TY - JOUR
T1 - N-WASP is required for membrane wrapping and myelination by Schwann cells
AU - Novak, Nurit
AU - Bar, Vered
AU - Sabanay, Helena
AU - Frechter, Shahar
AU - Jaegle, Martine
AU - Snapper, Scott B.
AU - Meijer, Dies
AU - Peles, Elior
N1 - National Institutes of Health [NS50220, 5P01 HL59561]; Dr. Miriam and Sheldon G. Adelson Medical Research Foundation; Israel Science Foundation; Shapell Family Biomedical Research Foundation at the Weizmann Institute; Moskowitz Center for Imaging; European Community [FP7/2007-2013, HEALTH-F2-2008-201535]This work was supported by grants from the National Institutes of Health (NS50220 to E. Peles and 5P01 HL59561 to S.B. Snapper), the Dr. Miriam and Sheldon G. Adelson Medical Research Foundation, the Israel Science Foundation, the Shapell Family Biomedical Research Foundation at the Weizmann Institute, the Moskowitz Center for Imaging, and the European Community's Seventh Framework Program (FP7/2007-2013; HEALTH-F2-2008-201535 to E. Peles and D. Meijer). E. Peles is the Incumbent of the Hanna Hertz Professorial Chair for Multiple Sclerosis and Neuroscience.
PY - 2011/1/24
Y1 - 2011/1/24
N2 - During peripheral nerve myelination, Schwann cells sort larger axons, ensheath them, and eventually wrap their membrane to form the myelin sheath. These processes involve extensive changes in cell shape, but the exact mechanisms involved are still unknown. Neural Wiskott-Aldrich syndrome protein (N-WASP) integrates various extracellular signals to control actin dynamics and cytoskeletal reorganization through activation of the Arp2/3 complex. By generating mice lacking N-WASP in myelinating Schwann cells, we show that N-WASP is crucial for myelination. In N-WASP-deficient nerves, Schwann cells sort and ensheath axons, but most of them fail to myelinate and arrest at the promyelinating stage. Yet, a limited number of Schwann cells form unusually short internodes, containing thin myelin sheaths, with the occasional appearance of myelin misfoldings. These data suggest that regulation of actin filament nucleation in Schwann cells by N-WASP is crucial for membrane wrapping, longitudinal extension, and myelination.
AB - During peripheral nerve myelination, Schwann cells sort larger axons, ensheath them, and eventually wrap their membrane to form the myelin sheath. These processes involve extensive changes in cell shape, but the exact mechanisms involved are still unknown. Neural Wiskott-Aldrich syndrome protein (N-WASP) integrates various extracellular signals to control actin dynamics and cytoskeletal reorganization through activation of the Arp2/3 complex. By generating mice lacking N-WASP in myelinating Schwann cells, we show that N-WASP is crucial for myelination. In N-WASP-deficient nerves, Schwann cells sort and ensheath axons, but most of them fail to myelinate and arrest at the promyelinating stage. Yet, a limited number of Schwann cells form unusually short internodes, containing thin myelin sheaths, with the occasional appearance of myelin misfoldings. These data suggest that regulation of actin filament nucleation in Schwann cells by N-WASP is crucial for membrane wrapping, longitudinal extension, and myelination.
UR - http://www.scopus.com/inward/record.url?scp=78951493203&partnerID=8YFLogxK
U2 - 10.1083/jcb.201010013
DO - 10.1083/jcb.201010013
M3 - مقالة
SN - 0021-9525
VL - 192
SP - 243
EP - 250
JO - Journal of Cell Biology
JF - Journal of Cell Biology
IS - 2
ER -