Schwann cells and oligodendrocytes produce myelin sheaths of widely varying
sizes. How these cells determine the size of myelin sheath for a particula
r axon is incompletely understood. Axonal diameter has long been suspected
to be a signal in this process. We have analyzed myelin sheath thickness in
L5 lumbar root and spinal cord white matter of a series of mouse mutants w
ith diminished axonal calibers resulting from a deficiency of neurofilament
s (NFs). In the PNS, average axonal diameters were reduced by 20-37% in the
NF mutants. Remarkably, the average myelin sheath thickness remained uncha
nged from control values, and regression analysis showed sheaths abnormally
thick for a given size of axon. These data show that a genetically induced
reduction in axonal caliber does not cause a reduction in myelin sheath th
ickness in PNS and indicate that Schwann cells read some intrinsic signal o
n axons that can be uncoupled from axonal diameter. Interestingly, myelin s
heaths in the spinal cord of these animals were not abnormally thick, argui
ng that axonal diameter may contribute directly to the regulation of myelin
ation in the CNS and that oligodendrocytes and Schwann cells use different
cues to set myelin sheath thickness. J. Neurosci. Res. 65:493-499, 2001. (C
) 2001 Wiley-Liss, Inc.