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Expression of Wnt5a and its receptor Fzd2 is changed in the spinal cord of adult amyotrophic lateral sclerosis transgenic mice
被引:0
|作者:
Li, Xiaojin
[1
]
Guan, Yingjun
[1
]
Chen, Yanchun
[1
]
Zhang, Caixia
[1
]
Shi, Caixing
[1
]
Zhou, Fenghua
[1
]
Yu, Li
[1
]
Juan, Juan
[1
]
Wang, Xin
[2
]
机构:
[1] Weifang Med Univ, Dept Histol & Embryol, Shandong 261053, Peoples R China
[2] Harvard Univ, Sch Med, Brigham & Womens Hosp, Dept Neurosurg, Boston, MA USA
来源:
基金:
中国国家自然科学基金;
关键词:
ALS;
Wnt5a;
Fzd2;
NSC34;
astrocyte;
Wnt signaling pathway;
SIGNALING PATHWAY;
BETA-CATENIN;
BINDING;
TUMORS;
D O I:
暂无
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Wnt5a, a member of the Wnt gene family, encodes a cysteine-rich growth factor involved in signal transduction during growth and differentiation. The Fzd2 gene codes for a cell membrane receptor called Frizzled-2 have a structure similar to G protein coupled receptors. The extracellular N-terminal of the Fzd2 receptor has a cysteine-rich domain (CRD) that binds Wnt ligands and thus primes the Wnt signal pathway. Downregulation of the Wnt signal pathway occurs in neurodegenerative diseases including Amyotrophic Lateral Sclerosis (ALS). However, little is known about Wnt5a/Fzd2 signaling in mammalian nerve cells, and it is not clear whether Wnt5a or Fzd2 functioning are changed in ALS. The influence of Wnt5a and Fzd2 signal transduction pathway on ALS was investigated in adult SOD1(G93A) transgenic mice. Changes in Wnt5a and Fzd2 expression in the spinal cord of SOD1(G93A) transgenic mice (ALS), SOD1(G93A) transfected NSC-34 cells, and primary cultures of astrocytes from SOD1(G93A) transgenic mice were detected by immunofluorescent staining, Reverse Transcription-Polymerase Chain Reaction (RT-PCR) and Western blotting. The results provide further insight into the role of Wnt5a and Fzd2 in the pathogenesis of ALS transgenic mice, which provides evidence that should help in the search for treatments of ALS.
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页码:1245 / 1260
页数:16
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