<HashMap><database>iProX</database><scores/><additional><omics_type>Proteomics</omics_type><submitter>Hong Liu</submitter><species>Oryctolagus Cuniculus</species><full_dataset_link>http://www.iprox.org/page/project.html?id=IPX0016072000</full_dataset_link><submitter_email>liuhongzef@263.net</submitter_email><submitter_affiliation>Shanghai Jiao Tong University</submitter_affiliation><sample_protocol></sample_protocol><repository>iProX</repository><data_protocol></data_protocol><pubmed_abstract>&lt;h4>Introduction&lt;/h4>Human amniotic epithelial cell-derived extracellular vesicles (hAEC-EVs) have shown therapeutic potential in corneal injury repair; however, the underlying molecular mechanisms, particularly those related to extracellular matrix (ECM) remodeling, remain incompletely understood.&lt;h4>Methods&lt;/h4>A proteomic and bioinformatic strategy was applied to analyze ECM-related molecular alterations in corneal tissues following alkali injury and hAEC-EV treatment. Differentially expressed ECM-related genes were identified and subjected to pathway enrichment, protein-protein interaction, and immune infiltration analyses. To enhance experimental rigor, key findings were validated at both the transcript and protein levels using quantitative real-time PCR and Western blotting. In addition, &lt;i>in vitro&lt;/i> functional assays were performed to assess the effects of hAEC-EVs on corneal epithelial and stromal cell proliferation and migration.&lt;h4>Results&lt;/h4>hAEC-EV treatment significantly upregulated ECM-stabilizing molecules, including A2M, LAMA1, and VIT, while downregulating the injury- and inflammation-associated protease CTSB at both mRNA and protein levels. Enrichment analyses revealed that hAEC-EVs modulate ECM-receptor interaction pathways and cell-ECM communication. Functional assays confirmed that hAEC-EVs directly enhance the proliferation and migration of human corneal epithelial cells and human corneal stromal cells. Immune infiltration analysis further suggested that hAEC-EVs reshape the corneal immune microenvironment toward a repair-permissive state.&lt;h4>Conclusion&lt;/h4>Through integrated proteomic, bioinformatic, protein-level validation, and functional analyses, this study demonstrates that hAEC-EVs promote corneal repair by coordinating ECM remodeling, regulating key signaling networks, and modulating immune responses, providing mechanistic support for their therapeutic application in corneal injuries.</pubmed_abstract><pubmed_title>Targeted proteomic and bioinformatic investigation of extracellular matrix remodeling in hAEC-EV-mediated corneal repair.</pubmed_title><pubmed_authors>Hu Shuqin S, Qiu Ting T, Liu Hong H</pubmed_authors></additional><is_claimable>false</is_claimable><name>Targeted proteomic and  bioinformatic investigation of  extracellular matrix remodeling in  hAEC-EV-mediated corneal repair</name><description>Human amniotic epithelial cell-derived extracellular vesicles  (hAEC-EVs) have shown therapeutic potential in corneal injury repair; however,  the underlying molecular mechanisms, particularly those related to extracellular  matrix (ECM) remodeling, remain incompletely understood.</description><dates><publication>Wed Mar 11 00:00:00 GMT 2026</publication></dates><accession>PXD075526</accession><cross_references><TAXONOMY>9986</TAXONOMY><pubmed>41929428</pubmed></cross_references></HashMap>