高龄供体损害骨髓细胞治疗心脏病的疗效。

Xiaoyin Wang, Junya Takagawa, Daniel J Haddad, Kranthi Pinnamaneni, Yan Zhang, Richard E Sievers, William Grossman, Yerem Yeghiazarians, Matthew L Springer
{"title":"高龄供体损害骨髓细胞治疗心脏病的疗效。","authors":"Xiaoyin Wang,&nbsp;Junya Takagawa,&nbsp;Daniel J Haddad,&nbsp;Kranthi Pinnamaneni,&nbsp;Yan Zhang,&nbsp;Richard E Sievers,&nbsp;William Grossman,&nbsp;Yerem Yeghiazarians,&nbsp;Matthew L Springer","doi":"10.4172/2157-7552.s3-002","DOIUrl":null,"url":null,"abstract":"<p><p>Therapeutic results of clinical autologous bone marrow cell (BMC) therapy trials for cardiac disease have been modest compared to results of BMC implantation into rodent hearts post-myocardial infarction (MI). In clinical trials, autologous BMCs are typically harvested from older patients who have recently suffered an MI. In contrast, experimental studies in rodent models typically utilize donor BMCs isolated from young, healthy, inbred mice that are not the recipients. Using unfractionated BMCs from donor mice at ages of young, middle-aged, and old, we discovered that recipient left ventricular function post-MI was significantly improved by young donor BMC implantation but was only preserved by middle-aged donor BMCs. Notably, old donor BMCs did not slow the decline in recipient post-MI cardiac function, suggesting BMC impairment by advanced donor age. Furthermore, we also show here that BMCs that are therapeutically impaired by donor age can be further impaired by concurrent donor MI. In conclusion, our findings suggest that therapeutic impairment of BMCs by advanced age is one of the important factors that can limit the success of clinical autologous BMC-based therapy.</p>","PeriodicalId":89595,"journal":{"name":"Journal of tissue science & engineering","volume":"S3 ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2011-11-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3366554/pdf/nihms375524.pdf","citationCount":"1","resultStr":"{\"title\":\"Advanced Donor Age Impairs Bone Marrow Cell Therapeutic Efficacy for Cardiac Disease.\",\"authors\":\"Xiaoyin Wang,&nbsp;Junya Takagawa,&nbsp;Daniel J Haddad,&nbsp;Kranthi Pinnamaneni,&nbsp;Yan Zhang,&nbsp;Richard E Sievers,&nbsp;William Grossman,&nbsp;Yerem Yeghiazarians,&nbsp;Matthew L Springer\",\"doi\":\"10.4172/2157-7552.s3-002\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Therapeutic results of clinical autologous bone marrow cell (BMC) therapy trials for cardiac disease have been modest compared to results of BMC implantation into rodent hearts post-myocardial infarction (MI). In clinical trials, autologous BMCs are typically harvested from older patients who have recently suffered an MI. In contrast, experimental studies in rodent models typically utilize donor BMCs isolated from young, healthy, inbred mice that are not the recipients. Using unfractionated BMCs from donor mice at ages of young, middle-aged, and old, we discovered that recipient left ventricular function post-MI was significantly improved by young donor BMC implantation but was only preserved by middle-aged donor BMCs. Notably, old donor BMCs did not slow the decline in recipient post-MI cardiac function, suggesting BMC impairment by advanced donor age. Furthermore, we also show here that BMCs that are therapeutically impaired by donor age can be further impaired by concurrent donor MI. In conclusion, our findings suggest that therapeutic impairment of BMCs by advanced age is one of the important factors that can limit the success of clinical autologous BMC-based therapy.</p>\",\"PeriodicalId\":89595,\"journal\":{\"name\":\"Journal of tissue science & engineering\",\"volume\":\"S3 \",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2011-11-18\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3366554/pdf/nihms375524.pdf\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of tissue science & engineering\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4172/2157-7552.s3-002\",\"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 tissue science & engineering","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4172/2157-7552.s3-002","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

摘要

临床自体骨髓细胞(BMC)治疗心脏病的试验结果与心肌梗死(MI)后骨髓细胞植入啮齿动物心脏的结果相比并不理想。在临床试验中,自体骨髓干细胞通常来自最近遭受心肌梗死的老年患者。相比之下,啮齿动物模型的实验研究通常使用从年轻、健康、近亲繁殖的非受体小鼠中分离的供体骨髓干细胞。使用来自年轻、中年和老年供体小鼠的未分离BMC,我们发现年轻供体BMC植入显著改善心肌梗死后受体左心室功能,但仅保留中年供体BMC。值得注意的是,年老的供体BMC并没有减缓心肌梗死后受者心功能的下降,这表明BMC受损与供体年龄的增加有关。此外,我们还发现,由于供者年龄而导致治疗性损伤的骨髓基质可能会因同时供者心肌梗死而进一步受损。总之,我们的研究结果表明,老年骨髓基质治疗性损伤是限制临床自体骨髓基质治疗成功的重要因素之一。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Advanced Donor Age Impairs Bone Marrow Cell Therapeutic Efficacy for Cardiac Disease.

Therapeutic results of clinical autologous bone marrow cell (BMC) therapy trials for cardiac disease have been modest compared to results of BMC implantation into rodent hearts post-myocardial infarction (MI). In clinical trials, autologous BMCs are typically harvested from older patients who have recently suffered an MI. In contrast, experimental studies in rodent models typically utilize donor BMCs isolated from young, healthy, inbred mice that are not the recipients. Using unfractionated BMCs from donor mice at ages of young, middle-aged, and old, we discovered that recipient left ventricular function post-MI was significantly improved by young donor BMC implantation but was only preserved by middle-aged donor BMCs. Notably, old donor BMCs did not slow the decline in recipient post-MI cardiac function, suggesting BMC impairment by advanced donor age. Furthermore, we also show here that BMCs that are therapeutically impaired by donor age can be further impaired by concurrent donor MI. In conclusion, our findings suggest that therapeutic impairment of BMCs by advanced age is one of the important factors that can limit the success of clinical autologous BMC-based therapy.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信