TY - JOUR
T1 - Self-segregation of myelin membrane lipids in model membranes
AU - Yurlova, Larisa
AU - Kahya, Nicoletta
AU - Aggarwal, Shweta
AU - Kaiser, Hermann Josef
AU - Chiantia, Salvatore
AU - Bakhti, Mostafa
AU - Pewzner-Jung, Yael
AU - Ben-David, Oshrit
AU - Futerman, Anthony H.
AU - Brügger, Britta
AU - Simons, Mikael
PY - 2011/12/7
Y1 - 2011/12/7
N2 - Rapid conduction of nerve impulses requires coating of axons by myelin sheaths, which are multilamellar, lipid-rich membranes produced by oligodendrocytes in the central nervous system. To act as an insulator, myelin has to form a stable and firm membrane structure. In this study, we have analyzed the biophysical properties of myelin membranes prepared from wild-type mice and from mouse mutants that are unable to form stable myelin. Using C-Laurdan and fluorescence correlation spectroscopy, we find that lipids are tightly organized and highly ordered in myelin isolated from wild-type mice, but not from shiverer and ceramide synthase 2 null mice. Furthermore, only myelin lipids from wild-type mice laterally segregate into physically distinct lipid phases in giant unilamellar vesicles in a process that requires very long chain glycosphingolipids. Taken together, our findings suggest that oligodendrocytes exploit the potential of lipids to self-segregate to generate a highly ordered membrane for electrical insulation of axons.
AB - Rapid conduction of nerve impulses requires coating of axons by myelin sheaths, which are multilamellar, lipid-rich membranes produced by oligodendrocytes in the central nervous system. To act as an insulator, myelin has to form a stable and firm membrane structure. In this study, we have analyzed the biophysical properties of myelin membranes prepared from wild-type mice and from mouse mutants that are unable to form stable myelin. Using C-Laurdan and fluorescence correlation spectroscopy, we find that lipids are tightly organized and highly ordered in myelin isolated from wild-type mice, but not from shiverer and ceramide synthase 2 null mice. Furthermore, only myelin lipids from wild-type mice laterally segregate into physically distinct lipid phases in giant unilamellar vesicles in a process that requires very long chain glycosphingolipids. Taken together, our findings suggest that oligodendrocytes exploit the potential of lipids to self-segregate to generate a highly ordered membrane for electrical insulation of axons.
UR - http://www.scopus.com/inward/record.url?scp=82955169515&partnerID=8YFLogxK
U2 - 10.1016/j.bpj.2011.10.026
DO - 10.1016/j.bpj.2011.10.026
M3 - Article
C2 - 22261060
AN - SCOPUS:82955169515
SN - 0006-3495
VL - 101
SP - 2713
EP - 2720
JO - Biophysical Journal
JF - Biophysical Journal
IS - 11
ER -