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dc.contributor.authorCote, Lauren Esther
dc.contributor.authorSimental, Eric
dc.contributor.authorReddien, Peter
dc.date.accessioned2020-07-30T01:24:42Z
dc.date.available2020-07-30T01:24:42Z
dc.date.issued2019-04
dc.date.submitted2018-11
dc.identifier.issn2041-1723
dc.identifier.urihttps://hdl.handle.net/1721.1/126442
dc.description.abstractRegeneration and tissue turnover require new cell production and positional information. Planarians are flatworms capable of regenerating all body parts using a population of stem cells called neoblasts. The positional information required for tissue patterning is primarily harbored by muscle cells, which also control body contraction. Here we produce an in silico planarian matrisome and use recent whole-animal single-cell-transcriptome data to determine that muscle is a major source of extracellular matrix (ECM). No other ECM-secreting, fibroblast-like cell type was detected. Instead, muscle cells express core ECM components, including all 19 collagen-encoding genes. Inhibition of muscle-expressed hemicentin-1 (hmcn-1), which encodes a highly conserved ECM glycoprotein, results in ectopic peripheral localization of cells, including neoblasts, outside of the muscle layer. ECM secretion and hmcn-1-dependent maintenance of tissue separation indicate that muscle functions as a planarian connective tissue, raising the possibility of broad roles for connective tissue in adult positional information.en_US
dc.language.isoen
dc.publisherSpringer Science and Business Media LLCen_US
dc.relation.isversionofhttp://dx.doi.org/10.1038/s41467-019-09539-6en_US
dc.rightsCreative Commons Attribution 4.0 International licenseen_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.sourceNatureen_US
dc.titleMuscle functions as a connective tissue and source of extracellular matrix in planariansen_US
dc.typeArticleen_US
dc.identifier.citationCote, Lauren E. et al. "Muscle functions as a connective tissue and source of extracellular matrix in planarians." Nature Communications 10 (April 2019): 1592 © 2019 The Author(s)en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.relation.journalNature Communicationsen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2019-07-18T14:28:23Z
dspace.date.submission2019-07-18T14:28:24Z
mit.journal.volume10en_US
mit.journal.issue1en_US
mit.metadata.statusComplete


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