Thiévent A, Connat J L
Anatomie et Physiologie Comparées, Université de Genève, Switzerland.
Cell Tissue Res. 1995 Jan;279(1):199-208. doi: 10.1007/BF00300704.
Immunohistochemistry of alpha-smooth muscle actin and desmin, two markers of smooth muscle cell differentiation, and electron-microscopic observation of thick filaments of myosin were performed on the media of the developing rat hepatic portal vein to gain insights into the chronology of differentiation of its longitudinal and circular smooth muscles. In accordance with the ultrastructural distribution of thin filaments, staining of alpha-smooth muscle actin is lightly positive in the myoblasts at postnatal day 1 and then extends in probably all muscle cells of the developing vessel. Desmin, which appears later than alpha-smooth muscle actin in the two muscles, is distributed throughout the longitudinal layer at day 8, whereas the first arrangements of thick filaments are detectable in most longitudinal muscle cells; at this stage, desmin and thick filaments are absent from the poorly differentiated circular muscle cells. The longitudinal muscle cells differentiate in a strikingly synchronized way from day 8 onwards, conferring a homogeneous structure to the developing and mature longitudinal layer. Several desmin-positive cells and a heterogeneous distribution of thick filaments occur in the circular muscle at day 14; the subsequent extension of these filaments in this layer results in a persisting heterogeneous distribution in the young 7-week-old adult. Many features of the mature smooth muscle cells are established within the third week in the longitudinal muscle, approximately one week before those of the circular layer. These results are consistent with the function of the longitudinal muscle as a spontaneously contractile smooth muscle unit, and emphasize the need for its fast maturation to fulfil its major role in the control of portal blood flow.
对发育中的大鼠肝门静脉中膜进行α-平滑肌肌动蛋白和结蛋白(平滑肌细胞分化的两个标志物)的免疫组织化学检测,以及肌球蛋白粗丝的电子显微镜观察,以深入了解其纵行和平滑肌环分化的时间顺序。根据细丝的超微结构分布,α-平滑肌肌动蛋白在出生后第1天的成肌细胞中染色呈弱阳性,然后可能在发育中血管的所有肌细胞中扩展。结蛋白在这两种肌肉中比α-平滑肌肌动蛋白出现得晚于,在第8天分布于整个纵行层,而在大多数纵行肌细胞中可检测到粗丝的首次排列;在此阶段,分化较差的环行肌细胞中没有结蛋白和粗丝。从第8天起,纵行肌细胞以惊人的同步方式分化,使发育中的和成熟的纵行层具有均匀的结构。在第14天,环行肌中有几个结蛋白阳性细胞和粗丝的不均匀分布;随后这些细丝在该层中的扩展导致在7周龄的年轻成体中持续存在不均匀分布。成熟平滑肌细胞的许多特征在纵行肌的第三周内形成,大约比环行层早一周。这些结果与纵行肌作为自发收缩的平滑肌单位的功能一致,并强调其快速成熟以在控制门静脉血流中发挥主要作用的必要性。