The ABCA1 cholesterol transporter associates with one of two distinct dystrophin-based scaffolds in Schwann cells

被引:17
作者
Albrecht, Douglas E. [1 ]
Sherman, Dlalne L. [2 ]
Brophy, Peter J. [2 ]
Froehner, Stanley C. [1 ]
机构
[1] Univ Washington, Dept Physiol & Biophys, Seattle, WA 98195 USA
[2] Univ Edinburgh, Neurosci Res Ctr, Edinburgh, Midlothian, Scotland
关键词
myelination; Schwann cell; dystrophin; syntrophin; ABCA1;
D O I
10.1002/glia.20636
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Cytoskeletal scaffolding complexes help organize specialized membrane domains with unique functions on the surface of cells. In this study, we define the scaffolding potential of the Schwarm cell dystrophin glycoprotein complex (DGC) by establishing the presence of four syntrophin isoforms, (alpha 1, beta 1, beta 2, and gamma 2), and one dystrobrevin isoform, (alpha-dystrobrevin-1), in the abaxonal membrane. Furthermore, we demonstrate the existence of two separate DGCs in Schwarm cells that divide the abaxonal membrane into spatially distinct domains, the DRP2/periaxin rich plaques and the Cajal bands that contain Dp116, utrophin, alpha-dystrobrevin-1 and four syntrophin isoforms. Finally, we show that the two different DGCs can scaffold unique accessory molecules in distinct areas of the Schwarm cell membrane. Specifically, the cholesterol transporter ABCA1, associates with the Dp116/syntrophin complex in Cajal bands and is excluded from the DRP2/periaxin rich plaques. (C) 2008 Wiley-Liss, Inc.
引用
收藏
页码:611 / 618
页数:8
相关论文
共 60 条
[1]
Absence of α-syntrophin leads to structurally aberrant neuromuscular synapses deficient in utrophin [J].
Adams, ME ;
Kramarcy, N ;
Krall, SP ;
Rossi, SG ;
Rotundo, RL ;
Sealock, R ;
Froehner, SC .
JOURNAL OF CELL BIOLOGY, 2000, 150 (06) :1385-1397
[2]
Structural abnormalities at neuromuscular synapses lacking multiple syntrophin isoforms [J].
Adams, ME ;
Kramarcy, N ;
Fukuda, T ;
Engel, AG ;
Sealock, R ;
Froehner, SC .
JOURNAL OF NEUROSCIENCE, 2004, 24 (46) :10302-10309
[3]
2 FORMS OF MOUSE SYNTROPHIN, A 58-KD DYSTROPHIN-ASSOCIATED PROTEIN, DIFFER IN PRIMARY STRUCTURE AND TISSUE DISTRIBUTION [J].
ADAMS, ME ;
BUTLER, MH ;
DWYER, TM ;
PETERS, MF ;
MURNANE, AA ;
FROEHNER, SC .
NEURON, 1993, 11 (03) :531-540
[4]
In vivo requirement of the α-syntrophin PDZ domain for the sarcolemmal localization of nNOS and aquaporin-4 [J].
Adams, ME ;
Mueller, HA ;
Froehner, SC .
JOURNAL OF CELL BIOLOGY, 2001, 155 (01) :113-122
[5]
DAMAGE, a novel α-dystrobrevin-associated MAGE protein in dystrophin complexes [J].
Albrecht, DE ;
Froehner, SC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (08) :7014-7023
[6]
Syntrophins and dystrobrevins: Defining the dystrophin scaffold at synapses [J].
Albrecht, DE ;
Froehner, SC .
NEUROSIGNALS, 2002, 11 (03) :123-129
[7]
γ-Syntrophin scaffolding is spatially and functionally distinct from that of the α/β syntrophins [J].
Alessi, Amy ;
Bragg, April D. ;
Percival, Justin M. ;
Yoo, Jean ;
Albrecht, Douglas E. ;
Froehner, Stanley C. ;
Adams, Marvin E. .
EXPERIMENTAL CELL RESEARCH, 2006, 312 (16) :3084-3095
[8]
Alpha syntrophin deletion removes the perivascular but not the endothelial pool of aquaporin-4 at the blood-brain barrier and delays the development of brain edema in an experimental model of acute hyponatremia [J].
Amiry-Moghaddam, M ;
Xue, R ;
Haug, FM ;
Neely, JD ;
Bhardwaj, A ;
Agre, P ;
Adams, ME ;
Froehner, SC ;
Mori, S ;
Ottersen, OP .
FASEB JOURNAL, 2004, 18 (01) :542-+
[9]
Dysbindin, a novel coiled-coil-containing protein that interacts with the dystrobrevins in muscle and brain [J].
Benson, MA ;
Newey, SE ;
Martin-Rendon, E ;
Hawkes, R ;
Blake, DJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (26) :24232-24241
[10]
DIFFERENT DISTRIBUTIONS OF DYSTROPHIN AND RELATED PROTEINS AT NERVE MUSCLE JUNCTIONS [J].
BEWICK, GS ;
NICHOLSON, LVB ;
YOUNG, C ;
ODONNELL, E ;
SLATER, CR .
NEUROREPORT, 1992, 3 (10) :857-860