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dc.contributor.authorFarwell, Alan P.
dc.contributor.authorDubord-Tomasetti, Susan A.
dc.date2022-08-11T08:10:02.000
dc.date.accessioned2022-08-23T16:52:52Z
dc.date.available2022-08-23T16:52:52Z
dc.date.issued1999-10-28
dc.date.submitted2008-07-09
dc.identifier.citation<p>Endocrinology. 1999 Nov;140(11):5014-21.</p>
dc.identifier.issn0013-7227 (Print)
dc.identifier.pmid10537126
dc.identifier.urihttp://hdl.handle.net/20.500.14038/42143
dc.description.abstractAstrocytes produce laminin, a key extracellular matrix guidance molecule in the developing brain. Laminin is bound to transmembrane receptors on the surface of astrocytes known as integrins, which are, in turn, bound to the microfilament meshwork inside the astrocyte. Previous studies have shown that T4 regulates the pattern of integrin distribution in astrocytes by modulating the organization of the microfilaments. In this study, the effect of thyroid hormone on the secretion and topology of laminin in astrocytes was examined. Linear arrays of secreted laminin were observed on the surface of the T4-treated astrocytes within 10 h after seeding the cells onto poly-D-lysine-coated coverslips and became an organized meshwork by 24 h. In contrast, little if any laminin was identified on the surface of either hormone-deficient or T3-treated cells until 36 h after seeding and then was restricted to punctate deposits. Secretion of laminin into the medium by hormone-deficient and T3-treated cells was significantly greater than that by T4-treated cells. Conversely, deposition of laminin into the extracellular matrix was significantly greater in T4-treated cells than in hormone-deficient and T3-treated cells. Thyroid hormone had no effect on the production of laminin by astrocytes. These data show that T4 regulates the extracellular deposition and organization of laminin on the surface of astrocytes and provide a mechanism by which this morphogenic hormone can influence neuronal migration and axonal projection in the developing brain.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=10537126&dopt=Abstract">Link to Article in PubMed</a></p>
dc.relation.urlhttps://doi.org/10.1210/en.140.11.5014
dc.subjectAnimals
dc.subjectAnimals, Newborn
dc.subjectAstrocytes
dc.subjectCells, Cultured
dc.subjectElectrophoresis, Polyacrylamide Gel
dc.subjectExtracellular Matrix
dc.subjectImmunohistochemistry
dc.subjectImmunosorbent Techniques
dc.subjectLaminin
dc.subjectMice
dc.subjectMicroscopy, Fluorescence
dc.subjectRats
dc.subjectSarcoma, Experimental
dc.subjectThyroid Hormones
dc.subjectThyroxine
dc.subjectTriiodothyronine
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.titleThyroid hormone regulates the extracellular organization of laminin on astrocytes
dc.typeJournal Article
dc.source.journaltitleEndocrinology
dc.source.volume140
dc.source.issue11
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/oapubs/517
dc.identifier.contextkey544999
html.description.abstract<p>Astrocytes produce laminin, a key extracellular matrix guidance molecule in the developing brain. Laminin is bound to transmembrane receptors on the surface of astrocytes known as integrins, which are, in turn, bound to the microfilament meshwork inside the astrocyte. Previous studies have shown that T4 regulates the pattern of integrin distribution in astrocytes by modulating the organization of the microfilaments. In this study, the effect of thyroid hormone on the secretion and topology of laminin in astrocytes was examined. Linear arrays of secreted laminin were observed on the surface of the T4-treated astrocytes within 10 h after seeding the cells onto poly-D-lysine-coated coverslips and became an organized meshwork by 24 h. In contrast, little if any laminin was identified on the surface of either hormone-deficient or T3-treated cells until 36 h after seeding and then was restricted to punctate deposits. Secretion of laminin into the medium by hormone-deficient and T3-treated cells was significantly greater than that by T4-treated cells. Conversely, deposition of laminin into the extracellular matrix was significantly greater in T4-treated cells than in hormone-deficient and T3-treated cells. Thyroid hormone had no effect on the production of laminin by astrocytes. These data show that T4 regulates the extracellular deposition and organization of laminin on the surface of astrocytes and provide a mechanism by which this morphogenic hormone can influence neuronal migration and axonal projection in the developing brain.</p>
dc.identifier.submissionpathoapubs/517
dc.contributor.departmentMolecular Endocrinology Laboratory
dc.source.pages5014-21


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