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Blood ; 120(25): 5032-40, 2012 Dec 13.
Artigo em Inglês | MEDLINE | ID: mdl-23002115

RESUMO

Patients with platelet α or dense δ-granule defects have bleeding problems. Although several proteins are known to be required for δ-granule development, less is known about α-granule biogenesis. Our previous work showed that the BEACH protein NBEAL2 and the Sec1/Munc18 protein VPS33B are required for α-granule biogenesis. Using a yeast two-hybrid screen, mass spectrometry, coimmunoprecipitation, and bioinformatics studies, we identified VPS16B as a VPS33B-binding protein. Immunoblotting confirmed VPS16B expression in various human tissues and cells including megakaryocytes and platelets, and also in megakaryocytic Dami cells. Characterization of platelets from a patient with arthrogryposis, renal dysfunction, and cholestasis (ARC) syndrome containing mutations in C14orf133 encoding VPS16B revealed pale-appearing platelets in blood films and electron microscopy revealed a complete absence of α-granules, whereas δ-granules were observed. Soluble and membrane-bound α-granule proteins were reduced or undetectable, suggesting that both releasable and membrane-bound α-granule constituents were absent. Immunofluorescence microscopy of Dami cells stably expressing GFP-VPS16B revealed that similar to VPS33B, GFP-VPS16B colocalized with markers of the trans-Golgi network, late endosomes and α-granules. We conclude that VPS16B, similar to its binding partner VPS33B, is essential for megakaryocyte and platelet α-granule biogenesis.


Assuntos
Plaquetas/patologia , Proteínas de Transporte/metabolismo , Megacariócitos/patologia , Vesículas Secretórias/metabolismo , Proteínas de Transporte Vesicular/metabolismo , Artrogripose/metabolismo , Artrogripose/patologia , Plaquetas/metabolismo , Proteínas de Transporte/análise , Proteínas de Transporte/genética , Linhagem Celular , Colestase/metabolismo , Colestase/patologia , Cromossomos Humanos Par 14/genética , Cromossomos Humanos Par 14/metabolismo , Códon sem Sentido , Feminino , Complexo de Golgi/ultraestrutura , Células HEK293 , Humanos , Recém-Nascido , Megacariócitos/metabolismo , Fases de Leitura Aberta , Filogenia , Ligação Proteica , Insuficiência Renal/metabolismo , Insuficiência Renal/patologia , Vesículas Secretórias/patologia
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