Jr., Scholars Program</funding><funding>National Institute of General Medical Sciences</funding><funding>National Institute on Aging</funding><funding>AEI/FEDER</funding><funding>Leon Levy Foundation</funding><funding>European Research Council</funding><funding>U.S. Department of Defense</funding><funding>Israel Science Foundation</funding><funding>NINDS NIH HHS</funding><funding>NCI NIH HHS</funding><funding>Ministerio de Economía y Competitividad</funding><funding>National Institute on Drug Abuse</funding><funding>Pittsburgh Foundation</funding><funding>NIGMS NIH HHS</funding><funding>NIH HHS</funding><funding>National Science Foundation</funding><pagination>eaay9572</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7112762</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>6(14)</volume><pubmed_abstract>The endoplasmic reticulum (ER) is a highly dynamic network of membranes. Here, we combine live-cell microscopy with in situ cryo-electron tomography to directly visualize ER dynamics in several secretory cell types including pancreatic β-cells and neurons under near-native conditions. Using these imaging approaches, we identify a novel, mobile form of ER, ribosome-associated vesicles (RAVs), found primarily in the cell periphery, which is conserved across different cell types and species. We show that RAVs exist as distinct, highly dynamic structures separate from the intact ER reticular architecture that interact with mitochondria via direct intermembrane contacts. These findings describe a new ER subcompartment within cells.</pubmed_abstract><journal>Science advances</journal><pubmed_title>Ribosome-associated vesicles: A dynamic subcompartment of the endoplasmic reticulum in secretory cells.</pubmed_title><pmcid>PMC7112762</pmcid><funding_grant_id>P50 AI150464</funding_grant_id><funding_grant_id>P41 RR001209</funding_grant_id><funding_grant_id>R01 AG056387</funding_grant_id><funding_grant_id>MCB-1408986</funding_grant_id><funding_grant_id>BIO2016-76400-R</funding_grant_id><funding_grant_id>S10 RR019003</funding_grant_id><funding_grant_id>R56 AG058593</funding_grant_id><funding_grant_id>P30 CA013696</funding_grant_id><funding_grant_id>K01 AG045335</funding_grant_id><funding_grant_id>P50GM082545</funding_grant_id><funding_grant_id>K08 DA031241</funding_grant_id><funding_grant_id>P41 GM103310</funding_grant_id><funding_grant_id>R35 GM122588</funding_grant_id><funding_grant_id>S10 RR025488</funding_grant_id><funding_grant_id>1S10RR016236</funding_grant_id><funding_grant_id>S10 RR029300</funding_grant_id><funding_grant_id>K08DA031241</funding_grant_id><funding_grant_id>1S10RR019003</funding_grant_id><funding_grant_id>1285/14</funding_grant_id><funding_grant_id>S10 OD016236</funding_grant_id><funding_grant_id>1S10RR025488</funding_grant_id><funding_grant_id>R01 GM029169</funding_grant_id><funding_grant_id>R37 GM029169</funding_grant_id><funding_grant_id>PR141292</funding_grant_id><funding_grant_id>F30 NS093798</funding_grant_id><funding_grant_id>AIC-A-2011-0638</funding_grant_id><funding_grant_id>K01AG045335</funding_grant_id><funding_grant_id>310649</funding_grant_id><funding_grant_id>GM29169</funding_grant_id><funding_grant_id>P50 GM082545</funding_grant_id><pubmed_authors>Morgenstern TJ</pubmed_authors><pubmed_authors>Aslanoglou D</pubmed_authors><pubmed_authors>Wolf SG</pubmed_authors><pubmed_authors>Mitchell WG</pubmed_authors><pubmed_authors>Jensen GJ</pubmed_authors><pubmed_authors>Eisenman L</pubmed_authors><pubmed_authors>Carter SD</pubmed_authors><pubmed_authors>Wills ZP</pubmed_authors><pubmed_authors>Balla T</pubmed_authors><pubmed_authors>Calderon MJ</pubmed_authors><pubmed_authors>Rice WJ</pubmed_authors><pubmed_authors>Pilli J</pubmed_authors><pubmed_authors>Langlois R</pubmed_authors><pubmed_authors>Levy ES</pubmed_authors><pubmed_authors>Frank J</pubmed_authors><pubmed_authors>Freyberg RJ</pubmed_authors><pubmed_authors>Javitch JA</pubmed_authors><pubmed_authors>Fass D</pubmed_authors><pubmed_authors>Aguilar JI</pubmed_authors><pubmed_authors>Farino ZJ</pubmed_authors><pubmed_authors>Courel M</pubmed_authors><pubmed_authors>Hampton CM</pubmed_authors><pubmed_authors>Grassucci RA</pubmed_authors><pubmed_authors>Freyberg Z</pubmed_authors><pubmed_authors>Aridor M</pubmed_authors><pubmed_authors>Shiva S</pubmed_authors><pubmed_authors>Bartolini F</pubmed_authors><pubmed_authors>Greenberg NL</pubmed_authors><pubmed_authors>Fish KN</pubmed_authors><pubmed_authors>Volchuk A</pubmed_authors><pubmed_authors>Walter P</pubmed_authors><pubmed_authors>Li W</pubmed_authors><pubmed_authors>Wigge C</pubmed_authors><pubmed_authors>Carazo JM</pubmed_authors><pubmed_authors>Tran NH</pubmed_authors><pubmed_authors>Murray SA</pubmed_authors><pubmed_authors>Wallace CT</pubmed_authors><pubmed_authors>Siegmund SE</pubmed_authors><pubmed_authors>George EW</pubmed_authors><pubmed_authors>Watkins SC</pubmed_authors><pubmed_authors>Pemberton J</pubmed_authors><pubmed_authors>Area-Gomez E</pubmed_authors><pubmed_authors>Melero R</pubmed_authors><pubmed_authors>Yi E</pubmed_authors></additional><is_claimable>false</is_claimable><name>Ribosome-associated vesicles: A dynamic subcompartment of the endoplasmic reticulum in secretory cells.</name><description>The endoplasmic reticulum (ER) is a highly dynamic network of membranes. Here, we combine live-cell microscopy with in situ cryo-electron tomography to directly visualize ER dynamics in several secretory cell types including pancreatic β-cells and neurons under near-native conditions. Using these imaging approaches, we identify a novel, mobile form of ER, ribosome-associated vesicles (RAVs), found primarily in the cell periphery, which is conserved across different cell types and species. We show that RAVs exist as distinct, highly dynamic structures separate from the intact ER reticular architecture that interact with mitochondria via direct intermembrane contacts. These findings describe a new ER subcompartment within cells.</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Apr</publication><modification>2026-05-07T07:26:11.979Z</modification><creation>2020-05-22T16:25:17Z</creation></dates><accession>S-EPMC7112762</accession><cross_references><pubmed>32270040</pubmed><doi>10.1126/sciadv.aay9572</doi></cross_references></HashMap>