TY - JOUR
T1 - Cholesterol access in cellular membranes controls Hedgehog signaling
AU - Radhakrishnan, Arun
AU - Rohatgi, Rajat
AU - Siebold, Christian
N1 - Funding Information:
We acknowledge G. Pusapati for help with the figures and comments on the manuscript. C.S. was supported by grants from Cancer Research UK (C20724/A26752) and the European Research Council (647278), R.R. by grants from the National Institutes of Health (GM118082 and GM106078), and A.R. by grants from the NIH (HL20948), Welch Foundation (I-1793) and Leducq Foundation (19CVD04).
Publisher Copyright:
© 2020, Springer Nature America, Inc.
PY - 2020/12
Y1 - 2020/12
N2 - The Hedgehog (Hh) signaling pathway coordinates cell–cell communication in development and regeneration. Defects in this pathway underlie diseases ranging from birth defects to cancer. Hh signals are transmitted across the plasma membrane by two proteins, Patched 1 (PTCH1) and Smoothened (SMO). PTCH1, a transporter-like tumor-suppressor protein, binds to Hh ligands, but SMO, a G-protein-coupled-receptor family oncoprotein, transmits the Hh signal across the membrane. Recent structural, biochemical and cell-biological studies have converged at the surprising model that a specific pool of plasma membrane cholesterol, termed accessible cholesterol, functions as a second messenger that conveys the signal between PTCH1 and SMO. Beyond solving a central puzzle in Hh signaling, these studies are revealing new principles in membrane biology: how proteins respond to and remodel cholesterol accessibility in membranes and how the cholesterol composition of organelle membranes is used to regulate protein function.
AB - The Hedgehog (Hh) signaling pathway coordinates cell–cell communication in development and regeneration. Defects in this pathway underlie diseases ranging from birth defects to cancer. Hh signals are transmitted across the plasma membrane by two proteins, Patched 1 (PTCH1) and Smoothened (SMO). PTCH1, a transporter-like tumor-suppressor protein, binds to Hh ligands, but SMO, a G-protein-coupled-receptor family oncoprotein, transmits the Hh signal across the membrane. Recent structural, biochemical and cell-biological studies have converged at the surprising model that a specific pool of plasma membrane cholesterol, termed accessible cholesterol, functions as a second messenger that conveys the signal between PTCH1 and SMO. Beyond solving a central puzzle in Hh signaling, these studies are revealing new principles in membrane biology: how proteins respond to and remodel cholesterol accessibility in membranes and how the cholesterol composition of organelle membranes is used to regulate protein function.
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U2 - 10.1038/s41589-020-00678-2
DO - 10.1038/s41589-020-00678-2
M3 - Review article
C2 - 33199907
AN - SCOPUS:85096077627
SN - 1552-4450
VL - 16
SP - 1303
EP - 1313
JO - Nature Chemical Biology
JF - Nature Chemical Biology
IS - 12
ER -