Knockdown of TRPV2 inhibits the migration of RAW264.7 cells toward low fluid shear stress region

Author:

Gao Yan1,Zhang Xiao2,Huo Bo1ORCID

Affiliation:

1. Sports Biomechanics Center, Sports Artificial Intelligence Institute Capital University of Physical Education and Sports Beijing People's Republic of China

2. Biomechanics Lab, Department of Mechanics, School of Aerospace Engineering Beijing Institute of Technology Beijing People's Republic of China

Abstract

AbstractOur previous studies have demonstrated that macrophages (RAW264.7) have a special ability for sensing the gradient of fluid shear stress (FSS) and migrate toward the low‐FSS region. However, the molecular mechanism regulating this phenomenon is still unclear. In this study, we examined the transcriptome genes in RAW264.7 cells, MC3T3‐E1 osteoblasts, mesenchymal stem cells, canine renal epithelial cells, and periodontal ligament cells. The expression levels of genes related to cell migration, force transfer, and force sensitivity in the Ca2+ signaling pathway were analyzed. We observed that the transient receptor potential cation channel type 2 (TRPV2) was highly expressed in RAW264.7 cells. Furthermore, we used lentiviral transfection to knockdown TRPV2 expression in RAW264.7 cells and studied the effect of TRPV2 on the migration of RAW264.7 cells under a gradient FSS field. The results showed that compared with normal cells, TRPV2‐knockdown cells had impaired ability for sensing FSS gradient to migrate toward the low‐FSS region and lower intracellular calcium response to FSS stimulation. This study may reveal the molecular mechanism of regulating the directional migration of macrophages under a gradient FSS field.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Cell Biology,Molecular Biology,Biochemistry

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