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再生与重编程的比较。

Regeneration and reprogramming compared.

机构信息

Center for Regenerative Medicine of Barcelona, 08003 Barcelona, Spain.

出版信息

BMC Biol. 2010 Jan 20;8:5. doi: 10.1186/1741-7007-8-5.

DOI:10.1186/1741-7007-8-5
PMID:20089153
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2826312/
Abstract

BACKGROUND

Dedifferentiation occurs naturally in mature cell types during epimorphic regeneration in fish and some amphibians. Dedifferentiation also occurs in the induction of pluripotent stem cells when a set of transcription factors (Oct4, Sox2, Klf4 and c-Myc) is over expressed in mature cell types.

RESULTS

We hypothesised that there are parallels between dedifferentiation or reprogramming of somatic cells to induced pluripotent stem cells and the natural process of dedifferentiation during epimorphic regeneration. We analysed expression levels of the most commonly used pluripotency associated factors in regenerating and non-regenerating tissue and compared them with levels in a pluripotent reference cell. We found that some of the pluripotency associated factors (oct4/pou5f1, sox2, c-myc, klf4, tert, sall4, zic3, dppa2/4 and fut1, a homologue of ssea1) were expressed before and during regeneration and that at least two of these factors (oct4, sox2) were also required for normal fin regeneration in the zebrafish. However these factors were not upregulated during regeneration as would be expected if blastema cells acquired pluripotency.

CONCLUSIONS

By comparing cells from the regeneration blastema with embryonic pluripotent reference cells we found that induced pluripotent stem and blastema cells do not share pluripotency. However, during blastema formation some of the key reprogramming factors are both expressed and are also required for regeneration to take place. We therefore propose a link between partially reprogrammed induced pluripotent stem cells and the half way state of blastema cells and suggest that a common mechanism might be regulating these two processes.

摘要

背景

在鱼类和一些两栖动物的后生性再生过程中,成熟细胞类型会自然发生去分化。当一组转录因子(Oct4、Sox2、Klf4 和 c-Myc)在成熟细胞类型中过表达时,多能干细胞的诱导也会发生去分化。

结果

我们假设体细胞向诱导多能干细胞的去分化或重编程与后生性再生过程中的自然去分化之间存在相似之处。我们分析了再生和非再生组织中最常用的多能相关因子的表达水平,并将其与多能参考细胞中的水平进行了比较。我们发现一些多能相关因子(oct4/pou5f1、sox2、c-myc、klf4、tert、sall4、zic3、dppa2/4 和 fut1,ssea1 的同源物)在再生前和再生过程中表达,并且其中至少有两个因子(oct4、sox2)也是斑马鱼正常鳍再生所必需的。然而,这些因子并没有像在诱导多能干细胞中那样在再生过程中被上调,这表明芽基细胞获得多能性。

结论

通过比较再生芽基细胞与胚胎多能参考细胞,我们发现诱导多能干细胞和芽基细胞不具有多能性。然而,在芽基形成过程中,一些关键的重编程因子既表达,也需要进行再生。因此,我们提出诱导多能干细胞的部分重编程与芽基细胞的中间状态之间存在联系,并提出可能存在共同的机制来调节这两个过程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5999/2826312/eeccc049b6a2/1741-7007-8-5-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5999/2826312/ece57aa41b79/1741-7007-8-5-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5999/2826312/0afaf2b805d8/1741-7007-8-5-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5999/2826312/1be9be3b06da/1741-7007-8-5-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5999/2826312/eeccc049b6a2/1741-7007-8-5-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5999/2826312/ece57aa41b79/1741-7007-8-5-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5999/2826312/0afaf2b805d8/1741-7007-8-5-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5999/2826312/1be9be3b06da/1741-7007-8-5-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5999/2826312/eeccc049b6a2/1741-7007-8-5-4.jpg

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