2024-03-28T21:52:51Zhttp://repisalud.isciii.es/oai/requestoai:repisalud.isciii.es:20.500.12105/96672023-10-09T11:58:06Zcom_20.500.12105_2102com_20.500.12105_2052com_20.500.12105_2051col_20.500.12105_2103
00925njm 22002777a 4500
dc
Franco, María Luisa
author
Melero, Cristina
author
Sarasola, Esther
author
Acebo, Paloma
author
Luque, Alfonso
author
Calatayud-Baselga, Isabel
author
García-Barcina, María
author
Vilar, Marçal
author
2016-10-07
Congenital insensitivity to pain with anhidrosis (CIPA) is a rare autosomal recessive disorder characterized by insensitivity to noxious stimuli and variable intellectual disability (ID) due to mutations in the NTRK1 gene encoding the NGF receptor TrkA. To get an insight in the effect of NTRK1 mutations in the cognitive phenotype we biochemically characterized three TrkA mutations identified in children diagnosed of CIPA with variable ID. These mutations are located in different domains of the protein; L213P in the extracellular domain, Δ736 in the kinase domain, and C300stop in the extracellular domain, a new mutation causing CIPA diagnosed in a Spanish teenager. We found that TrkA mutations induce misfolding, retention in the endoplasmic reticulum (ER), and aggregation in a mutation-dependent manner. The distinct mutations are degraded with a different kinetics by different ER quality control mechanisms; although C300stop is rapidly disposed by autophagy, Δ736 degradation is sensitive to the proteasome and to autophagy inhibitors, and L213P is a long-lived protein refractory to degradation. In addition L213P enhances the formation of autophagic vesicles triggering an increase in the autophagic flux with deleterious consequences. Mouse cortical neurons expressing L213P showed the accumulation of LC3-GFP positive puncta and dystrophic neurites. Our data suggest that TrkA misfolding and aggregation induced by some CIPA mutations disrupt the autophagy homeostasis causing neurodegeneration. We propose that distinct disease-causing mutations of TrkA generate different levels of cell toxicity, which may provide an explanation of the variable intellectual disability observed in CIPA patients.
J Biol Chem . 2016 Oct 7;291(41):21363-21374
0021-9258
http://hdl.handle.net/20.500.12105/9667
27551041
10.1074/jbc.M116.722587
1083-351X
The Journal of biological chemistry
ER quality control
TRK1-transforming tyrosine kinase protein (Trk-A)
autophagic flux
autophagy
congenital insensitivity to pain with anhidrosis
neurodegeneration
protein aggregation
Mutations in TrkA Causing Congenital Insensitivity to Pain with Anhidrosis (CIPA) Induce Misfolding, Aggregation, and Mutation-dependent Neurodegeneration by Dysfunction of the Autophagic Flux