Okumura S, Mizoguchi T, Sato N, Yamaki M, Kobayashi Y, Yamauchi H, Ozawa H, Udagawa N, Takahashi N
Department of Biochemistry, Matsumoto Dental University, 1780 Hiro-oka Gobara, Shiojiri, Nagano 399-0781, Japan.
Bone. 2006 Oct;39(4):684-93. doi: 10.1016/j.bone.2006.04.010. Epub 2006 Jun 13.
Bone-resorbing osteoclasts form sealing zones and ruffled borders toward the bone surface. The sealing zone consists of a ring-like alignment of F-actin dots and surrounds the ruffled border, from which protons are secreted into the bone surface. Vacuolar-type proton ATPase (V-ATPase) in osteoclasts is a ruffled border-associated enzyme responsible for the proton secretion. We studied the interaction between microtubules and the actin cytoskeleton in osteoclasts. Confocal microscopic observation revealed that osteoclasts on glass coverslips, dentine slices and Osteologictrade mark discs formed the ring-like structure of F-actin dots, and microtubules overlapped the top of the F-actin dots. Osteoclasts cultured on dentine formed resorption pits within 48 h. The treatment of osteoclasts with cytochalasin D, an F-actin-depolymerizing reagent, induced perturbation of the microtubules in osteoclasts on glass and inhibited their pit-forming activity on dentine in a dose-dependent and reversible manner. Conversely, nocodazole, a microtubule-depolymerizing reagent, disrupted sealing zones and inhibited pit-forming activity of osteoclasts in a dose-dependent and reversible manner. V-ATPase showed a tendency to be localized inside sealing zones in osteoclasts. Treatment of osteoclasts with calcitonin induced both disruption of sealing zones and dispersion of V-ATPase to the whole area of the cytoplasm within 60 min. The microtubule networks in osteoclasts remained unchanged for 60 min even in the presence of calcitonin. These results suggest that coordination of the actin cytoskeleton and microtubules is important in the function of osteoclasts, but calcitonin selectively affects the actin cytoskeleton and induces the dispersion of V-ATPase without causing significant changes in the microtubules.
骨吸收破骨细胞朝向骨表面形成封闭区和褶皱缘。封闭区由F-肌动蛋白点的环状排列组成,围绕着褶皱缘,质子从褶皱缘分泌到骨表面。破骨细胞中的液泡型质子ATP酶(V-ATP酶)是一种与褶皱缘相关的酶,负责质子分泌。我们研究了破骨细胞中微管与肌动蛋白细胞骨架之间的相互作用。共聚焦显微镜观察显示,玻璃盖玻片、牙本质切片和Osteologic商标盘上的破骨细胞形成了F-肌动蛋白点的环状结构,微管与F-肌动蛋白点的顶部重叠。在牙本质上培养的破骨细胞在48小时内形成了吸收陷窝。用细胞松弛素D(一种F-肌动蛋白解聚试剂)处理破骨细胞,可诱导玻璃上破骨细胞中微管的紊乱,并以剂量依赖性和可逆的方式抑制其在牙本质上形成陷窝的活性。相反,诺考达唑(一种微管解聚试剂)以剂量依赖性和可逆的方式破坏封闭区并抑制破骨细胞的陷窝形成活性。V-ATP酶在破骨细胞的封闭区内有定位的趋势。用降钙素处理破骨细胞,在60分钟内可导致封闭区破坏和V-ATP酶分散到细胞质的整个区域。即使存在降钙素,破骨细胞中的微管网络在60分钟内仍保持不变。这些结果表明,肌动蛋白细胞骨架和微管的协调在破骨细胞的功能中很重要,但降钙素选择性地影响肌动蛋白细胞骨架并诱导V-ATP酶的分散,而不会引起微管的显著变化。