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Cholesterol accessibility at the ciliary membrane controls hedgehog signaling.
Kinnebrew, Maia; Iverson, Ellen J; Patel, Bhaven B; Pusapati, Ganesh V; Kong, Jennifer H; Johnson, Kristen A; Luchetti, Giovanni; Eckert, Kaitlyn M; McDonald, Jeffrey G; Covey, Douglas F; Siebold, Christian; Radhakrishnan, Arun; Rohatgi, Rajat.
Afiliación
  • Kinnebrew M; Department of Biochemistry, Stanford University School of Medicine, Stanford, United States.
  • Iverson EJ; Department of Biochemistry, Stanford University School of Medicine, Stanford, United States.
  • Patel BB; Department of Biochemistry, Stanford University School of Medicine, Stanford, United States.
  • Pusapati GV; Department of Biochemistry, Stanford University School of Medicine, Stanford, United States.
  • Kong JH; Department of Biochemistry, Stanford University School of Medicine, Stanford, United States.
  • Johnson KA; Department of Molecular Genetics, University of Texas Southwestern Medical Center, Dallas, United States.
  • Luchetti G; Department of Biochemistry, Stanford University School of Medicine, Stanford, United States.
  • Eckert KM; Center for Human Nutrition, University of Texas Southwestern Medical Center, Dallas, United States.
  • McDonald JG; Department of Molecular Genetics, University of Texas Southwestern Medical Center, Dallas, United States.
  • Covey DF; Center for Human Nutrition, University of Texas Southwestern Medical Center, Dallas, United States.
  • Siebold C; Taylor Family Institute for Innovative Psychiatric Research, Washington University School of Medicine, St. Louis, United States.
  • Radhakrishnan A; Department of Developmental Biology, Washington University School of Medicine, St. Louis, United States.
  • Rohatgi R; Division of Structural Biology, Wellcome Centre for Human Genetics, University of Oxford, Oxford, United Kingdom.
Elife ; 82019 10 30.
Article en En | MEDLINE | ID: mdl-31657721
ABSTRACT
Previously we proposed that transmission of the hedgehog signal across the plasma membrane by Smoothened is triggered by its interaction with cholesterol (Luchetti et al., 2016). But how is cholesterol, an abundant lipid, regulated tightly enough to control a signaling system that can cause birth defects and cancer? Using toxin-based sensors that distinguish between distinct pools of cholesterol, we find that Smoothened activation and Hedgehog signaling are driven by a biochemically-defined, small fraction of membrane cholesterol, termed accessible cholesterol. Increasing cholesterol accessibility by depletion of sphingomyelin, which sequesters cholesterol in complexes, amplifies Hedgehog signaling. Hedgehog ligands increase cholesterol accessibility in the membrane of the primary cilium by inactivating the transporter-like protein Patched 1. Trapping this accessible cholesterol blocks Hedgehog signal transmission across the membrane. Our work shows that the organization of cholesterol in the ciliary membrane can be modified by extracellular ligands to control the activity of cilia-localized signaling proteins.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Transducción de Señal / Colesterol / Cilios / Proteínas Hedgehog Límite: Animals / Humans Idioma: En Revista: Elife Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Transducción de Señal / Colesterol / Cilios / Proteínas Hedgehog Límite: Animals / Humans Idioma: En Revista: Elife Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos