Department of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark.
PLoS One. 2012;7(4):e33632. doi: 10.1371/journal.pone.0033632. Epub 2012 Apr 16.
Micro-anatomical structures in tissues have potential physiological effects. In arteries and arterioles smooth muscle cells and endothelial cells are separated by the internal elastic lamina, but the two cell layers often make contact through micro protrusions called myoendothelial junctions. Cross talk between the two cell layers is important in regulating blood pressure and flow. We have used a spatiotemporal mathematical model to investigate how the myoendothelial junctions affect the information flow between the two cell layers. The geometry of the model mimics the structure of the two cell types and the myoendothelial junction. The model is implemented as a 2D axi-symmetrical model and solved using the finite element method. We have simulated diffusion of Ca(2+) and IP(3) between the two cell types and we show that the micro-anatomical structure of the myoendothelial junction in itself may rectify a signal between the two cell layers. The rectification is caused by the asymmetrical structure of the myoendothelial junction. Because the head of the myoendothelial junction is separated from the cell it is attached to by a narrow neck region, a signal generated in the neighboring cell can easily drive a concentration change in the head of the myoendothelial protrusion. Subsequently the signal can be amplified in the head, and activate the entire cell. In contrast, a signal in the cell from which the myoendothelial junction originates will be attenuated and delayed in the neck region as it travels into the head of the myoendothelial junction and the neighboring cell.
组织中的微观解剖结构具有潜在的生理效应。在动脉和小动脉中,平滑肌细胞和内皮细胞被内弹性膜隔开,但这两层细胞经常通过称为肌内皮连接的微小突起相互接触。两层细胞之间的串扰对于调节血压和血流非常重要。我们使用时空数学模型研究了肌内皮连接如何影响两层细胞之间的信息流。模型的几何形状模拟了两种细胞类型和肌内皮连接的结构。该模型被实现为二维轴对称模型,并使用有限元方法求解。我们模拟了两种细胞类型之间 Ca(2+)和 IP(3)的扩散,结果表明肌内皮连接的微观解剖结构本身就可以纠正两层细胞之间的信号。这种整流是由肌内皮连接的不对称结构引起的。由于肌内皮连接的头部通过狭窄的颈部区域与附着的细胞分离,因此相邻细胞中产生的信号可以很容易地驱动肌内皮突起头部的浓度变化。随后,信号可以在头部放大,并激活整个细胞。相比之下,来自肌内皮连接起源的细胞中的信号在进入肌内皮连接头部和相邻细胞的颈部区域时会被衰减和延迟。