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硬骨鱼壁层心包膜的超微结构

Ultrastructure of the parietal pericardium in teleosts.

作者信息

Leknes I L

出版信息

J Anat. 1984 Jun;138 ( Pt 4)(Pt 4):703-12.

PMID:6746406
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1164354/
Abstract

The ultrastructure of the parietal pericardium in Melanogrammus aeglefinus, Paracheirodon innesi, and Poecilia reticulata is described in larvae of variable age. This structure is composed of a mesothelial layer facing the pericardial cavity and an outer layer of collagen tissue. The latter is continuous with the surrounding tissue, i.e. mainly skeletal muscles. Generally, the parietal pericardium is attached to loose connective tissue dorsally, whereas its ventral and lateral parts are connected to muscles and tendons. Posteriorly, it is fused with the peritoneum. In prenatal larvae of P. reticulata the parietal pericardium is in contact with yolk material. The parietal mesothelial cells are attenuated and contain numerous ribosomes, a well developed Golgi apparatus, and a number of membrane-bound inclusion bodies (0.1-0.4 micron) of moderate electron density. In addition, numerous pinocytotic vesicles (80-100 nm) occur in differentiated mesothelial cells, whereas they are scarce in undifferentiated cells. Furthermore, bristle-coated vesicles are very rare in differentiated mesothelial cells, whereas they are seen regularly in undifferentiated cells. The collagen fibre bundles of the parietal pericardium are often orientated perpendicularly to each other, and in postnatal larvae of P. reticulata a one cell thick layer of melanophores occurs within the fibrous tissue. These cells contain numerous membrane-bound, highly electron-dense inclusion bodies (0.3-0.6 micron). They are occasionally seen in Paracheirodon innesi also, whereas they are absent in 2 and 6 days old larvae of M. aeglefinus and prenatal larvae of P. reticulata. Macrophages, capillaries, and nerve bundles occur in the pericardial and subpericardial connective tissue. The present results are discussed and compared with those previously reported for mammalian parietal pericardium.

摘要

描述了不同年龄阶段黑线鳕、宝莲灯鱼和孔雀鱼幼虫的心外膜超微结构。该结构由面向心包腔的间皮层和外层胶原组织组成。后者与周围组织连续,即主要是骨骼肌。一般来说,心外膜背侧附着于疏松结缔组织,而其腹侧和外侧部分与肌肉和肌腱相连。在后方,它与腹膜融合。在孔雀鱼产前幼虫中,心外膜与卵黄物质接触。心外膜间皮细胞变薄,含有大量核糖体、发育良好的高尔基体以及一些中等电子密度的膜结合包涵体(0.1 - 0.4微米)。此外,在分化的间皮细胞中出现大量胞饮小泡(80 - 100纳米),而在未分化细胞中则很少见。此外,有被小泡在分化的间皮细胞中非常罕见,而在未分化细胞中则经常可见。心外膜的胶原纤维束通常相互垂直排列,在孔雀鱼产后幼虫的纤维组织内有一层单细胞厚的黑素细胞。这些细胞含有大量膜结合的、高电子密度的包涵体(0.3 - 0.6微米)。在宝莲灯鱼中偶尔也能见到,而在黑线鳕2日龄和6日龄幼虫以及孔雀鱼产前幼虫中则不存在。巨噬细胞、毛细血管和神经束存在于心包和心包下结缔组织中。对目前的结果进行了讨论,并与先前报道的哺乳动物心外膜的结果进行了比较。

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本文引用的文献

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The use of lead citrate at high pH as an electron-opaque stain in electron microscopy.在电子显微镜检查中,将高pH值的柠檬酸铅用作电子不透明染色剂。
J Cell Biol. 1963 Apr;17(1):208-12. doi: 10.1083/jcb.17.1.208.
2
Histologic and ultrastructural features of normal human parietal pericardium.正常人体脏层心包的组织学和超微结构特征。
Am J Cardiol. 1980 Nov;46(5):744-53. doi: 10.1016/0002-9149(80)90424-5.
3
Ultrastructure of atrial endocardium and myocardium in three species of gadidae (Teleostei).三种鳕科鱼类(硬骨鱼纲)心房心内膜和心肌的超微结构
Cell Tissue Res. 1980;210(1):1-10. doi: 10.1007/BF00232136.
4
The innervation of the human foetal parietal pericardium.人类胎儿壁层心包的神经支配。
J Anat. 1970 Jan;106(Pt 1):181.
5
Electron microscopy of the skin of the teleost, Hippoglossoides elassodon.狭鳞庸鲽皮肤的电子显微镜检查
Z Zellforsch Mikrosk Anat. 1970;103(2):149-69. doi: 10.1007/BF00337309.
6
Cholinesterase-positive and catecholamine-containing nerves in the guinea-pig pericardium.豚鼠心包中的胆碱酯酶阳性和含儿茶酚胺神经。
Am J Anat. 1971 May;131(1):121-31. doi: 10.1002/aja.1001310108.
7
The normal pericardium.正常心包。
Am J Cardiol. 1970 Nov;26(5):455-65. doi: 10.1016/0002-9149(70)90702-2.
8
The ultrastructure of human and rat pericardium. II. Intercellular spaces and junctions.人和大鼠心包膜的超微结构。II. 细胞间隙和连接
Acta Pathol Microbiol Scand. 1967;71(4):547-63. doi: 10.1111/j.1699-0463.1967.tb05176.x.
9
The ultrastructure of human and rat pericardium. I. Parietal and visceral mesothelium.人和大鼠心包膜的超微结构。I. 壁层和脏层间皮。
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10
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