Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/11536
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dc.contributor.authorSharma, Varun-
dc.contributor.authorLing, Tina W-
dc.contributor.authorRewell, Sarah S-
dc.contributor.authorHare, David L-
dc.contributor.authorHowells, David William-
dc.contributor.authorKourakis, Angela-
dc.contributor.authorWookey, Peter J-
dc.date.accessioned2015-05-16T01:09:00Z
dc.date.available2015-05-16T01:09:00Z
dc.date.issued2012-07-18en
dc.identifier.citationJournal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism 2012; 32(11): 2055-65en
dc.identifier.govdoc22805872en
dc.identifier.otherPUBMEDen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/11536en
dc.description.abstractIn a rat model of stroke, the spatio-temporal distribution of α-smooth muscle actin-positive, (αSMA+) cells was investigated in the infarcted hemisphere (ipsilateral) and compared with the contralateral hemisphere. At day 3 postischemia, αSMA+ cells were concentrated in two main loci within the ipsilateral hemisphere (Area A) in the medial corpus callosum and (Area B) midway through the striatum adjacent to the lateral ventricle. By day 7 and further by day 14, fewer αSMA+ cells remained in Areas A and B but a steady increase in the peri-infarct was observed. αSMA+ cells also expressed glial acidic fibrillary protein [GFAP: αSMA+/GFAP+ (29%); αSMA+/GFAP- (71%) phenotypes] and feline leukemia virus C receptor 2 (FLVCR2), but not ED1(microglia) and established markers of pericytes normally located in vascular wall. αSMA+ cells were also located close to the subventricular zones (SVZ) adjacent to Areas A and B. In conclusion, αSMA+ cells have been identified in a spatial and temporal sequence from the SVZ, at intermediate loci and in the vicinity of the peri-infarct. It is hypothesized that novel populations of αSMA+ precursors of pericytes are born on the SVZ, migrate into the peri-infarct region and are incorporated into new vessels of the peri-infarct regions.en
dc.language.isoenen
dc.subject.otherActins.metabolismen
dc.subject.otherAnimalsen
dc.subject.otherBiological Markersen
dc.subject.otherBrain Ischemia.pathologyen
dc.subject.otherEctodysplasins.metabolismen
dc.subject.otherFluorescent Antibody Techniqueen
dc.subject.otherFunctional Laterality.physiologyen
dc.subject.otherImmunohistochemistryen
dc.subject.otherInfarction, Middle Cerebral Artery.pathologyen
dc.subject.otherKi-67 Antigen.metabolismen
dc.subject.otherMacrophages.metabolismen
dc.subject.otherMaleen
dc.subject.otherMicroglia.metabolismen
dc.subject.otherMicroscopy, Confocalen
dc.subject.otherMyocytes, Smooth Muscle.metabolism.pathology.ultrastructureen
dc.subject.otherParaffin Embeddingen
dc.subject.otherRatsen
dc.subject.otherRats, Inbred SHRen
dc.subject.otherStroke.pathologyen
dc.titleA novel population of ?�-smooth muscle actin-positive cells activated in a rat model of stroke: an analysis of the spatio-temporal distribution in response to ischemia.en
dc.typeJournal Articleen
dc.identifier.journaltitleJournal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolismen
dc.identifier.affiliationCardiology Department, Austin Health, Heidelberg, Victoria, Australiaen
dc.identifier.doi10.1038/jcbfm.2012.107en
dc.description.pages2055-65en
dc.identifier.orcid0000-0001-9554-6556-
dc.identifier.pubmedid22805872-
dc.type.austinJournal Articleen
local.name.researcherHare, David L
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.openairetypeJournal Article-
item.grantfulltextnone-
item.languageiso639-1en-
crisitem.author.deptCardiology-
crisitem.author.deptMedicine (University of Melbourne)-
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