Flow of a circulating tumor cell and red blood cells in microvessels.

Phys Rev E Stat Nonlin Soft Matter Phys

School of Engineering, Tohoku University, 6-6-01 Aoba, Aoba, Sendai 980-8579, Japan.

Published: December 2015

AI Article Synopsis

  • Understanding circulating tumor cells (CTCs) is crucial for studying metastasis, particularly their interaction with red blood cells (RBCs) in microvessels of different sizes.
  • The research highlights key differences between CTCs and leukocytes, emphasizing how the larger size of CTCs impacts their flow behavior compared to smaller leukocytes, especially in terms of flow mode and velocity.
  • Findings reveal that CTCs can move faster than RBCs under certain conditions, which could enhance our understanding of cancer spread and aid in the development of advanced microfluidic devices.

Article Abstract

Quantifying the behavior of circulating tumor cells (CTCs) in the blood stream is of fundamental importance for understanding metastasis. Here, we investigate the flow mode and velocity of CTCs interacting with red blood cells (RBCs) in various sized microvessels. The flow of leukocytes in microvessels has been described previously; a leukocyte forms a train with RBCs in small microvessels and exhibits margination in large microvessels. Important differences in the physical properties of leukocytes and CTCs result from size. The dimensions of leukocytes are similar to those of RBCs, but CTCs are significantly larger. We investigate numerically the size effects on the flow mode and the cell velocity, and we identify similarities and differences between leukocytes and CTCs. We find that a transition from train formation to margination occurs when (R-a)/t(R)≈1, where R is the vessel radius, a is the cell radius, and t(R) is the thickness of RBCs, but that the motion of RBCs differs from the case of leukocytes. Our results also show that the velocities of CTCs and leukocytes are larger than the average blood velocity, but only CTCs move faster than RBCs for microvessels of R/a≈1.5-2.0. These findings are expected to be useful not only for understanding metastasis, but also for developing microfluidic devices.

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Source
http://dx.doi.org/10.1103/PhysRevE.92.063011DOI Listing

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