首页> 美国卫生研究院文献>Journal of Bone and Mineral Research >Osteocytes Acidify their Microenvironment in response to PTHrP in vitro and in Lactating Mice in vivo
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Osteocytes Acidify their Microenvironment in response to PTHrP in vitro and in Lactating Mice in vivo

机译:体外和体内泌乳小鼠中成骨细胞酸化其微环境以响应PTHrP

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摘要

Osteocytes appear to mobilize calcium within minutes in response to PTH injections and we have previously shown that osteocytes remove their perilacunar matrix during lactation through activation of the PTH type 1 receptor. Mechanisms utilized by osteocytes to mobilize calcium are unknown but we hypothesized that the molecular components may be similar to those used by osteoclasts. Here we show, using IDG-SW3 cells that ATP6V0D2, an essential component of vacuolar ATPase in osteoclasts, and other genes associated with osteoclastic bone resorption increase with osteoblast to osteocyte differentiation. Furthermore, PTHrP increases ATP6V0D2 expression and induces proton generation by primary osteocytes, which is blocked by bafilomycin, a vacuolar ATPase inhibitor. These in vitro proton measurements raised the question of osteocyte viability in an acidic environment. Interestingly, osteocytes, showed enhanced viability at pH as low as 5 compared to osteoblasts and fibroblasts in vitro. To study in vivo acidification by osteocytes, virgin and lactating CD1 mice on a low calcium diet were injected with the pH indicator dye, acridine orange, and their osteocyte lacuno-canalicular system imaged by confocal microscopy. Lower pH was observed in lactating compared to virgin animals. In addition, a novel transgenic mouse line with a GFPtpz-tagged collagen α2(I) chain was used. Instead of the expected reduction in GFP-fluorescence only in the perilacunar matrix, reduced fluorescence was observed in the entire bone matrix of lactating mice. Based on our experiments showing quenching of GFP in vitro, we propose that the observed reduction in GFP fluorescence in lactating mice is due to quenching of GFP by the acidic pH generated by osteocytes. Together these findings provide novel mechanistic insight into how osteocytes remove calcium from their perilacunar/pericanalicular matrices through active acidification of their microenvironment and show that osteocytes, like osteoclasts, are resistant to the negative effects of acid on viability.
机译:响应PTH注射,成骨细胞似乎在几分钟之内就动员了钙,并且我们以前已经证明,骨细胞在哺乳期间通过激活PTH 1型受体来清除其腔周围基质。破骨细胞动员钙的机制尚不清楚,但我们假设分子成分可能与破骨细胞类似。在这里,我们显示,使用IDG-SW3细胞,破骨细胞中液泡ATPase的必需成分ATP6V0D2,以及与破骨细胞骨吸收相关的其他基因随着成骨细胞向成骨细胞的分化而增加。此外,PTHrP增加了ATP6V0D2的表达并诱导了初级骨细胞的质子生成,而初级骨细胞则被液泡ATPase抑制剂巴氟霉素所阻断。这些体外质子测量提出了在酸性环境中骨细胞生存力的问题。有趣的是,与成骨细胞和成纤维细胞相比,骨细胞在低至5的pH值下具有增强的生存能力。为了研究骨细胞的体内酸化作用,在低钙饮食下向处女和泌乳的CD1小鼠注射pH指示剂染料,a啶橙,并通过共聚焦显微镜对它们的骨细胞腔-小管系统进行成像。与原始动物相比,泌乳期的pH较低。另外,使用了具有GFPtpz标签的胶原α2(I)链的新型转基因小鼠系。代替仅在腔周围基质中预期的GFP荧光减少,在哺乳小鼠的整个骨基质中观察到荧光减少。根据我们的实验显示,GFP在体外淬灭,我们建议观察到的在哺乳期小鼠中GFP荧光的减少是由于骨细胞产生的酸性pH对GFP的淬灭。这些发现共同为破骨细胞如何通过其微环境的主动酸化从骨周/周皮基质中去除钙提供了新颖的力学见解,并表明破骨细胞像破骨细胞一样,能够抵抗酸对生存能力的负面影响。

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