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衰老对人心脏干细胞数量和质量的影响。

Influence of aging on the quantity and quality of human cardiac stem cells.

作者信息

Nakamura Tamami, Hosoyama Tohru, Kawamura Daichi, Takeuchi Yuriko, Tanaka Yuya, Samura Makoto, Ueno Koji, Nishimoto Arata, Kurazumi Hiroshi, Suzuki Ryo, Ito Hiroshi, Sakata Kensuke, Mikamo Akihito, Li Tao-Sheng, Hamano Kimikazu

机构信息

Department of Surgery and Clinical Science, Yamaguchi University Graduate School of Medicine, 1-1-1 Minami-kogushi, Yamaguchi, Ube 755-8505, Japan.

Center for Regenerative Medicine, Yamaguchi University Graduate School of Medicine, 1-1-1 Minami-kogushi, Yamaguchi, Ube 755-8505, Japan.

出版信息

Sci Rep. 2016 Mar 7;6:22781. doi: 10.1038/srep22781.

DOI:10.1038/srep22781
PMID:26947751
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4780032/
Abstract

Advanced age affects various tissue-specific stem cells and decreases their regenerative ability. We therefore examined whether aging affected the quantity and quality of cardiac stem cells using cells obtained from 26 patients of various ages (from 2 to 83 years old). We collected fresh right atria and cultured cardiosphere-derived cells (CDCs), which are a type of cardiac stem cell. Then we investigated growth rate, senescence, DNA damage, and the growth factor production of CDCs. All samples yielded a sufficient number of CDCs for experiments and the cellular growth rate was not obviously associated with age. The expression of senescence-associated b-galactosidase and the DNA damage marker, gH2AX, showed a slightly higher trend in CDCs from older patients (≥ 65 years). The expression of VEGF, HGF, IGF-1, SDF-1, and TGF-b varied among samples, and the expression of these beneficial factors did not decrease with age. An in vitro angiogenesis assay also showed that the angiogenic potency of CDCs was not impaired, even in those from older patients. Our data suggest that the impact of age on the quantity and quality of CDCs is quite limited. These findings have important clinical implications for autologous stem cell transplantation in elderly patients.

摘要

高龄会影响各种组织特异性干细胞,并降低其再生能力。因此,我们使用从26名不同年龄(2至83岁)患者获取的细胞,研究衰老是否会影响心脏干细胞的数量和质量。我们收集新鲜右心房并培养心脏球衍生细胞(CDC),这是一种心脏干细胞。然后我们研究了CDC的生长速率、衰老、DNA损伤和生长因子产生情况。所有样本都产生了足够数量的用于实验的CDC,并且细胞生长速率与年龄没有明显关联。衰老相关β-半乳糖苷酶和DNA损伤标志物γH2AX的表达在老年患者(≥65岁)的CDC中呈略高趋势。VEGF、HGF、IGF-1、SDF-1和TGF-β的表达在样本间有所不同,并且这些有益因子的表达不会随年龄降低。体外血管生成试验还表明,即使是老年患者的CDC,其血管生成能力也未受损。我们的数据表明,年龄对CDC数量和质量的影响相当有限。这些发现对老年患者自体干细胞移植具有重要的临床意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/996f/4780032/3140fee1909b/srep22781-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/996f/4780032/01834edb1585/srep22781-f1.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/996f/4780032/602884c0da43/srep22781-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/996f/4780032/115184848478/srep22781-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/996f/4780032/d9b96a82f07a/srep22781-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/996f/4780032/3140fee1909b/srep22781-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/996f/4780032/01834edb1585/srep22781-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/996f/4780032/37af067dbea8/srep22781-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/996f/4780032/d2417c9b0720/srep22781-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/996f/4780032/602884c0da43/srep22781-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/996f/4780032/115184848478/srep22781-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/996f/4780032/d9b96a82f07a/srep22781-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/996f/4780032/3140fee1909b/srep22781-f7.jpg

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Relative roles of CD90 and c-kit to the regenerative efficacy of cardiosphere-derived cells in humans and in a mouse model of myocardial infarction.CD90和c-kit对人心肌球衍生细胞及小鼠心肌梗死模型再生功效的相对作用
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