Suppr超能文献

1型神经纤维瘤病单倍体不足培养成纤维细胞对亚微米形貌的部分失明表明神经纤维瘤蛋白在机械传感调节中的新功能。

Partial Blindness to Submicron Topography in NF1 Haploinsufficient Cultured Fibroblasts Indicates a New Function of Neurofibromin in Regulation of Mechanosensoric.

作者信息

Kaufmann D, Hoesch J, Su Y, Deeg L, Mellert K, Spatz J P, Kemkemer R

机构信息

Institute of Human Genetics, University of Ulm, Ulm, Stuttgart, Germany.

出版信息

Mol Syndromol. 2012 Oct;3(4):169-79. doi: 10.1159/000342698. Epub 2012 Sep 27.

Abstract

Cells sense physical properties of their extracellular environment and translate them into biochemical signals. In this study, cell responses to surfaces with submicron topographies were investigated in cultured human NF1 haploinsufficient fibroblasts. Age-matched fibroblasts from 8 patients with neurofibromatosis type 1 (NF1(+/-)) and 9 controls (NF1(+/+)) were cultured on surfaces with grooves of 200 nm height and lateral distance of 2 μm. As cellular response indicator, the mean cell orientation along microstructured grooves was systematically examined. The tested NF1 haploinsufficient fibroblasts were significantly less affected by the topography than those from healthy donors. Incubation of the NF1(+/-) fibroblasts with the farnesyltransferase inhibitor FTI-277 and other inhibitors of the neurofibromin pathway ameliorates significantly the cell orientation. These data indicate that NF1 haploinsufficiency results in an altered response to specific surface topography in fibroblasts. We suggest a new function of neurofibromin in the sensoric mechanism to topographies and a partial mechanosensoric blindness by NF1 haploinsufficiency.

摘要

细胞感知其细胞外环境的物理特性并将其转化为生化信号。在本研究中,在培养的人类NF1单倍体不足的成纤维细胞中研究了细胞对具有亚微米形貌的表面的反应。将来自8名1型神经纤维瘤病患者(NF1(+/-))和9名对照(NF1(+/+))的年龄匹配的成纤维细胞培养在具有200 nm高度和2 μm横向距离的沟槽的表面上。作为细胞反应指标,系统地检查了沿微结构沟槽的平均细胞取向。与健康供体的成纤维细胞相比,测试的NF1单倍体不足的成纤维细胞受形貌的影响明显较小。用法尼基转移酶抑制剂FTI-277和神经纤维瘤蛋白途径的其他抑制剂孵育NF1(+/-)成纤维细胞可显著改善细胞取向。这些数据表明,NF1单倍体不足导致成纤维细胞对特定表面形貌的反应改变。我们提出了神经纤维瘤蛋白在对形貌的传感机制中的新功能,以及NF1单倍体不足导致的部分机械传感失明。

相似文献

2
Restoring functional neurofibromin by protein transduction.
Sci Rep. 2018 Apr 18;8(1):6171. doi: 10.1038/s41598-018-24310-5.
6
Neurofibromin as a regulator of melanocyte development and differentiation.
J Cell Sci. 2008 Jan 15;121(Pt 2):167-77. doi: 10.1242/jcs.013912. Epub 2007 Dec 18.
8
Neurofibromin haploinsufficiency results in altered spermatogenesis in a mouse model of neurofibromatosis type 1.
PLoS One. 2018 Dec 20;13(12):e0208835. doi: 10.1371/journal.pone.0208835. eCollection 2018.
10
The tumor suppressor neurofibromin confers sensitivity to apoptosis by Ras-dependent and Ras-independent pathways.
Cell Death Differ. 2007 May;14(5):895-906. doi: 10.1038/sj.cdd.4402057. Epub 2006 Nov 10.

引用本文的文献

1
Restoring functional neurofibromin by protein transduction.
Sci Rep. 2018 Apr 18;8(1):6171. doi: 10.1038/s41598-018-24310-5.

本文引用的文献

1
SPRED proteins provide a NF-ty link to Ras suppression.
Genes Dev. 2012 Jul 15;26(14):1515-9. doi: 10.1101/gad.197434.112.
3
Pathogenesis of plexiform neurofibroma: tumor-stromal/hematopoietic interactions in tumor progression.
Annu Rev Pathol. 2012;7:469-95. doi: 10.1146/annurev-pathol-011811-132441. Epub 2011 Nov 7.
4
Neurofibromatosis-1 regulates mTOR-mediated astrocyte growth and glioma formation in a TSC/Rheb-independent manner.
Proc Natl Acad Sci U S A. 2011 Sep 20;108(38):15996-6001. doi: 10.1073/pnas.1019012108. Epub 2011 Sep 6.
5
Clinical manifestations of mutations in RAS and related intracellular signal transduction factors.
Curr Opin Pediatr. 2011 Aug;23(4):443-51. doi: 10.1097/MOP.0b013e32834881dd.
6
Multiple increased osteoclast functions in individuals with neurofibromatosis type 1.
Am J Med Genet A. 2011 May;155A(5):1050-9. doi: 10.1002/ajmg.a.33965. Epub 2011 Apr 4.
7
The pathoetiology of neurofibromatosis 1.
Am J Pathol. 2011 May;178(5):1932-9. doi: 10.1016/j.ajpath.2010.12.056. Epub 2011 Mar 31.
8
Mechanisms of mechanical signaling in development and disease.
J Cell Sci. 2011 Jan 1;124(Pt 1):9-18. doi: 10.1242/jcs.071001.

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