<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Rodriguez-Paez L</submitter><funding>SECIHTI</funding><funding>Secretaría de Investigación y Posgrado del Instituto Politécnico Nacional</funding><pagination>11895</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12733172</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>26(24)</volume><pubmed_abstract>Autophagy is an intracellular process that recycles and degrades cytoplasmic components, including organelles and macromolecules, to provide energy and basic components for cell survival, maintain cellular homeostasis, and avoid self-damage. It is currently not fully known if mouse sperm undergoes the autophagy process, nor is the subcellular distribution, protein levels of autophagy-related proteins, and the biological role of autophagy in epididymal mouse sperm physiology fully understood. We aimed to investigate key autophagy markers, including LC3 (microtubule-associated protein 1A/1B-light chain 3), p62/SQSTM1 (Sequestosome 1), and mTOR (mechanistic Target of Rapamycin), in epididymal mouse sperm under capacitation (Cap) or non-capacitation (NC) conditions. Furthermore, we evaluated t</pubmed_abstract><journal>International journal of molecular sciences</journal><pubmed_title>Autophagy-Related Proteins Influence Mouse Epididymal Sperm Motility.</pubmed_title><pmcid>PMC12733172</pmcid><funding_grant_id>95426</funding_grant_id><funding_grant_id>53185</funding_grant_id><funding_grant_id>6630</funding_grant_id><funding_grant_id>65406</funding_grant_id><funding_grant_id>20253438</funding_grant_id><funding_grant_id>11644</funding_grant_id><pubmed_authors>Rodriguez-Paez L</pubmed_authors><pubmed_authors>Magana JJ</pubmed_authors><pubmed_authors>Cordero-Martinez J</pubmed_authors><pubmed_authors>Aguirre-Alvarado C</pubmed_authors><pubmed_authors>Chamorro-Cevallos G</pubmed_authors><pubmed_authors>Rosales-Cruz E</pubmed_authors><pubmed_authors>Cristobal-Luna JM</pubmed_authors><pubmed_authors>Jimenez-Gutierrez GE</pubmed_authors><pubmed_authors>Alcantara-Farfan V</pubmed_authors><pubmed_authors>Reyes-Maldonado E</pubmed_authors></additional><is_claimable>false</is_claimable><name>Autophagy-Related Proteins Influence Mouse Epididymal Sperm Motility.</name><description>Autophagy is an intracellular process that recycles and degrades cytoplasmic components, including organelles and macromolecules, to provide energy and basic components for cell survival, maintain cellular homeostasis, and avoid self-damage. It is currently not fully known if mouse sperm undergoes the autophagy process, nor is the subcellular distribution, protein levels of autophagy-related proteins, and the biological role of autophagy in epididymal mouse sperm physiology fully understood. We aimed to investigate key autophagy markers, including LC3 (microtubule-associated protein 1A/1B-light chain 3), p62/SQSTM1 (Sequestosome 1), and mTOR (mechanistic Target of Rapamycin), in epididymal mouse sperm under capacitation (Cap) or non-capacitation (NC) conditions. Furthermore, we evaluated t</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Dec</publication><modification>2026-06-04T03:20:27.699Z</modification><creation>2026-06-04T03:12:26.284Z</creation></dates><accession>S-EPMC12733172</accession><cross_references><pubmed>41465325</pubmed><doi>10.3390/ijms262411895</doi></cross_references></HashMap>