Abstract

We previously found that oscillatory fluid flow activated MC3T3-E1 osteoblastic cell Ca(2+)(i) mobilization via the inositol 1,4,5-trisphosphate pathway in the presence of 2% fetal bovine serum (FBS). However, the molecular mechanism of fluid flow-induced Ca(2+)(i) mobilization is unknown. In this study, we first demonstrated that oscillatory fluid flow in the absence of FBS failed to increase [Ca(2+)](i) in MC3T3-E1 cells. Apyrase (10 units/ml), which rapidly hydrolyzes 5' nucleotide triphosphates to monosphophates, prevented the fluid flow induced increases in [Ca(2+)](i) in the presence of FBS. Adding ATP or UTP to flow medium without FBS restored the ability of fluid flow to increase [Ca(2+)](i), suggesting that ATP or UTP may mediate the effect of fluid flow on [Ca(2+)](i). Furthermore, adenosine, ADP, UDP, or adenosine 5'-O-(3-thiotriphosphate) did not induce Ca(2+)(i) mobilization under oscillatory fluid flow without FBS. Pyridoxal phosphate 6-azophenyl-2,4'-disulfonic acid, an antagonist of P2X purinoceptors, did not alter the effect of fluid flow on the Ca(2+)(i) response, whereas pertussis toxin, a G(i/o)-protein inhibitor, inhibited fluid flow-induced increases in [Ca(2+)](i) in the presence of 2% FBS. Thus, by the process of elimination, our data suggest that P2Y purinoceptors (P2Y2 or P2Y4) are involved in the Ca(2+)(i) response to fluid flow. Finally, a decreased percentage of MC3T3-E1 osteoblastic cells treated with P2Y2 antisense oligodeoxynucleotides responded to fluid flow with an increase in [Ca(2+)](i), and an increased percentage of ROS 17/2.8 cells, which do not normally express P2Y2 purinoceptors, transfected with P2Y2 purinoceptors responded to fluid flow in the presence of 2% FBS, confirming that P2Y2 purinoceptors are responsible for oscillatory fluid flow-induced Ca(2+)(i) mobilization. Our findings shed new light of the molecular mechanisms responsible for oscillatory fluid flow-induced Ca(2+)(i) mobilization in osteoblastic cells.

Highlights

  • We previously found that oscillatory fluid flow activated MC3T3-E1 osteoblastic cell Ca2؉i mobilization via the inositol 1,4,5-trisphosphate pathway in the presence of 2% fetal bovine serum (FBS)

  • A decreased percentage of MC3T3-E1 osteoblastic cells treated with P2Y2 antisense oligodeoxynucleotides responded to fluid flow with an increase in [Ca2؉]i, and an increased percentage of ROS 17/2.8 cells, which do not normally express P2Y2 purinoceptors, transfected with P2Y2 purinoceptors responded to fluid flow in the presence of 2% FBS, confirming that P2Y2 purinoceptors are responsible for oscillatory fluid flow-induced Ca2؉i mobilization

  • In the presence of both 2% FBS and apyrase (10 units/ml), the percentage of cells responding with an increase in [Ca2ϩ]i was 3.91 Ϯ 1.62%, a value not significantly different from the percentage responding during the no flow period (2.64 Ϯ 1.98%) (p Ͼ 0.05)

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Summary

Introduction

We previously found that oscillatory fluid flow activated MC3T3-E1 osteoblastic cell Ca2؉i mobilization via the inositol 1,4,5-trisphosphate pathway in the presence of 2% fetal bovine serum (FBS). It is well known that mechanical loading of bone results in a variety of biophysical signals that may affect bone cellular metabolism and differentiation [1,2,3] One of these biophysical signals, extracellular fluid flow, has been demonstrated to be a potent stimulator of osteoblastic cell metabolic activity, differentiation, extracellular matrix protein production, and gene expression (4 – 8). We reported that oscillatory fluid flow in the presence of 2% fetal bovine serum (FBS), activated MC3T3-E1 osteoblastic cell intracellular calcium (Ca2ϩi) mobilization via the inositol 1,4,5-trisphosphate pathway and increased steady state levels of osteopontin, a bone extracellular matrix protein, mRNA in a Ca2ϩi-dependent manner [9]. Extracellular nucleotides are potential candidates responsible for fluid flow-induced Ca2ϩi mobilization in bone cells

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