• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

侧群现象可富集小鼠的特定肾上腺皮质祖细胞。

The side population phenomenon enriches for designated adrenocortical progenitor cells in mice.

机构信息

Endocrine Research Unit, Medizinische Klinik und Poliklinik IV, Klinikum der Universität München, Ziemssenstraße 1, D-80336 Munich, Germany.

出版信息

J Endocrinol. 2012 Dec;215(3):383-91. doi: 10.1530/JOE-12-0393. Epub 2012 Oct 5.

DOI:10.1530/JOE-12-0393
PMID:23042945
Abstract

Somatic adrenal stem cells are believed to reside in the periphery of the adrenal cortex throughout life for organ maintenance. Herein, we used the side population (SP) phenomenon to enrich for these progenitors, which made up to 0.01-0.64% of the total cell count. Microarray analysis revealed an expression profile of SP cells, which clearly differed from that of non-SP cells. However, a promising adrenal specific stem cell marker could not be identified. In vitro, SP cells could be maintained in long-term culture, whereas non-SP cells did not proliferate. After 4 weeks of culturing, immunohistochemistry revealed the expression of steroidogenic enzymes such as 3β-HSD, StAR, and P450SCC, suggesting spontaneous differentiation. Interestingly, the quantity of SP cells was significantly diminished in Pbx1 haploinsufficient mice, suggesting a stem cell deficit. By contrast, the subcapsular zone of ACTH-deficient Tpit(-/-) mice was significantly wider compared with wild-type adrenals (Tpit(-/-) 259±10.7 vs Tpit(+/-) 100±12.3%; P<0.01). Accordingly, the number of SP cells in these mice was significantly higher (Tpit(-/-) 0.45±0.16 vs Tpit(+/-) 0.13±0.04%; P<0.004). ACTH treatment of these animals reverted the subcapsular zone width and the SP fraction back to normal (130±10.2%; P=0.33 and 0.09%), providing indirect evidence for a stem cell 'arrest' in Tpit(-/-) mice and the role of ACTH in adrenocortical stem cell modulation and differentiation.

摘要

体肾上腺干细胞被认为在生命过程中存在于肾上腺皮质的外围,用于器官维持。在此,我们使用侧群(SP)现象来富集这些祖细胞,其占总细胞计数的 0.01-0.64%。微阵列分析显示了 SP 细胞的表达谱,与非 SP 细胞明显不同。然而,未能鉴定出有前途的肾上腺特异性干细胞标志物。在体外,SP 细胞可以在长期培养中维持,而非 SP 细胞则不能增殖。培养 4 周后,免疫组织化学显示出类固醇生成酶如 3β-HSD、StAR 和 P450SCC 的表达,表明自发分化。有趣的是,在 Pbx1 半不足小鼠中 SP 细胞的数量明显减少,表明存在干细胞缺陷。相比之下,ACTH 缺乏性 Tpit(-/-)小鼠的肾上腺被膜下区明显比野生型肾上腺宽(Tpit(-/-) 259±10.7 对 Tpit(+/-) 100±12.3%;P<0.01)。相应地,这些小鼠中的 SP 细胞数量明显更高(Tpit(-/-) 0.45±0.16 对 Tpit(+/-) 0.13±0.04%;P<0.004)。ACTH 处理这些动物使被膜下区宽度和 SP 分数恢复正常(130±10.2%;P=0.33 和 0.09%),为 Tpit(-/-)小鼠中的干细胞“停滞”和 ACTH 在肾上腺皮质干细胞调节和分化中的作用提供了间接证据。

相似文献

1
The side population phenomenon enriches for designated adrenocortical progenitor cells in mice.侧群现象可富集小鼠的特定肾上腺皮质祖细胞。
J Endocrinol. 2012 Dec;215(3):383-91. doi: 10.1530/JOE-12-0393. Epub 2012 Oct 5.
2
[Tpit mutations reveal a new model of pituitary differentiation and account for isolated ACTH deficiency].[促甲状腺激素释放激素诱导蛋白(TPIT)突变揭示了垂体分化的新模式并解释了孤立性促肾上腺皮质激素缺乏症]
Med Sci (Paris). 2004 Nov;20(11):1009-13. doi: 10.1051/medsci/200420111009.
3
Low estriol levels in the maternal triple-marker screen as a predictor of isolated adrenocorticotropic hormone deficiency caused by a new mutation in the TPIT gene.孕妇三联筛查中雌三醇水平低可作为由TPIT基因新突变导致的孤立性促肾上腺皮质激素缺乏症的预测指标。
Pediatrics. 2006 Feb;117(2):e322-7. doi: 10.1542/peds.2005-1973. Epub 2006 Jan 3.
4
Lack of an adrenal cortex in Sf1 mutant mice is compatible with the generation and differentiation of chromaffin cells.在Sf1突变小鼠中肾上腺皮质的缺失与嗜铬细胞的产生和分化是相容的。
Development. 2005 Oct;132(20):4611-9. doi: 10.1242/dev.02052. Epub 2005 Sep 21.
5
Pituitary progenitor cells tracked down by side population dissection.通过侧群细胞分选追踪垂体祖细胞。
Stem Cells. 2009 May;27(5):1182-95. doi: 10.1002/stem.51.
6
The TPIT gene mutation M86R associated with isolated adrenocorticotropin deficiency interferes with protein: protein interactions.与孤立性促肾上腺皮质激素缺乏相关的TPIT基因突变M86R会干扰蛋白质与蛋白质的相互作用。
J Clin Endocrinol Metab. 2007 Oct;92(10):3991-9. doi: 10.1210/jc.2007-0284. Epub 2007 Jul 24.
7
Human and mouse TPIT gene mutations cause early onset pituitary ACTH deficiency.人类和小鼠的促甲状腺激素释放激素(TPIT)基因突变会导致早发性垂体促肾上腺皮质激素(ACTH)缺乏。
Genes Dev. 2003 Mar 15;17(6):711-6. doi: 10.1101/gad.1065603.
8
Myogenic specification of side population cells in skeletal muscle.骨骼肌中侧群细胞的成肌分化
J Cell Biol. 2002 Oct 14;159(1):123-34. doi: 10.1083/jcb.200202092.
9
Expression and spatio-temporal distribution of differentiation and proliferation markers during mouse adrenal development.小鼠肾上腺发育过程中分化和增殖标志物的表达及时空分布
Gene Expr Patterns. 2007 Jan;7(1-2):72-81. doi: 10.1016/j.modgep.2006.05.009. Epub 2006 Jun 3.
10
Loss of retinal progenitor cells leads to an increase in the retinal stem cell population in vivo.视网膜祖细胞的缺失会导致体内视网膜干细胞数量增加。
Eur J Neurosci. 2006 Jan;23(1):75-82. doi: 10.1111/j.1460-9568.2005.04537.x.