4.6 Review Book Chapter

Mechanical Regulation of Nuclear Structure and Function

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ANNUAL REVIEWS
DOI: 10.1146/annurev-bioeng-071910-124638

关键词

nucleus; mechanotransduction; chromatin organization; LINC complex; osmotic stress

资金

  1. NIAMS NIH HHS [AR50245, P01 AR050245, R01 AR048852, R01 AR048182, AR48852, AR48182] Funding Source: Medline
  2. NIA NIH HHS [R01 AG015768, AG15768] Funding Source: Medline
  3. Engineering and Physical Sciences Research Council [EP/E046975/1] Funding Source: researchfish
  4. NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES [R01AR048852, R01AR048182, P01AR050245] Funding Source: NIH RePORTER
  5. NATIONAL INSTITUTE ON AGING [R01AG015768] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Mechanical loading induces both nuclear distortion and alterations in gene expression in a variety of cell types. Mechanotransduction is the process by which extracellular mechanical forces can activate a number of well-studied cytoplasmic signaling cascades. Inevitably, such signals are transduced to the nucleus and induce transcription factor-mediated changes in gene expression. However, gene expression also can be regulated through alterations in nuclear architecture, providing direct control of genome function. One putative transduction mechanism for this phenomenon involves alterations in nuclear architecture that result from the mechanical perturbation of the cell. This perturbation is associated with direct mechanical strain or osmotic stress, which is transferred to the nucleus. This review describes the current state of knowledge relating the nuclear architecture and the transfer of mechanical forces to the nucleus mediated by the cytoskeleton, the nucleoskeleton, and the LINC (linker of the nucleoskeleton and cytoskeleton) complex. Moreover, remodeling of the nucleus induces alterations in nuclear stiffness, which may be associated with cell differentiation. These phenomena are discussed in relation to the potential influence of nuclear architecture-mediated mechanoregulation of transcription and cell fate.

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