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dc.contributor.authorMedlock, Eugene S.
dc.contributor.authorMigita, Russell T.
dc.contributor.authorTrebasky, Lisa D.
dc.contributor.authorHousman, Jerry M.
dc.contributor.authorElliott, Gary S.
dc.contributor.authorHendren, R. Wayne
dc.contributor.authorDeprince, Randolph B.
dc.contributor.authorGreiner, Dale L.
dc.date2022-08-11T08:09:40.000
dc.date.accessioned2022-08-23T16:39:38Z
dc.date.available2022-08-23T16:39:38Z
dc.date.issued1992-01-01
dc.date.submitted2012-03-29
dc.identifier.citationDev Immunol. 1992;3(1):35-44.
dc.identifier.issn1026-7905 (Linking)
dc.identifier.pmid1285280
dc.identifier.pmid1285280
dc.identifier.urihttp://hdl.handle.net/20.500.14038/39516
dc.description.abstractCytokine regulation of prethymic T-lymphoid progenitor-cell proliferation and/or differentiation has not been well-defined, although much is known of cytokine regulation of hemopoietic stem- and progenitor-cell development. Here we use a recently identified hemopoietic growth factor, stem-cell factor (SCF) (a form of the c-kit ligand), and a transplant model of thymocyte regeneration to assess the effect of SCF on the in vivo generation of prethymic, thymocyte progenitor-cell activity. We show that recombinant rat SCF (rrSCF164) administered to weanling rats selectively induces an increase in thymocyte progenitor activity in the spleens of treated rats as compared to rats treated with vehicle, polyethylene glycol (PEG)-conjugated rat albumin, or recombinant human granulocyte colony-stimulating factor (rhG-CSF). These data demonstrate that administration of SCF in vivo affects extrathymic-origin thymocyte regenerating cells and may influence, directly or indirectly, early prethymic stages of T-cell lymphopoiesis in addition to its known effect on early stages of myelopoiesis and erythropoiesis.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=1285280&dopt=Abstract">Link to Article in PubMed</a>
dc.subjectAnimals
dc.subjectBone Marrow Transplantation
dc.subjectCell Transplantation
dc.subjectFlow Cytometry
dc.subjectHematopoietic Cell Growth Factors
dc.subjectImmunotherapy, Adoptive
dc.subjectMale
dc.subjectRats
dc.subjectRats, Inbred BUF
dc.subjectRegeneration
dc.subjectSpleen
dc.subjectStem Cell Factor
dc.subjectStem Cells
dc.subjectT-Lymphocytes
dc.subjectThymus Gland
dc.subjectWhole-Body Irradiation
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.titleRat stem-cell factor induces splenocytes capable of regenerating the thymus
dc.typeJournal Article
dc.source.journaltitleDevelopmental immunology
dc.source.volume3
dc.source.issue1
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=3310&amp;context=oapubs&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/oapubs/2310
dc.identifier.contextkey2710626
refterms.dateFOA2022-08-23T16:39:38Z
html.description.abstract<p>Cytokine regulation of prethymic T-lymphoid progenitor-cell proliferation and/or differentiation has not been well-defined, although much is known of cytokine regulation of hemopoietic stem- and progenitor-cell development. Here we use a recently identified hemopoietic growth factor, stem-cell factor (SCF) (a form of the c-kit ligand), and a transplant model of thymocyte regeneration to assess the effect of SCF on the in vivo generation of prethymic, thymocyte progenitor-cell activity. We show that recombinant rat SCF (rrSCF164) administered to weanling rats selectively induces an increase in thymocyte progenitor activity in the spleens of treated rats as compared to rats treated with vehicle, polyethylene glycol (PEG)-conjugated rat albumin, or recombinant human granulocyte colony-stimulating factor (rhG-CSF). These data demonstrate that administration of SCF in vivo affects extrathymic-origin thymocyte regenerating cells and may influence, directly or indirectly, early prethymic stages of T-cell lymphopoiesis in addition to its known effect on early stages of myelopoiesis and erythropoiesis.</p>
dc.identifier.submissionpathoapubs/2310
dc.contributor.departmentDepartment of Medicine, Diabetes Division
dc.source.pages35-44


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