A potential role for genome structure in the translation of mechanical force during immune cell development

被引:2
|
作者
Jacobson, Elsie [1 ]
Perry, Jo K. [1 ]
Long, David S. [2 ]
Vickers, Mark H. [1 ]
O'Sullivan, Justin M. [1 ]
机构
[1] Univ Auckland, Liggins Inst, Private Bag 92019, Auckland 1142, New Zealand
[2] Univ Auckland, Auckland Bioengn Inst, Auckland, New Zealand
关键词
chromatin; genome biology; Hi-C; immune; mechanosensory; mechanotransduction; nucleus; nuclear lamin; nucleoskeleton; tensegrity; FLUID SHEAR-STRESS; RETINOBLASTOMA GENE-PRODUCT; POSITIVE-FEEDBACK LOOP; TRANSCRIPTION FACTORIES; ENDOTHELIAL-CELL; INTERCHROMOSOMAL ASSOCIATIONS; EXTRACELLULAR-MATRIX; LAMIN-A; NUCLEAR; DIFFERENTIATION;
D O I
10.1080/19491034.2016.1238998
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Immune cells react to a wide range of environments, both chemical and physical. While the former has been extensively studied, there is growing evidence that physical and in particular mechanical forces also affect immune cell behavior and development. In order to elicit a response that affects immune cell behavior or development, environmental signals must often reach the nucleus. Chemical and mechanical signals can initiate signal transduction pathways, but mechanical forces may also have a more direct route to the nucleus, altering nuclear shape via mechanotransduction. The three-dimensional organization of DNA allows for the possibility that altering nuclear shape directly remodels chromatin, redistributing critical regulatory elements and proteins, and resulting in wide-scale gene expression changes. As such, integrating mechanotransduction and genome architecture into the immunology toolkit will improve our understanding of immune development and disease.
引用
收藏
页码:462 / 475
页数:14
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