Open Access

ABSTRACT

The Rate of Fluid Shear Stress is a Potent Regulator for Lineage Commitment of Mesenchymal Stem Cells Through Modulating [Ca2+]i, F-actin and Lamin A

Danyang Yue¹, Yijuan Fan¹, Juan Lu¹, Mengxue Zhang¹, Jin Zhou¹, Yuying Bai¹, Jun Pan^1,*

1 Key Laboratory for Biorheological Science and Technology of Ministry of Education, State and Local Joint Engineering Laboratory for Vascular Implants, College of Bioengineering, Chongqing University, Chongqing, China.
* Corresponding Author: Jun Pan. Email: panj@cqu.edu.cn.

Molecular & Cellular Biomechanics 2019, 16(Suppl.2), 144-144. https://doi.org/10.32604/mcb.2019.07084

Abstract

Mesenchymal Stem Cells (MSCs) are recruited to the musculoskeletal system following trauma [1] or chemicals stimulation [2]. The regulation of their differentiation into either bone or cartilage cells is a key question. The fluid shear stress (FSS) is of pivotal importance to the development, function and even the repair of all tissues in the musculoskeletal system [3]. We previously found that MSCs are sensitive enough to distinguish a slight change of FSS stimulation during their differentiation commitment to bone or cartilage cells, and the internal mechanisms. In detail, MSCs were exposed to laminar FSS linearly increased from 0 to 10 dyn/cm² in 0, 2, or 20 min and maintained at 10 dyn/cm² for a total of 20 min (termed as ΔSS of 0-0', 0-2', and 0-20', respectively, representing more physiological (0-0') and non-physiological (0-2' and 0-20') ΔSS treatments). 0-0' facilitated MSC differentiation towards chondrogenic but not osteogenic phenotype. In contrast, 0-2' promoted MSCs towards osteogenic but not chondrogenic phenotype. 0-20' elicited the modest osteogenic and chondrogenic phenotypes [4]. In addition, we disclosed that 20 min of ΔSS could compete with 5 days' chemical and 2 days' substrate stiffness inductions, demonstrating ΔSS is potent regulator for MSC differentiation control [5]. We found that the ΔSS induced MSC differentiation into osteogenic or chondrogenic cells is directed through the modulation of cation-selective channels (MSCCs), intracellular calcium levels and F-actin. Here we demonstrate that the 0-2' induced significant lamin A; the 0-0' induced similar lamin A to 0-2' and 0-20' elicited less lamin A. A special ΔSS of 0-1' is found to induce osteogenic differentiation comparable to 0-2' and chondrogenic differentiation comparable to 0-0' as well as the most lamin A. Lamin A has no influence on the expression of runx2, a key transcription factor in osteogenic differentiation, but has affected the expression of sox9, a key transcription factor in chondrogenic differentiation. Our study presents evidences that the MSCs are highly sensitive to discriminate different ΔSS loads and differentiate towards the osteogenic or chondrogenic phenotype by regulating MSCCs and the subsequent [Ca²⁺]_i increase, F-actin assembly and Lamin A expression, which provides guidance for training osteoporosis and osteoarthritis patients and stresses the possible application in MSCs linage specification.

---

Keywords

---