TY - JOUR
T1 - Early Functional Impairment of Sensory-Motor Connectivity in a Mouse Model of Spinal Muscular Atrophy
AU - Mentis, George Z.
AU - Blivis, Dvir
AU - Liu, Wenfang
AU - Drobac, Estelle
AU - Crowder, Melissa E.
AU - Kong, Lingling
AU - Alvarez, Francisco J.
AU - Sumner, Charlotte J.
AU - O'Donovan, Michael J.
N1 - Funding Information:
We are grateful to Drs. T.M. Jessell, C.E. Henderson, S. Przedborski, L. Pellizzoni, N.A. Shneider, and K. Fischbeck for comments on the manuscript and for the generous support of Dr. K. Fischbeck. The technical assistance of the late Ms. A.A. Taye (genotyping) and Mrs. J. Sisco (muscle spindle staining) is also appreciated. Thanks to Dr. D. Ladle for assistance in muscle dissection. The work was supported by the NINDS Intramural Program and the SMA Foundation (G.Z.M.). C.J.S. was supported by an NINDS grant (R01NS062869) and Howard Hughes Medical Institute Physician Scientist Award.
PY - 2011/2/10
Y1 - 2011/2/10
N2 - To define alterations of neuronal connectivity that occur during motor neuron degeneration, we characterized the function and structure of spinal circuitry in spinal muscular atrophy (SMA) model mice. SMA motor neurons show reduced proprioceptive reflexes that correlate with decreased number and function of synapses on motor neuron somata and proximal dendrites. These abnormalities occur at an early stage of disease in motor neurons innervating proximal hindlimb muscles and medial motor neurons innervating axial muscles, but only at end-stage disease in motor neurons innervating distal hindlimb muscles. Motor neuron loss follows afferent synapse loss with the same temporal and topographical pattern. Trichostatin A, which improves motor behavior and survival of SMA mice, partially restores spinal reflexes, illustrating the reversibility of these synaptic defects. Deafferentation of motor neurons is an early event in SMA and may be a primary cause of motor dysfunction that is amenable to therapeutic intervention.
AB - To define alterations of neuronal connectivity that occur during motor neuron degeneration, we characterized the function and structure of spinal circuitry in spinal muscular atrophy (SMA) model mice. SMA motor neurons show reduced proprioceptive reflexes that correlate with decreased number and function of synapses on motor neuron somata and proximal dendrites. These abnormalities occur at an early stage of disease in motor neurons innervating proximal hindlimb muscles and medial motor neurons innervating axial muscles, but only at end-stage disease in motor neurons innervating distal hindlimb muscles. Motor neuron loss follows afferent synapse loss with the same temporal and topographical pattern. Trichostatin A, which improves motor behavior and survival of SMA mice, partially restores spinal reflexes, illustrating the reversibility of these synaptic defects. Deafferentation of motor neurons is an early event in SMA and may be a primary cause of motor dysfunction that is amenable to therapeutic intervention.
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U2 - 10.1016/j.neuron.2010.12.032
DO - 10.1016/j.neuron.2010.12.032
M3 - Article
C2 - 21315257
AN - SCOPUS:79551663958
SN - 0896-6273
VL - 69
SP - 453
EP - 467
JO - Neuron
JF - Neuron
IS - 3
ER -