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Amyotrophic lateral sclerosis as a protein level,non-genomic disease:Therapy with S2RM exosome released molecules

Amyotrophic lateral sclerosis as a protein level, non-genomic disease: Therapy with S2RM exosome released molecules

作     者:Greg Maguire 

作者机构:Bio Regenerative SciencesInc.La JollaCA 92037United States 

出 版 物:《World Journal of Stem Cells》 (世界干细胞杂志(英文版)(电子版))

年 卷 期:2017年第9卷第11期

页      面:187-202页

核心收录:

学科分类:1002[医学-临床医学] 100204[医学-神经病学] 10[医学] 

主  题:Amyotrophic lateral sclerosis Proteins Stem cells Extracellular matrix Exposome Heat shock protein Stem cell molecules 

摘      要:Amyotrophic lateral sclerosis(ALS) is a rapidly progressing neurodegenerative disease that leads to death. No effective treatments are currently available. Based on data from epidemiological, etiological, laboratory, and clinical studies, I offer a new way of thinking about ALS and its treatment. This paper describes a host of extrinsic factors, including the exposome, that disrupt the extracellular matrix and protein function such that a spreading, prionlike disease leads to neurodegeneration in the motor tracts. A treatment regimen is described using the stem cell released molecules from a number of types of adult stem cells to provide tissue dependent molecules that restore homeostasis, including proteostasis, in the ALS patient. Because stem cells themselves as a therapeutic are cumbersome and expensive, and when implanted in a host cause aging of the host tissue and often fail to engraft or remain viable, only the S2 RM molecules are used. Rebuilding of the extracellular matrix and repair of the dysfunctional proteins in the ALS patient ensues.

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