Literature DB >> 31891740

The low levels of nerve growth factor and its upstream regulatory kinases in prion infection is reversed by resveratrol.

Chao Hu1, Cao Chen2, Jia Chen3, Kang Xiao4, Jing Wang4, Qi Shi4, Yue Ma5, Li-Ping Gao5, Yue-Zhang Wu5, Lian Liu6, Ying Xia6, Pu Yan6, Adalaiti Maimaitiming5, Dong-Hua Zhou5, Li-Na Zhang5, Zhi-Bao Chen7, Xiao-Ping Dong8.   

Abstract

Resveratrol shows ability to eliminate prion replication, but the exact mechanism for prion eradication was not clear yet. Our previous studies demonstrate a downregulation of brain-derived nerve growth factor (BDNF) during prion infection, meanwhile recovery of cerebral nerve growth factor (NGF) level by resveratrol treatment has been reported in other neurodegenerative models. To obtain the possible changes of brain NGF and its upstream regulatory cascade during prion infection and after removal of prion propagation, the levels of NGF and its upstream regulatory factors in various prion-infected and prion-eradicated SMB cell lines and mice brains inoculated with various SMB cellular lysates were assessed with various methodologies. The levels of NGF were significantly decreased during prion replication, while recovered after removal of PrPSc by resveratrol in vitro. Morphological assays revealed that the NGF signals mainly colocalized within neurons, but not in the proliferative astrocytes and microglia. The upstream positive regulatory kinases, such as p-CREB, p-CaMKIV, CaMKK2 were decreased in the prion infected cells and mice brains, whereas the negative regulatory one, p-CaMKK2, was increased. The aberrant situations of those kinases in prion infected cell lines or mice brains could be also partially reversed by removal of prion agent. Moreover, we demonstrated that the signals of CaMKK2 and p-CaMKK2 were also distributed predominately in neurons in the brain tissues. The data illustrate a direct linkage of abnormally repressive NGF and its upstream regulatory kinases with prion infection. Resveratrol has not only the ability to inhibit prion replication, but also to improve the expression of NGF via CaMKK2/CaMKIV cascade, which might benefit the microenvironment in brains.
Copyright © 2019 Elsevier B.V. and Japan Neuroscience Society. All rights reserved.

Entities:  

Keywords:  CaMKIV; CaMKK2; NGF; Prion; Resveratrol

Mesh:

Substances:

Year:  2019        PMID: 31891740     DOI: 10.1016/j.neures.2019.12.019

Source DB:  PubMed          Journal:  Neurosci Res        ISSN: 0168-0102            Impact factor:   3.304


  2 in total

1.  Enhanced M-CSF/CSF1R Signaling Closely Associates with PrPSc Accumulation in the Scrapie-Infected Cell Line and the Brains of Scrapie-Infected Experimental Rodents.

Authors:  Ying Xia; Cao Chen; Jia Chen; Chao Hu; Wei Yang; Lin Wang; Lian Liu; Li-Ping Gao; Yue-Zhang Wu; Dong-Dong Chen; Qi Shi; Zhi-Bao Chen; Xiao-Ping Dong
Journal:  Mol Neurobiol       Date:  2022-08-15       Impact factor: 5.682

2.  Different Aberrant Changes of mGluR5 and Its Downstream Signaling Pathways in the Scrapie-Infected Cell Line and the Brains of Scrapie-Infected Experimental Rodents.

Authors:  Chao Hu; Cao Chen; Ying Xia; Jia Chen; Wei Yang; Lin Wang; Dong-Dong Chen; Yue-Zhang Wu; Qin Fan; Xiao-Xi Jia; Kang Xiao; Qi Shi; Zhi-Bao Chen; Xiao-Ping Dong
Journal:  Front Cell Dev Biol       Date:  2022-05-12
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.