<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Xia C</submitter><funding>NIDDK NIH HHS</funding><funding>NIEHS NIH HHS</funding><pagination>2434-2447</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6821582</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>43(12)</volume><pubmed_abstract>&lt;h4>Objective&lt;/h4>Myeloid-related protein-14 (MRP14) and its binding partner MRP8 play an essential role in innate immune function and have been implicated in a variety of inflammatory diseases. However, the role of MRP14 in obesity-induced inflammation and insulin resistance is not well defined. This study investigated the role of MRP14 in macrophage-mediated adipose tissue inflammation and obesity-induced insulin resistance.&lt;h4>Subjects and results&lt;/h4>Wild-type (WT) and Mrp14&lt;sup>-/-&lt;/sup> mice were fed with a high-fat diet or normal chow for 12 weeks. Tissue-resident macrophages in both adipose tissue and liver from obese WT mice expressed higher levels of MRP14 in the visceral adipose fat and liver compared with the lean mice. Mrp14&lt;sup>-/-&lt;/sup> mice demonstrated a significantly impr</pubmed_abstract><journal>International journal of obesity (2005)</journal><pubmed_title>MRP14 enhances the ability of macrophage to recruit T cells and promotes obesity-induced insulin resistance.</pubmed_title><pmcid>PMC6821582</pmcid><funding_grant_id>R00 ES026241</funding_grant_id><funding_grant_id>K99 ES026241</funding_grant_id><funding_grant_id>K01 DK105108</funding_grant_id><pubmed_authors>Simon DI</pubmed_authors><pubmed_authors>Toomey AC</pubmed_authors><pubmed_authors>Zhao S</pubmed_authors><pubmed_authors>Rajagopalan S</pubmed_authors><pubmed_authors>Braunstein Z</pubmed_authors><pubmed_authors>Rao X</pubmed_authors><pubmed_authors>Mao H</pubmed_authors><pubmed_authors>Xia C</pubmed_authors><pubmed_authors>Razavi M</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Zhong J</pubmed_authors></additional><is_claimable>false</is_claimable><name>MRP14 enhances the ability of macrophage to recruit T cells and promotes obesity-induced insulin resistance.</name><description>&lt;h4>Objective&lt;/h4>Myeloid-related protein-14 (MRP14) and its binding partner MRP8 play an essential role in innate immune function and have been implicated in a variety of inflammatory diseases. However, the role of MRP14 in obesity-induced inflammation and insulin resistance is not well defined. This study investigated the role of MRP14 in macrophage-mediated adipose tissue inflammation and obesity-induced insulin resistance.&lt;h4>Subjects and results&lt;/h4>Wild-type (WT) and Mrp14&lt;sup>-/-&lt;/sup> mice were fed with a high-fat diet or normal chow for 12 weeks. Tissue-resident macrophages in both adipose tissue and liver from obese WT mice expressed higher levels of MRP14 in the visceral adipose fat and liver compared with the lean mice. Mrp14&lt;sup>-/-&lt;/sup> mice demonstrated a significantly impr</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Dec</publication><modification>2025-04-04T12:17:56.555Z</modification><creation>2019-11-09T08:01:42Z</creation></dates><accession>S-EPMC6821582</accession><cross_references><pubmed>31040394</pubmed><doi>10.1038/s41366-019-0366-4</doi></cross_references></HashMap>