<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Yamamoto T</submitter><funding>Japan Society for the Promotion of Science</funding><pagination>e0281746</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9937502</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>18(2)</volume><pubmed_abstract>The apoptosis-associated speck-like protein containing a caspase recruitment domain (ASC)/caspase-1/interleukin(IL)-1β axis, also known as the inflammasome pathway, is indispensable for IL-1β activation in response to various pathogens or own damages. Previously, we developed an NLRP3-inflammasome using a cell-free system and identified ASC targeting drugs; thus, examination of ASC-related histopathology in various diseases could help to provide indications for these drugs. Here, we generated mice deficient only in ASC-protein (ASC-deficient (AD) mice) using CRISPR/Cas9 technology, studied which tissues were most affected, and obtained histopathological images of lipopolysaccharide (LPS)-induced endotoxemia. C57BL/6 wild-type (WT) and (AD) mice were injected intraperitoneally with a lethal</pubmed_abstract><journal>PloS one</journal><pubmed_title>Intestinal edema induced by LPS-induced endotoxemia is associated with an inflammasome adaptor ASC.</pubmed_title><pmcid>PMC9937502</pmcid><funding_grant_id>20H03719, 22K19438</funding_grant_id><funding_grant_id>20K07376</funding_grant_id><pubmed_authors>Kaneko N</pubmed_authors><pubmed_authors>Kurata M</pubmed_authors><pubmed_authors>Masumoto J</pubmed_authors><pubmed_authors>Yamamoto T</pubmed_authors></additional><is_claimable>false</is_claimable><name>Intestinal edema induced by LPS-induced endotoxemia is associated with an inflammasome adaptor ASC.</name><description>The apoptosis-associated speck-like protein containing a caspase recruitment domain (ASC)/caspase-1/interleukin(IL)-1β axis, also known as the inflammasome pathway, is indispensable for IL-1β activation in response to various pathogens or own damages. Previously, we developed an NLRP3-inflammasome using a cell-free system and identified ASC targeting drugs; thus, examination of ASC-related histopathology in various diseases could help to provide indications for these drugs. Here, we generated mice deficient only in ASC-protein (ASC-deficient (AD) mice) using CRISPR/Cas9 technology, studied which tissues were most affected, and obtained histopathological images of lipopolysaccharide (LPS)-induced endotoxemia. C57BL/6 wild-type (WT) and (AD) mice were injected intraperitoneally with a lethal</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023</publication><modification>2025-04-04T23:12:24.355Z</modification><creation>2025-04-04T23:12:24.355Z</creation></dates><accession>S-EPMC9937502</accession><cross_references><pubmed>36800329</pubmed><doi>10.1371/journal.pone.0281746</doi></cross_references></HashMap>