Suppr超能文献

小鼠肾脏直部富含线粒体的细胞群体。

A population of mitochondrion-rich cells in the pars recta of mouse kidney.

作者信息

Forbes M S, Thornhill B A, Galarreta C I, Chevalier R L

机构信息

Division of Pediatric Nephrology, Department of Pediatrics, University of Virginia School of Medicine, Charlottesville, VA, 22908, USA.

出版信息

Cell Tissue Res. 2016 Mar;363(3):791-803. doi: 10.1007/s00441-015-2273-x. Epub 2015 Sep 4.

Abstract

Following perfusion of adult mouse kidney with a solution of nitroblue tetrazolium (NBT), certain epithelial cells in the pars recta (S3) segments of proximal tubules react to form cytoplasmic deposits of blue diformazan particles. Such cells are characterized by dark cytoplasm, small and often elliptical nuclei, elaborate, process-bearing profiles, and abundant mitochondria. The atypical epithelial cells display the additional characteristic of immunoreactivity for a wide spectrum of antigens, including mesenchymal proteins such as vimentin. Though present in kidneys of untreated or sham-operated animals, they are particularly evident under experimental conditions such as unilateral ureteral obstruction (UUO), appearing in both contralateral and obstructed kidneys over the course of a week's duration, but disappearing from the obstructed kidney as it undergoes the profound atrophy attributable to deterioration of the population of its proximal tubules. The cells do not appear in neonatal kidneys, even those undergoing UUO, but begin to be recognizable soon after weaning (28 days). It is possible that diformazan-positive cells in the mouse S3 tubular segment constitute a resident population of cells that can replenish or augment the tubule. Although somewhat similar cells, with dark cytoplasm and vimentin expression, have been described in human, rat, and transgenic mouse kidney (Smeets et al. in J Pathol 229: 645-659, 2013; Berger et al. in Proc Natl Acad Sci U S A 111: 1533-1538, 2014), those cells-known as "scattered tubule cells" or "proximal tubule rare cells"- differ from the S3-specific cells in that they are present throughout the entire proximal tubule, often lack a brush border, and have only a few mitochondria.

摘要

用硝基蓝四氮唑(NBT)溶液灌注成年小鼠肾脏后,近端小管直部(S3)段的某些上皮细胞会发生反应,形成蓝色甲臜颗粒的细胞质沉积物。这些细胞的特征是细胞质深色、细胞核小且常呈椭圆形、轮廓精细且有突起,以及线粒体丰富。非典型上皮细胞还具有对多种抗原免疫反应的额外特征,包括波形蛋白等间充质蛋白。虽然在未处理或假手术动物的肾脏中也存在,但在诸如单侧输尿管梗阻(UUO)等实验条件下它们特别明显,在一周的时间内出现在对侧和梗阻侧肾脏中,但随着梗阻侧肾脏因近端小管细胞群的恶化而发生严重萎缩,这些细胞会从梗阻侧肾脏中消失。这些细胞在新生肾脏中不存在,即使是经历UUO的新生肾脏也没有,但在断奶后不久(28天)就开始变得可识别。小鼠S3肾小管段中的甲臜阳性细胞有可能构成一个能够补充或增加肾小管的常驻细胞群。尽管在人类、大鼠和转基因小鼠肾脏中已经描述了一些细胞质深色且表达波形蛋白的类似细胞(Smeets等人,《病理学杂志》229: 645 - 659, 2013;Berger等人,《美国国家科学院院刊》111: 1533 - 1538, 2014),但那些被称为“散在肾小管细胞”或“近端肾小管稀有细胞”的细胞与S3特异性细胞不同,因为它们存在于整个近端小管中,通常缺乏刷状缘,并且只有少数线粒体。

