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HGF and MET: From Brain Development to Neurological Disorders

Title: HGF and MET: From Brain Development to Neurological Disorders
Authors: Desole C.; Gallo S.; Vitacolonna A.; Montarolo F.; Bertolotto A.; Vivien D.; Comoglio P.; Crepaldi T.
Contributors: Desole C.; Gallo S.; Vitacolonna A.; Montarolo F.; Bertolotto A.; Vivien D.; Comoglio P.; Crepaldi T.
Publication Year: 2021
Collection: Università degli studi di Torino: AperTo (Archivio Istituzionale ad Accesso Aperto)
Subject Terms: amyotrophic lateral sclerosi; autism; cerebral ischemia; HGF; MET; multiple sclerosi; spinal cord injury; synaptogenesis
Description: Hepatocyte growth factor (HGF) and its tyrosine kinase receptor, encoded by the MET cellular proto-oncogene, are expressed in the nervous system from pre-natal development to adult life, where they are involved in neuronal growth and survival. In this review, we highlight, beyond the neurotrophic action, novel roles of HGF-MET in synaptogenesis during post-natal brain development and the connection between deregulation of MET expression and developmental disorders such as autism spectrum disorder (ASD). On the pharmacology side, HGF-induced MET activation exerts beneficial neuroprotective effects also in adulthood, specifically in neurodegenerative disease, and in preclinical models of cerebral ischemia, spinal cord injuries, and neurological pathologies, such as Alzheimer’s disease (AD), amyotrophic lateral sclerosis (ALS), and multiple sclerosis (MS). HGF is a key factor preventing neuronal death and promoting survival through pro-angiogenic, anti-inflammatory, and immune-modulatory mechanisms. Recent evidence suggests that HGF acts on neural stem cells to enhance neuroregeneration. The possible therapeutic application of HGF and HGF mimetics for the treatment of neurological disorders is discussed.
Document Type: article in journal/newspaper
Language: English
Relation: info:eu-repo/semantics/altIdentifier/pmid/34179015; info:eu-repo/semantics/altIdentifier/wos/WOS:000664500100001; volume:9; firstpage:1; lastpage:21; numberofpages:21; journal:FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY; http://hdl.handle.net/2318/1794809; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85108654501
DOI: 10.3389/fcell.2021.683609
Availability: http://hdl.handle.net/2318/1794809; https://doi.org/10.3389/fcell.2021.683609
Rights: info:eu-repo/semantics/openAccess
Accession Number: edsbas.601E5010
Database: BASE