Parfitt A M
Bone and Mineral Research Laboratory, Henry Ford Hospital, Detroit, Michigan 48202.
J Cell Biochem. 1994 Jul;55(3):273-86. doi: 10.1002/jcb.240550303.
The bone replacement process in the adult skeleton is known as remodeling. When bone is removed by osteoclasts, new bone is laid down by osteoblasts in the same place, because the load bearing requirement is unchanged. Bone is usually replaced because it is too old to carry out its function, which is mainly mechanical in cortical bone and mainly support for homeostasis and hematopoiesis in cancellous bone. Remodeling always begins on a quiescent bone surface, separated from the marrow by flat lining cells that are one of the two modes of terminal differentiation of osteoblasts. Lining cells are gatekeepers, able to be informed of the need for remodeling, and to either execute or mediate all four components of its activation-selection and preparation of the site, recruitment of mononuclear preosteoclasts, budding of new capillaries, and attraction of preosteoclasts to the chosen site where they fuse into multinucleated osteoclasts. In cortical bone, osteonal remodeling is carried out by a complex and unique structure, the basic multicellular unit (BMU) that comprises a cutting cone of osteoclasts in front, a closing cone lined by osteoblasts following behind, and connective tissue, blood vessels and nerves filling the cavity. The BMU maintains its size, shape and internal organization for many months as it travels through bone in a controlled direction. Individual osteoclast nuclei are short-lived, turning over about 8% per d, replaced by new preosteoclasts that originated in the bone marrow and travel in the circulation to the site of resorption. Refilling of bone at each successive cross-sectional location is accomplished by a team of osteoblasts, probably originating from precursors within the local connective tissue, all assembled within a narrow window of time, at the right location, and in the right orientation to the surface. Each osteoblast team forms bone most rapidly at its onset and slows down progressively. Some of the osteoblasts are buried as osteocytes, some die, and the remainder gradually assume the shape of lining cells. Cancellous bone is more accessible to study than cortical bone, but is geometrically complex. Although remodeling conforms to the same sequence of surface activation, resorption and formation, its three-dimensional organization is difficult to visualize from two-dimensional histologic sections.(ABSTRACT TRUNCATED AT 400 WORDS)
成人骨骼中的骨替换过程被称为重塑。当破骨细胞去除骨组织时,成骨细胞会在同一位置沉积新骨,因为承重需求未变。骨组织通常会被替换,是因为其过于陈旧而无法履行功能,在皮质骨中主要是机械功能,在松质骨中主要是维持内环境稳定和支持造血。重塑总是始于静止的骨表面,该表面与骨髓由扁平的衬里细胞分隔开,衬里细胞是成骨细胞终末分化的两种模式之一。衬里细胞是守门人,能够得知重塑的需求,并执行或介导其激活的所有四个组成部分——位点的选择和准备、单核前破骨细胞的募集、新毛细血管的出芽以及前破骨细胞被吸引到选定的位点并融合成多核破骨细胞。在皮质骨中,骨单位重塑由一种复杂而独特的结构——基本多细胞单位(BMU)进行,该单位包括前面的破骨细胞切割锥、后面有成骨细胞排列的封闭锥,以及填充腔隙的结缔组织、血管和神经。BMU在以可控方向穿过骨骼的过程中,会在数月内保持其大小、形状和内部结构。单个破骨细胞核寿命短暂,每天更新约8%,由源自骨髓并在循环中到达吸收部位的新前破骨细胞替代。在每个连续的横截面位置,骨组织的重新填充由一组成骨细胞完成,这些成骨细胞可能源自局部结缔组织内的前体细胞,它们在狭窄的时间窗口内,在正确的位置并以与表面正确的方向聚集在一起。每个成骨细胞团队在开始时形成骨的速度最快,随后逐渐减慢。一些成骨细胞会埋入成为骨细胞,一些会死亡,其余的逐渐呈现衬里细胞的形状。松质骨比皮质骨更容易进行研究,但在几何结构上较为复杂。尽管重塑遵循相同的表面激活、吸收和形成顺序,但其三维结构很难从二维组织学切片中直观呈现。(摘要截选至400字)