<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Li W</submitter><funding>NEI NIH HHS</funding><pagination>17-41</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10834862</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>30</volume><pubmed_abstract>&lt;h4>Purpose&lt;/h4>The conserved miR-183/96/182 cluster (miR-183C) regulates both corneal sensory innervation and corneal resident immune cells (CRICs). This study is to uncover its role in CRICs and in shaping the corneal cellular landscape at a single-cell (sc) level.&lt;h4>Methods&lt;/h4>Corneas of naïve, young adult [2 and 6 months old (mo)], female miR-183C knockout (KO) mice and wild-type (WT) littermates were harvested and dissociated into single cells. Dead cells were removed using a Dead Cell Removal kit. CD45&lt;sup>+&lt;/sup> CRICs were enriched by Magnetic Activated Cell Sorting (MACS). scRNA libraries were constructed and sequenced followed by comprehensive bioinformatic analyses.&lt;h4>Results&lt;/h4>The composition of major cell types of the cornea stays relatively stable in WT mice from 2 to 6 </pubmed_abstract><journal>The ocular surface</journal><pubmed_title>The miR-183/96/182 cluster is a checkpoint for resident immune cells and shapes the cellular landscape of the cornea.</pubmed_title><pmcid>PMC10834862</pmcid><funding_grant_id>R01 EY026059</funding_grant_id><funding_grant_id>P30 EY004068</funding_grant_id><funding_grant_id>R01 EY016058</funding_grant_id><pubmed_authors>Li W</pubmed_authors><pubmed_authors>Gurdziel K</pubmed_authors><pubmed_authors>Pitchaikannu A</pubmed_authors><pubmed_authors>Hazlett LD</pubmed_authors><pubmed_authors>Xu S</pubmed_authors><pubmed_authors>Gupta N</pubmed_authors></additional><is_claimable>false</is_claimable><name>The miR-183/96/182 cluster is a checkpoint for resident immune cells and shapes the cellular landscape of the cornea.</name><description>&lt;h4>Purpose&lt;/h4>The conserved miR-183/96/182 cluster (miR-183C) regulates both corneal sensory innervation and corneal resident immune cells (CRICs). This study is to uncover its role in CRICs and in shaping the corneal cellular landscape at a single-cell (sc) level.&lt;h4>Methods&lt;/h4>Corneas of naïve, young adult [2 and 6 months old (mo)], female miR-183C knockout (KO) mice and wild-type (WT) littermates were harvested and dissociated into single cells. Dead cells were removed using a Dead Cell Removal kit. CD45&lt;sup>+&lt;/sup> CRICs were enriched by Magnetic Activated Cell Sorting (MACS). scRNA libraries were constructed and sequenced followed by comprehensive bioinformatic analyses.&lt;h4>Results&lt;/h4>The composition of major cell types of the cornea stays relatively stable in WT mice from 2 to 6 </description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Oct</publication><modification>2025-04-18T12:53:59.124Z</modification><creation>2025-04-06T22:17:36.259Z</creation></dates><accession>S-EPMC10834862</accession><cross_references><pubmed>37536656</pubmed><doi>10.1016/j.jtos.2023.07.012</doi></cross_references></HashMap>