TY - JOUR
T1 - An essential role of MAG in mediating axon-myelin attachment in Charcot-Marie-Tooth 1A disease
AU - Kinter, Jochen
AU - Lazzati, Thomas
AU - Schmid, Daniela
AU - Zeis, Thomas
AU - Erne, Beat
AU - Lützelschwab, Roland
AU - Steck, Andreas J.
AU - Pareyson, Davide
AU - Peles, Elior
AU - Schaeren-Wiemers, Nicole
N1 - Swiss National Science Foundation [3100A 0-112583]; NIH (NINDS) [NS50220]Thanks goes to Dr. Bettina Geidl-Fluck (Neurobiology, Department of Biomedicine, Basel, Switzerland) for her experimental contribution, to Dr. Alphonse Probst (Neuropathology, University Hospital Basel, Switzerland) for providing control autopsies, to Dr. Care Huxley (Division of Biomedical Sciences, Imperial College School of Science, London, UK) for providing the PMP22 overexpressing mice, to Dr. Klaus Armin Nave (MPI Gottingen, Germany) for providing the MAG knockout mice, to Dr. Leda Dimou (Institute for Physiology, Ludwig-Maximilians-Universitat, Munich, Germany) for providing some MAG knockout tissues, Dr. Ueli Certa (Molecular Toxicology, Pharmaceutical Divison, F. Hoffmann-La-Roche AG, Basel, Switzerland) for access to the microarray facility and technical support, and to Dr. Hans-Rudolf Brenner and Dr. Nadine Schmidt (Institute for Physiology, University of Basel, Switzerland) for the analysis of the neuromuscular junction. This work was supported by the Swiss National Science Foundation (to NSW 3100A 0-112583) and the NIH (NINDS grant NS50220 to EP).
PY - 2013/1
Y1 - 2013/1
N2 - Charcot-Marie-Tooth disease type 1A (CMT1A) is a hereditary demyelinating peripheral neuropathy caused by the duplication of the PMP22 gene. Demyelination precedes the occurrence of clinical symptoms that correlate with axonal degeneration. It was postulated that a disturbed axon-glia interface contributes to altered myelination consequently leading to axonal degeneration. In this study, we examined the expression of MAG and Necl4, two critical adhesion molecules that are present at the axon-glia interface, in sural nerve biopsies of CMT1A patients and in peripheral nerves of mice overexpressing human PMP22, an animal model for CMT1A. We show an increase in the expression of MAG and a strong decrease of Necl4 in biopsies of CMT1A patients as well as in CMT1A mice. Expression analysis revealed that MAG is strongly upregulated during peripheral nerve maturation, whereas Necl4 expression remains very low. Ablating MAG in CMT1A mice results in separation of axons from their myelin sheath. Our data show that MAG is important for axon-glia contact in a model for CMT1A, and suggest that its increased expression in CMT1A disease has a compensatory role in the pathology of the disease. Thus, we demonstrate that MAG together with other adhesion molecules such as Necl4 is important in sustaining axonal integrity.
AB - Charcot-Marie-Tooth disease type 1A (CMT1A) is a hereditary demyelinating peripheral neuropathy caused by the duplication of the PMP22 gene. Demyelination precedes the occurrence of clinical symptoms that correlate with axonal degeneration. It was postulated that a disturbed axon-glia interface contributes to altered myelination consequently leading to axonal degeneration. In this study, we examined the expression of MAG and Necl4, two critical adhesion molecules that are present at the axon-glia interface, in sural nerve biopsies of CMT1A patients and in peripheral nerves of mice overexpressing human PMP22, an animal model for CMT1A. We show an increase in the expression of MAG and a strong decrease of Necl4 in biopsies of CMT1A patients as well as in CMT1A mice. Expression analysis revealed that MAG is strongly upregulated during peripheral nerve maturation, whereas Necl4 expression remains very low. Ablating MAG in CMT1A mice results in separation of axons from their myelin sheath. Our data show that MAG is important for axon-glia contact in a model for CMT1A, and suggest that its increased expression in CMT1A disease has a compensatory role in the pathology of the disease. Thus, we demonstrate that MAG together with other adhesion molecules such as Necl4 is important in sustaining axonal integrity.
UR - http://www.scopus.com/inward/record.url?scp=84867136836&partnerID=8YFLogxK
U2 - https://doi.org/10.1016/j.nbd.2012.08.009
DO - https://doi.org/10.1016/j.nbd.2012.08.009
M3 - مقالة
SN - 0969-9961
VL - 49
SP - 221
EP - 231
JO - Neurobiology of Disease
JF - Neurobiology of Disease
IS - 1
ER -