相似文献

1
A population of mitochondrion-rich cells in the pars recta of mouse kidney.
Cell Tissue Res. 2016 Mar;363(3):791-803. doi: 10.1007/s00441-015-2273-x. Epub 2015 Sep 4.
4
5
Proximal tubular injury and rapid formation of atubular glomeruli in mice with unilateral ureteral obstruction: a new look at an old model.
Am J Physiol Renal Physiol. 2011 Jul;301(1):F110-7. doi: 10.1152/ajprenal.00022.2011. Epub 2011 Mar 23.
6
Renal cilia display length alterations following tubular injury and are present early in epithelial repair.
Nephrol Dial Transplant. 2008 Mar;23(3):834-41. doi: 10.1093/ndt/gfm743. Epub 2007 Oct 25.
8
Regulation of MUTYH, a DNA Repair Enzyme, in Renal Proximal Tubular Epithelial Cells.
Oxid Med Cell Longev. 2015;2015:682861. doi: 10.1155/2015/682861. Epub 2015 Oct 20.
10
TIMP-1 gene expression and PAI-1 antigen after unilateral ureteral obstruction in the adult male rat.
Kidney Int. 2000 Sep;58(3):1186-201. doi: 10.1046/j.1523-1755.2000.00274.x.

引用本文的文献

1
Mitochondria-derived vesicles and their potential roles in kidney stone disease.
J Transl Med. 2023 May 2;21(1):294. doi: 10.1186/s12967-023-04133-3.
3
Species diversity regarding the presence of proximal tubular progenitor cells of the kidney.
Eur J Histochem. 2016 Feb 5;60(1):2567. doi: 10.4081/ejh.2016.2567.
4
Prognostic factors and biomarkers of congenital obstructive nephropathy.
Pediatr Nephrol. 2016 Sep;31(9):1411-20. doi: 10.1007/s00467-015-3291-3. Epub 2015 Dec 14.

本文引用的文献

1
The swan-neck lesion: proximal tubular adaptation to oxidative stress in nephropathic cystinosis.
Am J Physiol Renal Physiol. 2015 May 15;308(10):F1155-66. doi: 10.1152/ajprenal.00591.2014. Epub 2015 Feb 18.
2
Acute kidney injury and chronic kidney disease as interconnected syndromes.
N Engl J Med. 2014 Jul 3;371(1):58-66. doi: 10.1056/NEJMra1214243.
3
Origin of regenerating tubular cells after acute kidney injury.
Proc Natl Acad Sci U S A. 2014 Jan 28;111(4):1533-8. doi: 10.1073/pnas.1316177111. Epub 2014 Jan 13.
4
Evidence for a morphologically distinct and functionally robust cell type in the proximal tubules of human kidney.
Hum Pathol. 2014 Feb;45(2):382-93. doi: 10.1016/j.humpath.2013.10.003. Epub 2013 Oct 18.
5
Megalin in acute kidney injury: foe and friend.
Am J Physiol Renal Physiol. 2014 Jan;306(2):F147-54. doi: 10.1152/ajprenal.00378.2013. Epub 2013 Nov 6.
6
Chronic unilateral ureteral obstruction in the neonatal mouse delays maturation of both kidneys and leads to late formation of atubular glomeruli.
Am J Physiol Renal Physiol. 2013 Dec 15;305(12):F1736-46. doi: 10.1152/ajprenal.00152.2013. Epub 2013 Oct 9.
7
EMT-MET in renal disease: should we curb our enthusiasm?
Cancer Lett. 2013 Nov 28;341(1):24-9. doi: 10.1016/j.canlet.2013.04.018. Epub 2013 Apr 21.
8
Of mice and men: the riddle of tubular regeneration.
J Pathol. 2013 Apr;229(5):641-4. doi: 10.1002/path.4162. Epub 2013 Feb 11.
10
Repair of injured proximal tubule does not involve specialized progenitors.
Proc Natl Acad Sci U S A. 2011 May 31;108(22):9226-31. doi: 10.1073/pnas.1100629108. Epub 2011 May 16.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验