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Initiation and developmental dynamics of Wfs1 expression in the context of neural differentiation and ER stress in mouse forebrain
Author(s) -
Tekko Triin,
Lilleväli Kersti,
Luuk Hendrik,
Sütt Silva,
Truu Laura,
Örd Tiit,
Möls Märt,
Vasar Eero
Publication year - 2014
Publication title -
international journal of developmental neuroscience
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.761
H-Index - 88
eISSN - 1873-474X
pISSN - 0736-5748
DOI - 10.1016/j.ijdevneu.2014.03.009
Subject(s) - wolfram syndrome , striatum , biology , synaptophysin , forebrain , in situ hybridization , unfolded protein response , neuroscience , microbiology and biotechnology , endoplasmic reticulum , endocrinology , diabetes insipidus , medicine , gene expression , central nervous system , genetics , dopamine , gene , immunology , immunohistochemistry
Wolframin (Wfs1) is a membrane glycoprotein that resides in the endoplasmic reticulum (ER) and regulates cellular Ca 2+ homeostasis. In pancreas Wfs1 attenuates unfolded protein response (UPR) and protects cells from apoptosis. Loss of Wfs1 function results in Wolfram syndrome (OMIM 222300) characterized by early‐onset diabetes mellitus, progressive optic atrophy, diabetes insipidus, deafness, and psychiatric disorders. Similarly, Wfs1 −/− mice exhibit diabetes and increased basal anxiety. In the adult central nervous system Wfs1 is prominent in central extended amygdala, striatum and hippocampus, brain structures largely involved in behavioral adaptation of the organism. Here, we describe the initiation pattern of Wfs1 expression in mouse forebrain using mRNA in situ hybridization and compare it with Synaptophysin ( Syp1 ), a gene encoding synaptic vesicle protein widely used as neuronal differentiation marker. We show that the expression of Wfs1 starts during late embryonic development in the dorsal striatum and amygdala, then expands broadly at birth, possessing several transitory regions during maturation. Syp1 expression precedes Wfs1 and it is remarkably upregulated during the period of Wfs1 expression initiation and maturation, suggesting relationship between neural activation and Wfs1 expression. Using in situ hybridization and quantitative real‐time PCR we show that UPR‐related genes ( Grp78 , Grp94 , and Chop ) display dynamic expression in the perinatal brain when Wfs1 is initiated and their expression pattern is not altered in the brain lacking functional Wfs1.