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Increased GPNMB, phospho-ERK1/2, and MMP-9 in cystic fibrosis in association with reduced arylsulfatase B.
Bhattacharyya, Sumit; Feferman, Leo; Sharma, Girish; Tobacman, Joanne K.
Afiliação
  • Bhattacharyya S; Department of Medicine, College of Medicine, University of Illinois at Chicago, Chicago, IL, USA; Jesse Brown VAMC, Chicago, IL, 60612, USA.
  • Feferman L; Department of Medicine, College of Medicine, University of Illinois at Chicago, Chicago, IL, USA; Jesse Brown VAMC, Chicago, IL, 60612, USA.
  • Sharma G; Department of Pediatrics, Rush University Medical Center, Chicago, IL 60612, USA.
  • Tobacman JK; Department of Medicine, College of Medicine, University of Illinois at Chicago, Chicago, IL, USA; Jesse Brown VAMC, Chicago, IL, 60612, USA. Electronic address: jkt@uic.edu.
Mol Genet Metab ; 124(2): 168-175, 2018 06.
Article em En | MEDLINE | ID: mdl-29703589
BACKGROUND: GPNMB was increased in a CF gene array and in Arylsulfatase B (ARSB; N-acetylgalactosamine-4-sulfatase)-null mice, consistent with previous reports that ARSB is reduced in cystic fibrosis (CF). Implications of GPNMB increase in CF are unknown. METHODS: GPNMB levels were determined in serum and circulating leukocytes from CF patients and healthy controls. GPNMB binding with ß-1 integrin and measurements of phospho-ERK1/2 and MMP-9 in CFTR-uncorrected, CFTR-corrected, and normal human bronchial epithelial cells (BEC) were determined, following ARSB and GPNMB knockdown, and treatment with RGD peptide, and ERK phosphorylation inhibitor. RESULTS: GPNMB was markedly increased in CF patients compared to controls (p < 0.0001, unpaired t-test, two-tailed). Silencing GPNMB, treatment with excess RGD peptide, and treatment with ERK phosphorylation inhibitor blocked ARSB silencing-induced increases in MMP-9 in the normal BEC. CONCLUSIONS: Findings suggest that decline in ARSB activity caused by decline in CFTR function leads to increased GPNMB, which may contribute to organ dysfunction in CF by increased MMP-9 expression.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Glicoproteínas de Membrana / Biomarcadores / Proteína Quinase 1 Ativada por Mitógeno / N-Acetilgalactosamina-4-Sulfatase / Metaloproteinase 9 da Matriz / Fibrose Cística / Proteína Quinase 3 Ativada por Mitógeno Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Revista: Mol Genet Metab Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Glicoproteínas de Membrana / Biomarcadores / Proteína Quinase 1 Ativada por Mitógeno / N-Acetilgalactosamina-4-Sulfatase / Metaloproteinase 9 da Matriz / Fibrose Cística / Proteína Quinase 3 Ativada por Mitógeno Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Revista: Mol Genet Metab Ano de publicação: 2018 Tipo de documento: Article