Karamichos Dimitris, Lakshman Neema, Petroll W Matthew
Department of Ophthalmology, University of Texas Southwestern Medical Center, Dallas, TX 75390-9057, USA.
Invest Ophthalmol Vis Sci. 2007 Nov;48(11):5030-7. doi: 10.1167/iovs.07-0443.
To investigate how extracellular matrix mechanical properties influence cell and matrix patterning in three-dimensional culture.
Human corneal fibroblasts were seeded within 30 x 10 mm collagen matrices that were unconstrained (UN), fully constrained (CO) along the long axis by attaching the construct to two immobilized plastic bars, or partially constrained (PC) by allowing linear elastic displacement of one bar. After 24 hours, constructs were labeled with phalloidin and were imaged using fluorescent and reflected light (for collagen) confocal microscopy. Cell morphology and local collagen fibril density and alignment were measured using digital image processing.
Corneal fibroblasts in UN matrices were less elongated (UN < PC < CO; P < 0.05) than those in constrained matrices. Cells were aligned parallel to the long axis in the anisotropic region of constrained matrices but were randomly aligned in unconstrained (isotropic) matrices (UN < PC = CO; P < 0.05). Both the local collagen density and the degree of cell/collagen coalignment were higher in constrained matrices (UN < PC < CO; P < 0.05). In regions of higher cell density, additional bands of aligned collagen were often observed between individual cells.
These data suggest that cell spreading, alignment, and contractile force generation are directly influenced by the mechanical properties of the surrounding extracellular matrix (ECM). Corneal fibroblasts generally align and compact collagen parallel to the axis of greatest ECM stiffness. Mechanical cross-talk between adjacent cells leads to enhancement of matrix reorganization, and results in additional, more complex matrix patterning.
研究细胞外基质的力学特性如何影响三维培养中的细胞和基质模式。
将人角膜成纤维细胞接种于30×10mm的胶原基质中,该基质无约束(UN)、通过将构建体附着于两根固定的塑料棒沿长轴完全约束(CO)或通过允许一根棒线性弹性位移进行部分约束(PC)。24小时后,用鬼笔环肽标记构建体,并使用荧光和反射光(用于胶原)共聚焦显微镜成像。使用数字图像处理测量细胞形态、局部胶原纤维密度和排列。
无约束基质中的角膜成纤维细胞比受约束基质中的细胞伸长程度小(UN<PC<CO;P<0.05)。在受约束基质的各向异性区域,细胞沿长轴平行排列,但在无约束(各向同性)基质中随机排列(UN<PC = CO;P<0.05)。受约束基质中的局部胶原密度和细胞/胶原共排列程度均较高(UN<PC<CO;P<0.05)。在细胞密度较高的区域,单个细胞之间常观察到额外的排列胶原带。
这些数据表明,细胞铺展、排列和收缩力的产生直接受周围细胞外基质(ECM)力学特性的影响。角膜成纤维细胞通常沿ECM刚度最大的轴平行排列并压实胶原。相邻细胞之间的机械相互作用导致基质重组增强,并导致额外的、更复杂的基质模式。