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Gene expression changes in dorsal root ganglia following peripheral nerve injury: roles in inflammation,cell death and nociception

Gene expression changes in dorsal root ganglia following peripheral nerve injury: roles in inflammation,cell death and nociception

作     者:Sarah L.Martin Adam J.Reid Alexei Verkhratsky Valerio Magnaghi Alessandro Faroni 

作者机构:Blond McIndoe LaboratoriesSchool of Biological SciencesUniversity of Manchester University Hospital of South ManchesterDepartment of Plastic and BurnsManchester Faculty of BiologyMedicine and HealthUniversity of Manchester Department of Pharmacological and Biomolecular SciencesUniversità degli Studi di Milano 

出 版 物:《Neural Regeneration Research》 (中国神经再生研究(英文版))

年 卷 期:2019年第14卷第6期

页      面:939-947页

核心收录:

学科分类:0710[理学-生物学] 1002[医学-临床医学] 1001[医学-基础医学(可授医学、理学学位)] 10[医学] 

基  金:supported by the Hargreaves and Ball Trust,the National Institute for Health Research(II-LA-0313-20003)(to AJR) the Rosetrees Trust,the Academy of Medical Sciences,and the Manchester Regenerative Medicine Network(MaRMN)(to AF and AJR) Progetto Eccellenza from the Italian Ministry of Research(to VM) 

主  题:Gene expression polymerase chain reaction dorsal root ganglia inflammation nociception cell death peripheral nerve injury Schwann cells satellite glial cells nerve regeneration 

摘      要:Subsequent to a peripheral nerve injury, there are changes in gene expression within the dorsal root ganglia in response to the damage. This review selects factors which are well-known to be vital for inflammation, cell death and nociception, and highlights how alterations in their gene expression within the dorsal root ganglia can affect functional recovery. The majority of studies used polymerase chain reaction within animal models to analyse the dynamic changes following peripheral nerve injuries. This review aims to highlight the factors at the gene expression level that impede functional recovery and are hence are potential targets for therapeutic approaches. Where possible the experimental model, specific time-points and cellular location of expression levels are reported.

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