Regenerative Medicine Unit, Bambino Gesù Children's Hospital, Istituto di Ricovero e Cura a Carattere Scientifico, Rome, Italy.
Department of Biotechnological and Applied Clinical Sciences, University of L'Aquila, L'Aquila, Italy.
Arch Biochem Biophys. 2014 Sep 15;558:70-8. doi: 10.1016/j.abb.2014.06.017. Epub 2014 Jun 27.
Much has been written recently on osteoclast biology, but this cell type still astonishes scientists with its multifaceted functions and unique properties. The last three decades have seen a change in thinking about the osteoclast, from a cell with a single function, which just destroys the tissue it belongs to, to an "orchestrator" implicated in the concerted regulation of bone turnover. Osteoclasts have unique morphological features, organelle distribution and plasma membrane domain organization. They require polarization to cause extracellular bone breakdown and release of the digested bone matrix products into the circulation. Osteoclasts contribute to the control of skeletal growth and renewal. Alongside other organs, including kidney, gut, thyroid and parathyroid glands, they also affect calcemia and phosphatemia. Osteoclasts are very sensitive to pro-inflammatory stimuli, and studies in the '00s ascertained their tight link with the immune system, bringing about the question why bone needs a cell regulated by the immune system to remove the extracellular matrix components. Recently, osteoclasts have been demonstrated to contribute to the hematopoietic stem cell niche, controlling local calcium concentration and regulating the turnover of factors essential for hematopoietic stem cell mobilization. Finally, osteoclasts are important regulators of osteoblast activity and angiogenesis, both by releasing factors stored in the bone matrix, and secreting "clastokines" that regulate the activity of neighboring cells. All these facets will be discussed in this review article, with the aim of underscoring The Great Beauty of the osteoclast.
最近有很多关于破骨细胞生物学的文章,但这种细胞类型仍然以其多方面的功能和独特的特性令科学家们感到惊讶。在过去的三十年中,人们对破骨细胞的认识发生了变化,从一种只有单一功能的细胞(即只破坏其所属的组织)转变为一种“协调者”,参与骨转换的协同调节。破骨细胞具有独特的形态特征、细胞器分布和质膜域组织。它们需要极化才能引起细胞外骨破坏,并将消化的骨基质产物释放到循环中。破骨细胞有助于控制骨骼的生长和更新。与其他器官(包括肾脏、肠道、甲状腺和甲状旁腺)一起,它们还影响钙和磷的代谢。破骨细胞对促炎刺激非常敏感,00 年代的研究确定了它们与免疫系统的紧密联系,这就提出了一个问题,即为什么骨骼需要一个受免疫系统调节的细胞来去除细胞外基质成分。最近,破骨细胞被证明有助于造血干细胞龛,控制局部钙浓度并调节造血干细胞动员所必需的因子的周转率。最后,破骨细胞是成骨细胞活性和血管生成的重要调节剂,既可以通过释放储存在骨基质中的因子,也可以通过分泌“破骨细胞因子”来调节邻近细胞的活性。本文将讨论所有这些方面,旨在强调破骨细胞的“大美”。