{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Bartosh TJ"],"funding":["NCRR NIH HHS","NIH","Cancer Prevention and Research Institute of Texas","NIH HHS"],"pagination":["2443-56"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC3834191"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["31(11)"],"pubmed_abstract":["Human mesenchymal stem/precursor cells (MSC) are similar to some other stem/progenitor cells in that they compact into spheres when cultured in hanging drops or on nonadherent surfaces. Assembly of MSC into spheres alters many of their properties, including enhanced secretion of factors that mediate inflammatory and immune responses. Here we demonstrated that MSC spontaneously aggregated into sphere-like structures after injection into a subcutaneous air pouch or the peritoneum of mice. The structures were similar to MSC spheres formed in cultures demonstrated by the increased expression of genes for inflammation-modulating factors TSG6, STC1, and COX2, a key enzyme in production of PGE2. To identify the signaling pathways involved, hanging drop cultures were used to follow the time-depend"],"journal":["Stem cells (Dayton, Ohio)"],"pubmed_title":["Dynamic compaction of human mesenchymal stem/precursor cells into spheres self-activates caspase-dependent IL1 signaling to enhance secretion of modulators of inflammation and immunity (PGE2, TSG6, and STC1)."],"pmcid":["PMC3834191"],"funding_grant_id":["P40 OD011050","P40 RR017447","RP110553-P1","P40RR17447"],"pubmed_authors":["Kuhlman J","Bazhanov N","Bartosh TJ","Ylostalo JH","Prockop DJ"],"additional_accession":[]},"is_claimable":false,"name":"Dynamic compaction of human mesenchymal stem/precursor cells into spheres self-activates caspase-dependent IL1 signaling to enhance secretion of modulators of inflammation and immunity (PGE2, TSG6, and STC1).","description":"Human mesenchymal stem/precursor cells (MSC) are similar to some other stem/progenitor cells in that they compact into spheres when cultured in hanging drops or on nonadherent surfaces. Assembly of MSC into spheres alters many of their properties, including enhanced secretion of factors that mediate inflammatory and immune responses. Here we demonstrated that MSC spontaneously aggregated into sphere-like structures after injection into a subcutaneous air pouch or the peritoneum of mice. The structures were similar to MSC spheres formed in cultures demonstrated by the increased expression of genes for inflammation-modulating factors TSG6, STC1, and COX2, a key enzyme in production of PGE2. To identify the signaling pathways involved, hanging drop cultures were used to follow the time-depend","dates":{"release":"2013-01-01T00:00:00Z","publication":"2013 Nov","modification":"2026-05-29T19:34:15.205Z","creation":"2019-03-27T03:08:55Z"},"accession":"S-EPMC3834191","cross_references":{"pubmed":["23922312"],"doi":["10.1002/stem.1499"]}}