<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Murahashi M</submitter><funding>japan society for the promotion of science</funding><pagination>299-310</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8971687</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>70(4)</volume><pubmed_abstract>It is widely accepted that E-selectin, an inducible endothelial cell adhesion molecule, plays a critical role in the initial step of neutrophil recruitment to sites of acute inflammation. However, immunohistological analysis of E-selectin has been hampered by lack of E-selectin-specific monoclonal antibodies that can stain formalin-fixed, paraffin-embedded (FFPE) tissue sections. Here, we employed E-selectin•IgM (a soluble form of E-selectin) as immunogen, and then, after negative selection with L-selectin•IgM and P-selectin•IgM and screening of FFPE sections of both COS-1 cells overexpressing E-selectin and acute appendicitis tissues, we successfully generated an E-selectin-specific monoclonal antibody capable of staining FFPE tissue sections. We used this antibody, designated U12-12, to perform quantitative immunohistological analysis of 390 colonic mucosal biopsy specimens representing ulcerative colitis. We found that the higher the histological disease activity, the greater the number of vessels expressing E-selectin, an observation consistent with previous analyses of frozen tissue sections. Furthermore, in active ulcerative colitis, E-selectin-expressing vessels contained neutrophils attached to endothelial cells, presumably in the process of extravasation, which eventually could cause epithelial damage. These results overall indicate that U12-12 is effective for E-selectin immunohistochemistry in archived FFPE samples representing various human diseases.</pubmed_abstract><journal>The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society</journal><pubmed_title>Vascular E-selectin Expression Detected in Formalin-fixed, Paraffin-embedded Sections With an E-selectin Monoclonal Antibody Correlates With Ulcerative Colitis Activity.</pubmed_title><pmcid>PMC8971687</pmcid><funding_grant_id>21H02702</funding_grant_id><pubmed_authors>Kogami A</pubmed_authors><pubmed_authors>Nagaya T</pubmed_authors><pubmed_authors>Muramoto A</pubmed_authors><pubmed_authors>Hoshino H</pubmed_authors><pubmed_authors>Murahashi M</pubmed_authors><pubmed_authors>Akama TO</pubmed_authors><pubmed_authors>Goi T</pubmed_authors><pubmed_authors>Kobayashi M</pubmed_authors><pubmed_authors>Hirayama A</pubmed_authors><pubmed_authors>Okamura T</pubmed_authors><pubmed_authors>Mitoma J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Vascular E-selectin Expression Detected in Formalin-fixed, Paraffin-embedded Sections With an E-selectin Monoclonal Antibody Correlates With Ulcerative Colitis Activity.</name><description>It is widely accepted that E-selectin, an inducible endothelial cell adhesion molecule, plays a critical role in the initial step of neutrophil recruitment to sites of acute inflammation. However, immunohistological analysis of E-selectin has been hampered by lack of E-selectin-specific monoclonal antibodies that can stain formalin-fixed, paraffin-embedded (FFPE) tissue sections. Here, we employed E-selectin•IgM (a soluble form of E-selectin) as immunogen, and then, after negative selection with L-selectin•IgM and P-selectin•IgM and screening of FFPE sections of both COS-1 cells overexpressing E-selectin and acute appendicitis tissues, we successfully generated an E-selectin-specific monoclonal antibody capable of staining FFPE tissue sections. We used this antibody, designated U12-12, to perform quantitative immunohistological analysis of 390 colonic mucosal biopsy specimens representing ulcerative colitis. We found that the higher the histological disease activity, the greater the number of vessels expressing E-selectin, an observation consistent with previous analyses of frozen tissue sections. Furthermore, in active ulcerative colitis, E-selectin-expressing vessels contained neutrophils attached to endothelial cells, presumably in the process of extravasation, which eventually could cause epithelial damage. These results overall indicate that U12-12 is effective for E-selectin immunohistochemistry in archived FFPE samples representing various human diseases.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Apr</publication><modification>2024-11-21T05:41:34.843Z</modification><creation>2024-11-21T05:41:34.843Z</creation></dates><accession>S-EPMC8971687</accession><cross_references><pubmed>35253509</pubmed><doi>10.1369/00221554221085336</doi></cross_references></HashMap>