Endoplasmic reticulum and Golgi stress in microcephaly

被引:26
|
作者
Passemard, Sandrine [1 ,2 ]
Perez, Franck [3 ]
Gressens, Pierre [1 ,4 ]
El Ghouzzi, Vincent [1 ]
机构
[1] Univ Paris, INSERM, NeuroDiderot, F-75019 Paris, France
[2] Hop Robert Debre, AP HP, Serv Genet Clin, F-75019 Paris, France
[3] PSL Res Univ, Inst Curie, UMR144, CNRS, Paris, France
[4] Kings Coll London, Ctr Developing Brain, Div Imaging Sci & Biomed Engn, St Thomas Hosp,Kings Hlth Partners, London, England
关键词
Golgi apparatus; endoplasmic reticulum; stress; UPR; corticogenesis; primary microcephaly; golgipathies; UNFOLDED PROTEIN RESPONSE; NUCLEOTIDE EXCHANGE FACTORS; SIGNALING PATHWAY; SPINDLE ORIENTATION; ZIKA VIRUS; TRANSCRIPTION FACTOR; CONGENITAL DISORDER; GLUCOSE DEPRIVATION; CELL-PROLIFERATION; QUALITY-CONTROL;
D O I
10.15698/cst2019.12.206
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Microcephaly is a neurodevelopmental condition characterized by a small brain size associated with intellectual deficiency in most cases and is one of the most frequent clinical sign encountered in neurodevelopmental disorders. It can result from a wide range of environmental insults occurring during pregnancy or postnatally, as well as from various genetic causes and represents a highly heterogeneous condition. However, several lines of evidence highlight a compromised mode of division of the cortical precursor cells during neurogenesis, affecting neural commitment or survival as one of the common mechanisms leading to a limited production of neurons and associated with the most severe forms of congenital microcephaly. In this context, the emergence of the endoplasmic reticulum (ER) and the Golgi apparatus as key guardians of cellular homeostasis, especially through the regulation of proteostasis, has raised the hypothesis that pathological ER and/or Golgi stress could contribute significantly to cortical impairments eliciting microcephaly. In this review, we discuss recent findings implicating ER and Golgi stress responses in early brain development and provide an overview of microcephaly-associated genes involved in these pathways.
引用
收藏
页码:369 / 384
页数:16
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