<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>7(2)</volume><submitter>Liao J</submitter><pubmed_abstract>Macrophage colony-stimulating factor (M-CSF) is an important cytokine for monocyte/macrophage lineage. Secretory M-CSF (sM-CSF) and membrane-bound M-CSF (mM-CSF) are two major alternative splicing isoforms. The functional diversity of these isoforms in the activation of tumor-associated macrophages (TAMs), especially in lymphoma microenvironment, has not been documented. Here, we studied the effects of M-CSF isoforms on TAMs in xenograft mouse model. More infiltrating TAMs were detected in microenvironment with mM-CSF and sM-CSF. TAMs could be divided into three subpopulations based on their expression of CD206 and Ly6C. While sM-CSF had greater potential to recruit and induce differentiation of TAMs and TAM subpopulations, mM-CSF had greater potential to induce proliferation of TAMs and T</pubmed_abstract><journal>Oncotarget</journal><pagination>1354-66</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4811465</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Diverse in vivo effects of soluble and membrane-bound M-CSF on tumor-associated macrophages in lymphoma xenograft model.</pubmed_title><pmcid>PMC4811465</pmcid><pubmed_authors>Liao J</pubmed_authors><pubmed_authors>Yang X</pubmed_authors><pubmed_authors>Ma S</pubmed_authors><pubmed_authors>Wang R</pubmed_authors><pubmed_authors>Feng W</pubmed_authors><pubmed_authors>Lin Y</pubmed_authors><pubmed_authors>Zheng G</pubmed_authors><pubmed_authors>Yang F</pubmed_authors><pubmed_authors>Wang L</pubmed_authors><pubmed_authors>Ren Q</pubmed_authors></additional><is_claimable>false</is_claimable><name>Diverse in vivo effects of soluble and membrane-bound M-CSF on tumor-associated macrophages in lymphoma xenograft model.</name><description>Macrophage colony-stimulating factor (M-CSF) is an important cytokine for monocyte/macrophage lineage. Secretory M-CSF (sM-CSF) and membrane-bound M-CSF (mM-CSF) are two major alternative splicing isoforms. The functional diversity of these isoforms in the activation of tumor-associated macrophages (TAMs), especially in lymphoma microenvironment, has not been documented. Here, we studied the effects of M-CSF isoforms on TAMs in xenograft mouse model. More infiltrating TAMs were detected in microenvironment with mM-CSF and sM-CSF. TAMs could be divided into three subpopulations based on their expression of CD206 and Ly6C. While sM-CSF had greater potential to recruit and induce differentiation of TAMs and TAM subpopulations, mM-CSF had greater potential to induce proliferation of TAMs and T</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Jan</publication><modification>2025-04-22T12:07:15.707Z</modification><creation>2019-03-27T03:10:32Z</creation></dates><accession>S-EPMC4811465</accession><cross_references><pubmed>26595525</pubmed><doi>10.18632/oncotarget.6362</doi></cross_references></HashMap>