{"title":"间充质干细胞用于椎间盘修复的前景","authors":"J. Melrose","doi":"10.15406/JSRT.2017.02.00061","DOIUrl":null,"url":null,"abstract":"Disc degeneration (DD) is a major musculoskeletal condition affecting 80% of the general global population [1]. The associated low back pain (LBP) has major socioeconomic impact reviewed in [2]. In the past 25 years a number of promising biological therapies have been investigated for the treatment of degenerative Disc Disease (DDD) and these have identified many potential molecular targets for biologic intervention [3-5]. These include agents which induce cellular proliferation, matrix production, regulate matrix metallo protease (MMP) and tissue inhibitor of metallo protease (TIMP) production, inflammation, vascular ingrowth and cell viability [6]. The cell density in the IVD is low [7] and disc cells are exposed to a hostile environment of low oxygen tension, high lactic acid levels, low nutrition and a high hydrostatic pressure leading to cell death and a diminution in cell numbers over time due to cellular senescence [8,9], apoptosis [10,11] and autophagy [12,13]. The resultant decline in cell number with DD places severe demands on any therapeutic measures to alleviate this condition.","PeriodicalId":91560,"journal":{"name":"Journal of stem cell research & therapeutics","volume":"65 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2017-02-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"The promise of mesenchymal stem cells for intervertebral disc repair\",\"authors\":\"J. Melrose\",\"doi\":\"10.15406/JSRT.2017.02.00061\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Disc degeneration (DD) is a major musculoskeletal condition affecting 80% of the general global population [1]. The associated low back pain (LBP) has major socioeconomic impact reviewed in [2]. In the past 25 years a number of promising biological therapies have been investigated for the treatment of degenerative Disc Disease (DDD) and these have identified many potential molecular targets for biologic intervention [3-5]. These include agents which induce cellular proliferation, matrix production, regulate matrix metallo protease (MMP) and tissue inhibitor of metallo protease (TIMP) production, inflammation, vascular ingrowth and cell viability [6]. The cell density in the IVD is low [7] and disc cells are exposed to a hostile environment of low oxygen tension, high lactic acid levels, low nutrition and a high hydrostatic pressure leading to cell death and a diminution in cell numbers over time due to cellular senescence [8,9], apoptosis [10,11] and autophagy [12,13]. The resultant decline in cell number with DD places severe demands on any therapeutic measures to alleviate this condition.\",\"PeriodicalId\":91560,\"journal\":{\"name\":\"Journal of stem cell research & therapeutics\",\"volume\":\"65 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2017-02-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of stem cell research & therapeutics\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.15406/JSRT.2017.02.00061\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of stem cell research & therapeutics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.15406/JSRT.2017.02.00061","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
The promise of mesenchymal stem cells for intervertebral disc repair
Disc degeneration (DD) is a major musculoskeletal condition affecting 80% of the general global population [1]. The associated low back pain (LBP) has major socioeconomic impact reviewed in [2]. In the past 25 years a number of promising biological therapies have been investigated for the treatment of degenerative Disc Disease (DDD) and these have identified many potential molecular targets for biologic intervention [3-5]. These include agents which induce cellular proliferation, matrix production, regulate matrix metallo protease (MMP) and tissue inhibitor of metallo protease (TIMP) production, inflammation, vascular ingrowth and cell viability [6]. The cell density in the IVD is low [7] and disc cells are exposed to a hostile environment of low oxygen tension, high lactic acid levels, low nutrition and a high hydrostatic pressure leading to cell death and a diminution in cell numbers over time due to cellular senescence [8,9], apoptosis [10,11] and autophagy [12,13]. The resultant decline in cell number with DD places severe demands on any therapeutic measures to alleviate this condition.