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Expression of neutrophil gelatinase-associated lipocalin (NGAL) in the gut in Crohn's disease.
Thorsvik, Silje; Bakke, Ingunn; van Beelen Granlund, Atle; Røyset, Elin Synnøve; Damås, Jan Kristian; Østvik, Ann Elisabet; Sandvik, Arne Kristian.
Afiliação
  • Thorsvik S; Centre of Molecular Inflammation Research, NTNU, Norwegian University of Science and Technology, Trondheim, Norway.
  • Bakke I; Department of Clinical and Molecular Medicine, NTNU, Norwegian University of Science and Technology, 7489, Trondheim, Norway.
  • van Beelen Granlund A; Department of Gastroenterology, St Olav's University Hospital, Trondheim, Norway.
  • Røyset ES; Department of Clinical and Molecular Medicine, NTNU, Norwegian University of Science and Technology, 7489, Trondheim, Norway.
  • Damås JK; Clinic of Medicine, St Olav's University Hospital, Trondheim, Norway.
  • Østvik AE; Centre of Molecular Inflammation Research, NTNU, Norwegian University of Science and Technology, Trondheim, Norway.
  • Sandvik AK; Department of Clinical and Molecular Medicine, NTNU, Norwegian University of Science and Technology, 7489, Trondheim, Norway.
Cell Tissue Res ; 374(2): 339-348, 2018 Nov.
Article em En | MEDLINE | ID: mdl-29869714
ABSTRACT
The antimicrobial glycoprotein neutrophil gelatinase-associated lipocalin (NGAL) is strongly expressed in several infectious, inflammatory and malignant disorders, among these inflammatory bowel disease (IBD). Fecal and serum NGAL is elevated during active IBD and we have recently shown that fecal NGAL is a novel biomarker for IBD with a test performance comparable to the established fecal biomarker calprotectin. This study examines expression of NGAL in the healthy gut and in Crohn's disease (CD), with emphasis on the previously unexplored small intestine. Pinch biopsies were taken from active and inactive CD in jejunum, ileum and colon and from the same sites in healthy controls. Microarray gene expression showed that the NGAL gene, LCN2, was the second most upregulated among 1820 differentially expressed genes in terminal ileum comparing active CD and controls (FC 5.86, p = 0.027). Based on immunohistochemistry and in situ hybridization findings, this upregulation most likely represented increased expression in epithelial cells. Double immunofluorescence showed NGAL expression in 49% (range 19-70) of Paneth cells (PCs) in control ileum with no change during inflammation. In healthy jejunum, the NGAL expression in PCs was weak to none but markedly increased during active CD. We further found NGAL also in metaplastic PCs in colon. Finally, we show for the first time that NGAL is expressed in enteroendocrine cells in small intestine as well as in colon.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Crohn / Sistema Digestório / Lipocalina-2 Tipo de estudo: Risk_factors_studies Limite: Adult / Humans / Middle aged Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Crohn / Sistema Digestório / Lipocalina-2 Tipo de estudo: Risk_factors_studies Limite: Adult / Humans / Middle aged Idioma: En Ano de publicação: 2018 Tipo de documento: Article