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碳酸酐酶II通过影响细胞内pH值和Ca2+的稳态,在破骨细胞分化和骨吸收中起主要作用。

Carbonic anhydrase II plays a major role in osteoclast differentiation and bone resorption by effecting the steady state intracellular pH and Ca2+.

作者信息

Lehenkari P, Hentunen T A, Laitala-Leinonen T, Tuukkanen J, Väänänen H K

机构信息

Department of Anatomy, University of Oulu, Finland.

出版信息

Exp Cell Res. 1998 Jul 10;242(1):128-37. doi: 10.1006/excr.1998.4071.

Abstract

Carbonic anhydrase II (CA II) expression in characteristic for the early stage of osteoclast differentiation. To study how CA II, which is crucial in proton generation in mature osteoclasts, influences the osteoclast differentiation process we performed rat bone marrow cultures. In this model, acetazolamide, a specific CA inhibitor, decreased the 1,25 (OH)2D3-induced formation of multinucleated tartrate-resistant acid phosphatase (TRAP)-positive cells, in a dose-dependent manner. We then performed intracellular pH (pHi) and Ca2+ (Cai2+) measurements for cultured osteoclasts and noticed that addition of acetazolamide caused a rapid, transient increase of both parameters. The increase in pHi was dependent neither on the culture substrate nor on the extracellular pH (pHe) but the increase could be diminished by DIDS or by bicarbonate removal. Membrane-impermeable CA inhibitors (benzolamide and pd5000) did not have this effect. Addition of CA II antisense oligonucleotides into the cultures reduced the pHi increase significantly. CA II inhibition was also found to neutralize the intracellular vesicles at extracellular pH (pHe) of 7.4, but at less extent at pHe 7.0. In mouse calvaria cultures, bone resorption was inhibited dose dependently by acetazolamide at pHe 7.4 while inhibition was smaller at pHe 7.0. We conclude that CA II is essential not only in bone resorption but also in osteoclast differentiation. In both processes, however, the crucial role of CA II is at least partially due to the effect on the osteoclast pHi regulation.

摘要

碳酸酐酶II(CA II)的表达是破骨细胞分化早期的特征。为了研究在成熟破骨细胞质子生成中起关键作用的CA II如何影响破骨细胞分化过程,我们进行了大鼠骨髓培养。在这个模型中,特异性CA抑制剂乙酰唑胺以剂量依赖的方式减少了1,25(OH)2D3诱导的抗酒石酸酸性磷酸酶(TRAP)阳性多核细胞的形成。然后我们对培养的破骨细胞进行了细胞内pH(pHi)和Ca2+(Cai2+)测量,发现添加乙酰唑胺会导致这两个参数迅速、短暂地增加。pHi的增加既不依赖于培养底物,也不依赖于细胞外pH(pHe),但DIDS或去除碳酸氢盐可减少这种增加。膜不可渗透的CA抑制剂(苯并酰胺和pd5000)没有这种作用。向培养物中添加CA II反义寡核苷酸可显著降低pHi的增加。还发现CA II抑制在细胞外pH(pHe)为7.4时可中和细胞内小泡,但在pHe为7.0时作用较小。在小鼠颅骨培养中,乙酰唑胺在pHe为7.4时剂量依赖性地抑制骨吸收,而在pHe为7.0时抑制作用较小。我们得出结论,CA II不仅在骨吸收中至关重要,在破骨细胞分化中也必不可少。然而,在这两个过程中,CA II的关键作用至少部分归因于对破骨细胞pHi调节的影响。

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