<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhuang J</submitter><funding>the Guangdong Medical Research Fund</funding><funding>the Open project of the Key Laboratory of Male Reproduction and Genetics of the National Health Commission</funding><funding>Guangdong Basic and Applied Basic Research Foundation</funding><funding>Basic and Applied Basic Research Foundation of Guangdong Province</funding><funding>National Natural Science Foundation of China</funding><funding>Guangdong Provincial Reproductive Science Institute Innovation Team grants</funding><pagination>21</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10173474</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>20(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Morphological and functional alterations in aging reproductive organs result in decreased male fertility. The epididymis functions as the transition region for post-testicular sperm maturation. And we have previously demonstrated that the epididymal initial segment (IS), a region of the reproductive tract essential for sperm maturation and capacitation, undergoes considerable histological changes and chronic immune activation in mice during aging. However, the local aging-associated cellular and molecular changes in the aged epididymal IS are poorly understood.&lt;h4>Results&lt;/h4>We conducted single-cell RNA sequencing analysis on the epididymal IS of young (3-month-old) and old (21-month-old) mice. In total, 10,027 cells from the epididymal IS tissues of young and old mice </pubmed_abstract><journal>Immunity &amp; ageing : I &amp; A</journal><pubmed_title>Single-cell RNA sequencing reveals the local cell landscape in mouse epididymal initial segment during aging.</pubmed_title><pmcid>PMC10173474</pmcid><funding_grant_id>KF202001</funding_grant_id><funding_grant_id>Nos. 2020A1515111160, 2021A1515110986 and 2020A1515110735</funding_grant_id><funding_grant_id>No.C-03</funding_grant_id><funding_grant_id>Nos. B2021333 and B2021453</funding_grant_id><funding_grant_id>Nos.82101819 and 82101664</funding_grant_id><pubmed_authors>Liu H</pubmed_authors><pubmed_authors>Li X</pubmed_authors><pubmed_authors>Yao J</pubmed_authors><pubmed_authors>Liu J</pubmed_authors><pubmed_authors>Hu Y</pubmed_authors><pubmed_authors>Xie Y</pubmed_authors><pubmed_authors>Qin W</pubmed_authors><pubmed_authors>Sun X</pubmed_authors><pubmed_authors>Zhuang J</pubmed_authors><pubmed_authors>Nie H</pubmed_authors><pubmed_authors>Tu X</pubmed_authors></additional><is_claimable>false</is_claimable><name>Single-cell RNA sequencing reveals the local cell landscape in mouse epididymal initial segment during aging.</name><description>&lt;h4>Background&lt;/h4>Morphological and functional alterations in aging reproductive organs result in decreased male fertility. The epididymis functions as the transition region for post-testicular sperm maturation. And we have previously demonstrated that the epididymal initial segment (IS), a region of the reproductive tract essential for sperm maturation and capacitation, undergoes considerable histological changes and chronic immune activation in mice during aging. However, the local aging-associated cellular and molecular changes in the aged epididymal IS are poorly understood.&lt;h4>Results&lt;/h4>We conducted single-cell RNA sequencing analysis on the epididymal IS of young (3-month-old) and old (21-month-old) mice. In total, 10,027 cells from the epididymal IS tissues of young and old mice </description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 May</publication><modification>2025-04-22T14:40:07.587Z</modification><creation>2025-04-06T01:07:58.223Z</creation></dates><accession>S-EPMC10173474</accession><cross_references><pubmed>37170325</pubmed><doi>10.1186/s12979-023-00345-9</doi></cross_references></HashMap>