| Literature DB >> 33917816 |
Xin Jiang1, Yingjun Guan1, Zhenhan Zhao1, Fandi Meng1, Xuemei Wang1, Xueshuai Gao1, Jinmeng Liu1, Yanchun Chen1, Fenghua Zhou1,2, Shuanhu Zhou3, Xin Wang4.
Abstract
The WNT signaling pathway plays an important role in the physiological and pathophysiological processes of the central nervous system and the neurodegenerative disease amyotrophic lateral sclerosis (ALS). We reviewed the literature pertinent to WNT/β-catenin signaling in ALS from cellular studies, animal models, and human clinical trials. WNT, WNT receptors, and other components of the WNT signaling pathway are expressed in both ALS patients and transgenic mice, and are involved in the pathogenesis of ALS. Studies have shown that abnormal activation of the WNT/β-catenin signaling pathway is related to neuronal degeneration and glial cell proliferation. WNT/Ca2+ signaling is associated with the pro-inflammatory phenotype of microglia; data on the muscle skeletal receptor Tyr kinase receptor in superoxide dismutase-1-G93A mice indicate that gene therapy is necessary for successful treatment of ALS. The varying profiles of lipoprotein receptor-related protein 4 antibodies in different ethnic groups suggest that individual treatment and multifactorial personalized approaches may be necessary for effective ALS therapy. In conclusion, the WNT signaling pathway is important to the ALS disease process, making it a likely therapeutic target.Entities:
Keywords: WNT signaling; amyotrophic lateral sclerosis; glial cells; motor neurons; neuromuscular junctions
Year: 2021 PMID: 33917816 DOI: 10.3390/cells10040839
Source DB: PubMed Journal: Cells ISSN: 2073-4409 Impact factor: 6.600