A Missense Point Mutation in Nerve Growth Factor (NGFR100W) Results in Selective Peripheral Sensory Neuropathy

Yang, W.; Sung, K.; Xu, W.; Rodriguez, M. J.; Wu, A.; Santos, S. A.; Fang, S.; Uber, R. K.; Dong, S. X.; Guillory, B. C.; Orain, X.; Raus, J.; Jolivalt, C.; Calcutt, N.; Ding, J.; Rissman, R. A.; Wu, C.

doi:10.1101/784660

bioRxiv · 10.1101/784660

A Missense Point Mutation in Nerve Growth Factor (NGFR100W) Results in Selective Peripheral Sensory Neuropathy

Yang, W.·Sung, K.·Xu, W.·Rodriguez, M. J.·Wu, A.·Santos, S. A.·Fang, S.·Uber, R. K.·Dong, S. X.·Guillory, B. C.·Orain, X.·Raus, J.·Jolivalt, C.·Calcutt, N.·Ding, J.·Rissman, R. A.·Wu, C.

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Abstract

A missense point mutation in nerve growth factor (NGFR100W) is associated with hereditary sensory autonomic neuropathy V (HSAN V), originally discovered in a Swedish family. These patients develop severe loss of perception to deep pain but with apparently normal cognitive functions. To better understand the disease mechanism, we have generated the first NGFR100W knockin mouse model of HSAN V. Mice homozygous for the NGFR100W mutation (NGFfln/fln) showed significant structural deficits in intra-epidermal nerve fibers (IENFs) at birth. These mice had a total loss of pain perception at [~]2 months of age and they often failed to survive to full adulthood. Heterozygous mice (NGF+/fln) developed a progressive degeneration of small sensory fibers both behaviorally and functionally: they showed a progressive loss of IENFs starting at the age of 9 months accompanied with progressive loss of perception to painful stimuli such as noxious temperature. Quantitative analysis of lumbar 4/5 dorsal root ganglia (DRG) revealed a significant reduction in small size neurons positive for calcitonin gene-related peptide, while analysis of sciatic nerve fibers revealed the mutant NGF+/fln mice had no reduction in myelinated nerve fibers. Significantly, the amount of NGF secreted from fibroblasts were reduced in heterozygous and homozygous mice compared to their wild-type littermates. Interestingly, NGF+/fln showed no apparent structural alteration in the brain: neither the anterior cingulate cortex nor the medial septum including NGF-dependent basal forebrain cholinergic neurons. Accordingly, these animals did not develop appreciable deficits in tests for central nervous system function. Our study provides novel insights into the selective impact of NGFR100W mutation on the development and function of the peripheral sensory system.

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Yang, W., Sung, K., Xu, W., Rodriguez, M. J., Wu, A., Santos, S. A., Fang, S., Uber, R. K., Dong, S. X., Guillory, B. C., Orain, X., Raus, J., Jolivalt, C., Calcutt, N., Ding, J., Rissman, R. A., Wu, C.. 2019-09-27. A Missense Point Mutation in Nerve Growth Factor (NGFR100W) Results in Selective Peripheral Sensory Neuropathy. https://doi.org/10.1101/784660

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