<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Dong S</submitter><funding>NIA NIH HHS</funding><funding>NIDDK NIH HHS</funding><funding>NCI NIH HHS</funding><funding>NINDS NIH HHS</funding><pagination>645</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6994528</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11(1)</volume><pubmed_abstract>Autophagy malfunctioning occurs in multiple human disorders, making attractive the idea of chemically modulating it with therapeutic purposes. However, for many types of autophagy, a clear understanding of tissue-specific differences in their activity and regulation is missing because of lack of methods to monitor these processes in vivo. Chaperone-mediated autophagy (CMA) is a selective type of autophagy that until now has only been studied in vitro and not in the tissue context at single cell resolution. Here, we develop a transgenic reporter mouse that allows dynamic measurement of CMA activity in vivo using image-based procedures. We identify previously unknown spatial and temporal differences in CMA activity in multiple organs and in response to stress. We illustrate the versatility o</pubmed_abstract><journal>Nature communications</journal><pubmed_title>Monitoring spatiotemporal changes in chaperone-mediated autophagy in vivo.</pubmed_title><pmcid>PMC6994528</pmcid><funding_grant_id>P30 AG038072</funding_grant_id><funding_grant_id>R01 DK124308</funding_grant_id><funding_grant_id>U54 NS100717</funding_grant_id><funding_grant_id>RF1 AG054108</funding_grant_id><funding_grant_id>R37 AG021904</funding_grant_id><funding_grant_id>K22 CA196750</funding_grant_id><funding_grant_id>P01 AG031782</funding_grant_id><funding_grant_id>R01 DK098408</funding_grant_id><pubmed_authors>Scrivo A</pubmed_authors><pubmed_authors>Cuervo AM</pubmed_authors><pubmed_authors>Bravo-Cordero JJ</pubmed_authors><pubmed_authors>Eliscovich C</pubmed_authors><pubmed_authors>Aguirre-Hernandez C</pubmed_authors><pubmed_authors>Arias E</pubmed_authors><pubmed_authors>Dong S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Monitoring spatiotemporal changes in chaperone-mediated autophagy in vivo.</name><description>Autophagy malfunctioning occurs in multiple human disorders, making attractive the idea of chemically modulating it with therapeutic purposes. However, for many types of autophagy, a clear understanding of tissue-specific differences in their activity and regulation is missing because of lack of methods to monitor these processes in vivo. Chaperone-mediated autophagy (CMA) is a selective type of autophagy that until now has only been studied in vitro and not in the tissue context at single cell resolution. Here, we develop a transgenic reporter mouse that allows dynamic measurement of CMA activity in vivo using image-based procedures. We identify previously unknown spatial and temporal differences in CMA activity in multiple organs and in response to stress. We illustrate the versatility o</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Jan</publication><modification>2025-04-27T03:58:42.845Z</modification><creation>2020-05-22T09:31:54Z</creation></dates><accession>S-EPMC6994528</accession><cross_references><pubmed>32005807</pubmed><doi>10.1038/s41467-019-14164-4</doi></cross_references></HashMap>