Multiple Sclerosis (MS) is characterized by patchy demyelination within the central nervous system. Remyelination is often incomplete, and the failure of OLGs to remyelinate is at least in part due to OLG programmed cell death (PCD). Caveolin-1 is likely to modulate OLG function and survival. Caveolin-1 forms the structural backbone of caveolae vesicles and has diverse effects on signal transduction, cholesterol transport, cell cycle control, and PCD. By binding to signaling proteins via a region termed the caveolinscaffolding domain (CSD), caveolin-1 regulates (generally inhibits) signal transduction. The CSD binds to conserved regions of signaling molecules, such as the caveolin-binding domain (CBD) of receptor tyrosine kinases. We have previously shown that caveolin-1 expression by Schwann cells increases during development and decreases following nerve transection, which is consistent with findings by others that caveolin-1 expression is differentiation-dependent. Caveolin-1's expression and function in OLGs has not been studied. Insulinlike growth factor I (IGF-I) plays a vital role in OLG development, enhancing myelination and remyelination by OLGs, protecting OLGs from PCD, and preventing demyelination, but the underlying molecular mechanisms are poorly understood. We provide preliminary evidence that caveolin-1 binds to the IGF-I receptor (IGF-IR), contains a putative CBD, and is tyrosine phosphorylated following IGF-IR activation. We have 4 Specific Aims: 1) Analyze IGF-IR signaling and caveolin-1-IGF-IR interactions in OLGs, 2) investigate the effects of caveolin-1 expression and caveolin-1 tyrosine phosphorylation on IGF-IR-mediated signaling, proliferation, differentiation, and susceptibility to PCD, 3) characterize caveolin-1-IGF-IR interactions in OLGs, examining effects on IGFIRmediated signaling, proliferation, differentiation and PCD, and 4) investigate the consequences of caveolin-1-IGF-IR interactions in OLGs in vivo. At the end of these studies, we will better understand caveolin-1's regulation of IGF-IR signaling in OLGs and IGF-IR mediated proliferation, differentiation and neuroprotection of OLGs. Understanding the interplay between the IGF-IR and caveolin-1 and their control of OLG phenotype will provide insight into the molecular basis of myelination by OLGs and, hopefully, guide new treatments for MS.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Scientist Development Award - Research (K02)
Project #
5K02NS042099-03
Application #
6701805
Study Section
NST-2 Subcommittee (NST)
Program Officer
Utz, Ursula
Project Start
2002-01-15
Project End
2004-11-30
Budget Start
2003-12-01
Budget End
2004-11-30
Support Year
3
Fiscal Year
2004
Total Cost
$175,176
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Neurology
Type
Schools of Medicine
DUNS #
073133571
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
Boyanapalli, Madanamohan; Lahoud, Oscar B; Messiaen, Ludwine et al. (2006) Neurofibromin binds to caveolin-1 and regulates ras, FAK, and Akt. Biochem Biophys Res Commun 340:1200-8
Meyer, Amy; van Golen, Cynthia M; Boyanapalli, Madanamohan et al. (2005) Integrin-linked kinase complexes with caveolin-1 in human neuroblastoma cells. Biochemistry 44:932-8
Boyanapalli, Madanamohan; Kottis, Vicky; Lahoud, Oscar et al. (2005) Oligodendrocyte-myelin glycoprotein is present in lipid rafts and caveolin-1-enriched membranes. Glia 52:219-27