Expression and distribution of JNK/SAPK-associated scaffold protein JS']JSAP1 in developing and adult mouse brain

被引:83
|
作者
Miura, Eriko
Fukaya, Masahiro
Sato, Tokiharu
Sugihara, Kazushi
Asano, Masahide
Yoshioka, Katsuji
Watanabe, Masahiko [1 ]
机构
[1] Hokkaido Univ, Sch Med, Dept Anat, Sapporo, Hokkaido 0608638, Japan
[2] Kanazawa Univ, Inst Canc Res, Dept Mol & Cellular Biol, Kanazawa, Ishikawa, Japan
[3] Kanazawa Univ, Adv Sci Res Ctr, Kanazawa, Ishikawa, Japan
关键词
brain; immunoblot; immunohistochemistry; in situ hybridization; !text type='JS']JS[!/text]AP1; JIP3;
D O I
10.1111/j.1471-4159.2006.03835.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The c-Jun N-terminal kinase (JNK) is one of the three major mitogen-activated protein kinases (MAPKs) playing key roles in various cellular processes in response to both extracellular and intracellular stimuli. JNK/SAPK-associated protein 1 (JSAP1 also referred to as JIP3) is a JNK-associated scaffold that controls the specificity and efficiency of JNK signaling cascades. Here we studied its expression in mouse brains. JSAP1 mRNA was expressed in developing and adult brains, showing spatial patterns similar to JNK1-3 mRNAs. In embryos, JSAP1 immunolabeling was intense for progenitor cells in the ventricular zone throughout the brain and in the external granular layer of the cerebellum, and for neurons and glial cells differentiating in the mantle zone. In adults, JSAP1 was distributed in various neurons and Bergmann glia, with higher levels in striatal cholinergic interneurons, telencephalic parvalbumin-positive interneurons and cerebellar Purkinje cells. In these neurons, JSAP1 was observed as tiny particulate staining in spines, dendrites, perikarya and axons, where it was often associated with the smooth endoplasmic reticulum (sER) and cell membrane. Immunoblots revealed enriched distribution in the microsomal fraction and cytosolic fraction. Therefore, the characteristic cellular expression and subcellular distribution of JSAP1 might be beneficial for cells to efficiently link external stimuli to the JNK MAPK pathway and other intracellular machineries.
引用
收藏
页码:1431 / 1446
页数:16
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