A Point Mutation in Translation Initiation Factor 2B Leads to a Continuous Hyper Stress State in Oligodendroglial-Derived CellsReport as inadecuate




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Background

Mutations in eukaryotic translation initiation factor 2B eIF2B cause Childhood Ataxia with CNS Hypomyelination CACH, also known as Vanishing White Matter disease VWM. The disease is manifested by loss of brain myelin upon physiological stress. In a previous study, we showed that fibroblasts isolated from CACH-VWM patients are hypersensitive to pharmacologically-induced endoplasmic reticulum ER stress. Since brain cells from affected individuals are not available for research, we wished to assess the effect of eIF2B mutation on oligodendroglial-derived cells.

Methodology-Principal Findings

A rat oligodendroglial-derived cell line was used for a stable knock-down of eIF2B5 followed by stable expression of mutated eIF2B5R195H cDNA. In response to a pharmacological ER-stress agent, eIF2B5R195H expressing cells exhibited heightened ER-stress response demonstrated by hyper induction of ATF4, GADD34, Bip, PDIA1, PDIA3, PDIA4 and PDIA6 proteins. Moreover, even in the absence of a pharmacological stress agent, eIF2B5R195H-expressing cells exhibited high basal levels of ATF4, GADD34 and ER-associated Bip, PDIA1 and PDIA3.

Significance

The data provide evidence that oligodendroglial-derived cells expressing a mutated eIF2B constantly use their stress response mechanism as an adaptation mean in order to survive. The current study is the first to demonstrate the effects of eIF2B5 mutation on ER homeostasis in oligodendroglial-derived cells.



Author: Liraz Kantor, Dalia Pinchasi, Michelle Mintz, Yetrib Hathout, Adeline Vanderver, Orna Elroy-Stein

Source: http://plos.srce.hr/



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