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关于肾脏近端小管祖细胞存在情况的物种多样性。

Species diversity regarding the presence of proximal tubular progenitor cells of the kidney.

作者信息

Hansson J, Ericsson A E, Axelson H, Johansson M E

机构信息

Lund University.

出版信息

Eur J Histochem. 2016 Feb 5;60(1):2567. doi: 10.4081/ejh.2016.2567.

DOI:10.4081/ejh.2016.2567
PMID:26972712
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4800248/
Abstract

The cellular source for tubular regeneration following kidney injury is a matter of dispute, with reports suggesting a stem or progenitor cells as the regeneration source while linage tracing studies in mice seemingly favor the classical theory, where regeneration is performed by randomly surviving cells. We, and others have previously described a scattered cell population localized to the tubules of human kidney, which increases in number following injury. Here we have characterized the species distribution of these proximal tubular progenitor cells (PTPCs) in kidney tissue from chimpanzee, pig, rat and mouse using a set of human PTPC markers. We detected PTPCs in chimpanzee and pig kidneys, but not in mouse tissue. Also, subjecting mice to the unilateral urethral obstruction model, caused clear signs of tubular injury, but failed to induce the PTPC phenotype in renal tubules.

摘要

肾损伤后肾小管再生的细胞来源存在争议,有报道表明干细胞或祖细胞是再生来源,而小鼠的谱系追踪研究似乎支持经典理论,即再生由随机存活的细胞完成。我们和其他人之前描述过一种散在的细胞群,定位于人肾的肾小管,损伤后数量增加。在这里,我们使用一组人近端肾小管祖细胞(PTPC)标志物,对黑猩猩、猪、大鼠和小鼠肾组织中这些近端肾小管祖细胞的物种分布进行了表征。我们在黑猩猩和猪的肾脏中检测到了PTPC,但在小鼠组织中未检测到。此外,对小鼠进行单侧尿道梗阻模型,虽造成了明显的肾小管损伤迹象,但未能诱导肾小管中的PTPC表型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20a8/4800248/57789fd012b6/ejh-2016-1-2567-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20a8/4800248/0a9f9ef9b335/ejh-2016-1-2567-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20a8/4800248/3fd1a60fb7cf/ejh-2016-1-2567-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20a8/4800248/57789fd012b6/ejh-2016-1-2567-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20a8/4800248/0a9f9ef9b335/ejh-2016-1-2567-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20a8/4800248/3fd1a60fb7cf/ejh-2016-1-2567-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20a8/4800248/57789fd012b6/ejh-2016-1-2567-g003.jpg

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本文引用的文献

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Cell Tissue Res. 2016 Mar;363(3):791-803. doi: 10.1007/s00441-015-2273-x. Epub 2015 Sep 4.
2
How much can the tubule regenerate and who does it? An open question.肾小管能再生多少,又是由谁来完成再生?这是个悬而未决的问题。
Nephrol Dial Transplant. 2016 Aug;31(8):1243-50. doi: 10.1093/ndt/gfv262. Epub 2015 Jul 13.
3
The use of lineage tracing to study kidney injury and regeneration.利用谱系追踪研究肾脏损伤和再生。
Eur J Histochem. 2016 Dec 16;60(4):2758. doi: 10.4081/ejh.2016.2758.
Nat Rev Nephrol. 2015 Jul;11(7):420-31. doi: 10.1038/nrneph.2015.67. Epub 2015 May 12.
4
Origin of regenerating tubular cells after acute kidney injury.急性肾损伤后再生管状细胞的起源。
Proc Natl Acad Sci U S A. 2014 Jan 28;111(4):1533-8. doi: 10.1073/pnas.1316177111. Epub 2014 Jan 13.
5
Evidence for a morphologically distinct and functionally robust cell type in the proximal tubules of human kidney.人肾脏近端小管中形态独特且功能强大的细胞类型的证据。
Hum Pathol. 2014 Feb;45(2):382-93. doi: 10.1016/j.humpath.2013.10.003. Epub 2013 Oct 18.
6
Controversies on the origin of proliferating epithelial cells after kidney injury.肾损伤后增殖上皮细胞起源的争议。
Pediatr Nephrol. 2014 Apr;29(4):673-9. doi: 10.1007/s00467-013-2669-3. Epub 2013 Dec 10.
7
Differentiated kidney epithelial cells repair injured proximal tubule.分化的肾上皮细胞修复受损的近端肾小管。
Proc Natl Acad Sci U S A. 2014 Jan 28;111(4):1527-32. doi: 10.1073/pnas.1310653110. Epub 2013 Oct 14.
8
Human renal stem/progenitor cells repair tubular epithelial cell injury through TLR2-driven inhibin-A and microvesicle-shuttled decorin.人肾干/祖细胞通过 TLR2 驱动的抑制素-A 和微囊泡转运的饰胶蛋白修复肾小管上皮细胞损伤。
Kidney Int. 2013 Mar;83(3):392-403. doi: 10.1038/ki.2012.413. Epub 2013 Jan 16.
9
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J Pathol. 2013 Apr;229(5):645-59. doi: 10.1002/path.4125.
10
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