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细胞核硬化抑制侵袭性黑色素瘤细胞的迁移。

Nuclear stiffening inhibits migration of invasive melanoma cells.

作者信息

Ribeiro Alexandre J S, Khanna Payal, Sukumar Aishwarya, Dong Cheng, Dahl Kris Noel

机构信息

Department of Biomedical Engineering, Carnegie Melon University, Pittsburgh, PA 15213.

Department of Bioengineering, The Pennsylvania State University, University Park, PA 16802.

出版信息

Cell Mol Bioeng. 2014 Dec 1;7(4):544-551. doi: 10.1007/s12195-014-0358-3.

Abstract

During metastasis, melanoma cells must be sufficiently deformable to squeeze through extracellular barriers with small pore sizes. We visualize and quantify deformability of single cells using micropipette aspiration and examine the migration potential of a population of melanoma cells using a flow migration apparatus. We artificially stiffen the nucleus with recombinant overexpression of Δ50 lamin A, which is found in patients with Hutchison Gilford progeria syndrome and in aged individuals. Melanoma cells, both WM35 and Lu1205, both show reduced nuclear deformability and reduced cell invasion with the expression of Δ50 lamin A. These studies suggest that cellular aging including expression of Δ50 lamin A and nuclear stiffening may reduce the potential for metastatic cancer migration. Thus, the pathway of cancer metastasis may be kept in check by mechanical factors in addition to known chemical pathway regulation.

摘要

在转移过程中,黑色素瘤细胞必须具有足够的可变形性,以便挤过孔径较小的细胞外屏障。我们使用微量移液器抽吸来可视化和量化单细胞的可变形性,并使用流动迁移装置检查一群黑色素瘤细胞的迁移潜力。我们通过重组过表达Δ50核纤层蛋白A来人为地使细胞核变硬,Δ50核纤层蛋白A在患有哈钦森-吉尔福德早衰综合征的患者和老年人中被发现。WM35和Lu1205这两种黑色素瘤细胞在表达Δ50核纤层蛋白A时均表现出核可变形性降低和细胞侵袭减少。这些研究表明,包括Δ50核纤层蛋白A的表达和核硬化在内的细胞衰老可能会降低转移性癌症迁移的潜力。因此,除了已知的化学途径调节外,癌症转移途径可能还受到机械因素的控制。

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