The calcium transient characteristics induced by fluid shear stress affect the osteoblast proliferation

Copyright © 2017 Elsevier Inc. All rights reserved..

Ca2+ signaling is essential for bone metabolism. Fluid shear stress (FSS), which can induce a rapid release of calcium from endoplasmic reticulum (ER) to produce calcium transients, plays a significant role in osteoblast proliferation and differentiation. However, it is still unclear of how calcium transients induced by FSS activating a number of downstream signals which subsequently regulate cell functions. In this study, we performed a group of Ca2+ transients models, which were induced by FSS to investigate the effects of different magnitudes of Ca2+ transients in osteoblast proliferation. Further, we performed a global proteomic profile of MC3T3-E1 cells in different Ca2+ transients models stimulated by FSS. GO enrichment and KEGG pathway analysis revealed that the TCA cycle was activated in the proliferating process. The activation of TCA needed mitochondrial Ca2+ uptake which were influenced by the amplitude of Ca2+ transients induced by FSS. Our work elucidate that osteoblast proliferation induced by FSS was related to the magnitude of calcium transients, which further activated energetic metabolism signaling pathway. This work revealed further understanding the mechanism of osteoblast proliferation induced by mechanic loading and help us to design new methods for osteoporosis therapy.

Medienart:

E-Artikel

Erscheinungsjahr:

2018

Erschienen:

2018

Enthalten in:

Zur Gesamtaufnahme - volume:362

Enthalten in:

Experimental cell research - 362(2018), 1 vom: 01. Jan., Seite 51-62

Sprache:

Englisch

Beteiligte Personen:

Yu, Liyin [VerfasserIn]
Wang, Xiangmiao [VerfasserIn]
Gao, Xiaohang [VerfasserIn]
Tong, Jie [VerfasserIn]
Zhang, Jianbao [VerfasserIn]

Links:

Volltext

Themen:

Calcium
Calcium transients
Journal Article
Mitochondrial calcium uptake
Proteomic
Research Support, Non-U.S. Gov't
SY7Q814VUP
Shear stress
TCA cycle

Anmerkungen:

Date Completed 18.09.2018

Date Revised 18.09.2018

published: Print-Electronic

Citation Status MEDLINE

doi:

10.1016/j.yexcr.2017.11.001

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM277697964