Heywood B R, Sparks N H, Shellis R P, Weiner S, Mann S
School of Chemistry, University of Bath, Claverton Down, UK.
Connect Tissue Res. 1990;25(2):103-19. doi: 10.3109/03008209009006985.
The morphology, structure and crystal growth of apatite crystals isolated from calcified turkey tendon and synthetic carbonated apatites have been examined using high resolution transmission electron microscopy. The biogenic apatite consisted of small (35 x 20 x 5 nm) platelike crystals. Despite their irregular shape and ill-defined edges, individual particles were single domain crystals. Lattice images recorded from isolated turkey tendon crystals indicated that the crystallographic c-axis (0001) of apatite lies in the plane of the plate and parallel to the length of the crystallites. Lattice images suggested that the top face corresponds to the (1100) face of carbonated apatite. Lattice fringes observed in platelike crystallites viewed from the side corresponded to the projection of the apatite structure viewed along the [1120] direction. Thus, it can be argued that crystal growth is constrained along the [1100] direction, extends laterally along the [1120] direction, and is maximal along the [0001] direction. This latter direction is aligned with the collagen fiber axis. A mean length to width ratio (1.7) was determined by systemically measuring the maximum distances parallel and perpendicular to the c-axis identified from lattice images of the crystals. Similar information was obtained from lattice images of crystals located in collagen fibres. This confirmed that the morphological and structural features of isolated turkey tendon apatite crystals correlate directly with the in vivo crystallochemical characteristics of apatite. Crystals of synthetic carbonated apatite prepared at 37 degrees C were also platelike and, although generally much larger, had length to width ratios comparable with the turkey tendon apatite. The synthetic carbonated apatites were noticeably more sensitive to radiolytic damage than the turkey tendon crystals. The crystallographic c-axis of the inorganic particles was aligned parallel with the long, physical axis of the plate and the top face was identified as (1100). Similar data were also obtained from noncarbonated synthetic apatite samples. The results of the present study offer critical information about the crystal growth of individual carbonated apatite crystals in calcified turkey tendon and its relationship to the morphology of the crystallites. As similar growth characteristics are expressed in synthetic analogues, the data bring into question the putative regulatory role of the collagen-based matrix upon the nucleation and growth of biogenic apatite.(ABSTRACT TRUNCATED AT 400 WORDS)
利用高分辨率透射电子显微镜对从钙化火鸡肌腱中分离出的磷灰石晶体以及合成碳酸磷灰石的形态、结构和晶体生长进行了研究。生物成因磷灰石由小的(35×20×5纳米)板状晶体组成。尽管其形状不规则且边缘不清晰,但单个颗粒为单畴晶体。从分离出的火鸡肌腱晶体记录的晶格图像表明,磷灰石的晶体学c轴(0001)位于板平面内且平行于微晶的长度。晶格图像表明顶面相当于碳酸磷灰石的(1100)面。从侧面观察板状微晶中观察到的晶格条纹对应于沿[1120]方向观察到的磷灰石结构投影。因此,可以认为晶体生长沿[1100]方向受到限制,沿[1120]方向横向延伸,且沿[0001]方向最大。后一个方向与胶原纤维轴对齐。通过系统测量从晶体晶格图像中识别出的平行和垂直于c轴的最大距离,确定了平均长宽比(1.7)。从位于胶原纤维中的晶体的晶格图像中获得了类似信息。这证实了分离出的火鸡肌腱磷灰石晶体的形态和结构特征与磷灰石的体内晶体化学特征直接相关。在37摄氏度下制备的合成碳酸磷灰石晶体也是板状的,尽管通常大得多,但其长宽比与火鸡肌腱磷灰石相当。合成碳酸磷灰石比火鸡肌腱晶体对辐射损伤明显更敏感。无机颗粒的晶体学c轴与板的长物理轴平行,顶面被确定为(1,1,0,0)。从非碳酸合成磷灰石样品中也获得了类似数据。本研究结果提供了关于钙化火鸡肌腱中单个碳酸磷灰石晶体的晶体生长及其与微晶形态关系的关键信息。由于合成类似物表现出相似的生长特性,这些数据对基于胶原的基质对生物成因磷灰石成核和生长的假定调节作用提出了质疑。(摘要截断于400字)