Please use this identifier to cite or link to this item: https://observatorio.fm.usp.br/handle/OPI/3032
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dc.contributorSistema FMUSP-HC: Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSP-
dc.contributor.authorLOVISOLO, S. M.-
dc.contributor.authorGARIPPO, A. L.-
dc.contributor.authorGUEDES, F.-
dc.contributor.authorZERBINI, M. C.-
dc.date.accessioned2013-10-11T21:25:47Z-
dc.date.available2013-10-11T21:25:47Z-
dc.date.issued2012-
dc.identifier.citationMODERN PATHOLOGY, v.25, suppl.2, p.470A-470A, 2012-
dc.identifier.issn0893-3952-
dc.identifier.urihttps://observatorio.fm.usp.br/handle/OPI/3032-
dc.description.abstractBackground: CHI is a life-threatening disorder of glucose metabolism of neonates characterized by serum insulin levels unresponsive to blood glucose concentrations. Pancreatic ß-cells regulates insulin secretion through ATP sensitive potassium channels (K ATP channel) formed by sulfonylurea receptor 1 (SUR1) and potassium inward rectifying 6.2 (Kir 6.2) proteins. The ß-cell K ATP channel dependent CHI is classically associated with loss-of-function mutations of these subunits genes. In a previous study [1], no mutations in the Kir6.2 gene and in the 33-37 exons hot spot region of the SUR1 gene were identified in these patients. The aim of this study is to investigate if these subunits were present in the ß-cells of CHI patients. Design: Pancreatic surgical paraffin tissue from 7 neonates (3F/4M, 4-13 mo) with CHI and 8 autopsy pancreatic control tissue (5F/3M, 4-11 mo) were included in the study. Confocal microscopy double-staining immuno fluorescence (insulin/SUR1 and insulin/Kir6.2) was performed in order to detect each protein specifically in the ß-cells. All sections were analyzed under a Zeiss 510 Meta confocal laser scanning microscope (63x). At least 10 different endocrine islets were captured to evaluate the expression of either Kir6.2 or SUR1 (green-488nm) and insulin (red-633nm). Co-expression of insulin/SUR1 and insulin/Kir6.2 was analysed visually (green x red→yellow) and through correlation Pearson’s coefficient(PC) that estimates the goodness of rate association of the two fluorochromes. PC was compared among cases and controls using a nonparametric method (Mann-Whitney). Results: Visual observation clearly revealed the presence of Kir6.2 and SUR1 in a granular cytoplasmic pattern in the ß-cells of cases and controls. Nevertheless, overlap of insulin/Kir6.2 and insulin/SUR1 seemed to be more constant and uniformin controls than in CHI cases, confirmed by the analysis through PC showing a statistically significant decrease in Kir6.2 ( P = 0.0084) and SUR1 ( P = 0.041) in the ß-cells of CHI patients. Conclusions: This is the first demonstration of K ATP channels subunits Kir6.2 and SUR1 in the pancreatic ß-cells of CHI patients using an in situ method. Our results show that both subunits were present in the ß-cells, but are under-expressed in CHI patients compared to controls, adding a new information to this rare condition with a complex pathogenesis.-
dc.language.isoeng-
dc.publisherNATURE PUBLISHING GROUP-
dc.relation.ispartofModern Pathology-
dc.rightsrestrictedAccess-
dc.titleConfocal Microscopy Image Analysis of Pancreatic beta-Cells K-ATP Channel Proteins in Congenital Hyperinsulinism (CHI)-
dc.typeconferenceObject-
dc.rights.holderCopyright NATURE PUBLISHING GROUP-
dc.description.conferencedateMAR 17-23, 2012-
dc.description.conferencelocalVancouver, CANADA-
dc.description.conferencename101st Annual Meeting of the United-States-and-Canadian-Academy-of-Pathology-
dc.subject.wosPathology-
dc.type.categorymeeting abstract-
dc.type.versionpublishedVersion-
hcfmusp.description.beginpage470A-
hcfmusp.description.endpage470A-
hcfmusp.description.issuesuppl 2-
hcfmusp.description.volume25-
hcfmusp.origemWOS-
hcfmusp.origem.idWOS:000299986902469-
hcfmusp.publisher.cityNEW YORK-
hcfmusp.publisher.countryUSA-
hcfmusp.relation.referenceLovisolo SM, 2010, PEDIATR DEVEL PATHOL, V13, P375, DOI 10.2350/08-12-0578.1-
dc.description.indexMEDLINE-
Appears in Collections:

Comunicações em Eventos - FM/MPR
Departamento de Medicina Preventiva - FM/MPR

Comunicações em Eventos - FM/MPT
Departamento de Patologia - FM/MPT

Comunicações em Eventos - HC/IMREA
Instituto de Medicina Física e de Reabilitação - HC/IMREA

Comunicações em Eventos - LIM/14
LIM/14 - Laboratório de Investigação em Patologia Hepática


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