Literature DB >> 24628581

Potential neuroprotective role of transforming growth factor β1 (TGFβ1) in the brain.

Alonso Martínez-Canabal1.   

Abstract

TGFβ1 is a growth factor that is known to be expressed in most neurodegenerative diseases and after vascular accidents in the brain. TGFβ1 downregulates the activity of activated microglia and promotes astrogliosis. It also prevents cell death by a known mechanism dependant on astrocytes and the secretion of the plasminogen activator inhibitor 1 (PAI-1). This mechanism can provide light on what is the mechanism of action of TGFβ1 as a protective factor and it can provide the pharmacological principles in which this pathway could be used with therapeutic purposes. TGFβ1 is upregulated in most neurodegenerative diseases, however, its expression appears dramatically blocked in Huntington's disease, the fastest of those diseases in progress after the onset. This fact suggests that TGFβ1 slows down the neurodegenerative process, preventing tissue damage and neural apoptotic death. However, the exact details of TGFβ1 action are still unknown and the physiological roles on the diseases are still mysterious. Interestingly, all the data regarding the roles of TGFβ1 in health and disease have been also confirmed with the use of transgenic knockouts and TGFβ1 overexpressing mice. What possibly came as a surprise from the study of TGFβ1 overexpressing models is that combining its neuroprotective and antiproliferative effects, this cytokine generates a significant disruption in the hippocampal circuitry with its consequent learning and memory deficit.

Entities:  

Keywords:  TGFβ1; brain disease; neurodegeneration

Mesh:

Substances:

Year:  2014        PMID: 24628581     DOI: 10.3109/00207454.2014.903947

Source DB:  PubMed          Journal:  Int J Neurosci        ISSN: 0020-7454            Impact factor:   2.292


  5 in total

1.  Intermittent administration of PTH induces the expression of osteocalcin and BMP-2 on choroid plexus cells associated with suppression of sclerostin, TGF-β1, and Na+K+ATPase.

Authors:  Allan Fernando Giovanini; Isabella Göhringer; Rosangela Tavella; Manuelly Cristiny Linzmeyer; Thaynara Fernanda Priesnitz; Luana Mordask Bonetto; Rafaela Guimarães Resende; Rafaela Scariot; João Cesar Zielak
Journal:  Endocrine       Date:  2017-12-12       Impact factor: 3.633

2.  TGF-β1 is associated with deficits in cognition and cerebral cortical thickness in first-episode schizophrenia.

Authors:  Shujuan Pan; Yanfang Zhou; Ling Yan; Fangling Xuan; Jinghui Tong; Yanli Li; Junchao Huang; Wei Feng; Song Chen; Yimin Cui; Fude Yang; Shuping Tan; Zhiren Wang; Baopeng Tian; L Elliot Hong; Yun-Long Tan; Li Tian
Journal:  J Psychiatry Neurosci       Date:  2022-03-17       Impact factor: 5.699

3.  Induction of microglia activation after infection with the non-neurotropic A/CA/04/2009 H1N1 influenza virus.

Authors:  Shankar Sadasivan; Mark Zanin; Kevin O'Brien; Stacey Schultz-Cherry; Richard J Smeyne
Journal:  PLoS One       Date:  2015-04-10       Impact factor: 3.240

Review 4.  Preclinical and clinical investigations of mood stabilizers for Huntington's disease: what have we learned?

Authors:  Lisa Scheuing; Chi-Tso Chiu; Hsiao-Mei Liao; Gabriel R Linares; De-Maw Chuang
Journal:  Int J Biol Sci       Date:  2014-09-10       Impact factor: 6.580

5.  TGF-β1 Provides Neuroprotection via Inhibition of Microglial Activation in 3-Acetylpyridine-Induced Cerebellar Ataxia Model Rats.

Authors:  Bei-Bei Cao; Xiao-Xian Zhang; Chen-Yu Du; Zhan Liu; Yi-Hua Qiu; Yu-Ping Peng
Journal:  Front Neurosci       Date:  2020-03-20       Impact factor: 4.677

  5 in total

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