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基底膜抗原在冷冻保存的早期胚胎心脏中的分布。

Distribution of basement membrane antigens in cryopreserved early embryonic hearts.

作者信息

Kitten G T, Markwald R R, Bolender D L

出版信息

Anat Rec. 1987 Apr;217(4):379-90. doi: 10.1002/ar.1092170409.

Abstract

The early embryonic heart is composed of two cylindrical epithelial layers, an inner endothelium and an outer myocardium. The cardiac jelly (CJ), an acellular accumulation of extracellular matrix (ECM), fills the space between the two epithelia. During development of the heart, a portion of the endothelial cells of the atrioventricular (AV) region differentiate into mesenchyme cells in a temporally and spacially specific manner. Although contiguous with those in the AV region, endothelial cells lining the ventricle never form mesenchyme in situ. At present, the mechanisms controlling the biphasic differentiation of the endothelium and the subsequent migration of cardiac mesenchymal cells are poorly understood. Although the CJ lies between two epithelial and is spatially equivalent to a basement membrane (BM), it has not traditionally been considered to be organized into a BM-like structure. The potential significance of this observation to developmental biology lies in the possibility that BM or their individual components (i.e., fibronectin (FN), laminin (LM), type IV collagen, and heparin sulfate proteoglycan (HSPG] may function as the regulatory site of epithelial differentiation and morphogenesis. A cryofixation technique was developed in order to determine the in situ immunohistochemical distribution of the BM components in the CJ. Results indicated that the CJ exists as the fusion between a larger myocardially derived BM having a lamina densa and an extended reticular lamina and an attenuated, endothelial-associated BM composed only of a lamina densa. Except for FN, the individual BM components were not all present during early stages, but instead appeared in a sequential manner, suggesting that all components of an adult-type BM are not required to initiate the assembly of a structural and functional BM during development. In the AV canal and outflow tract (OT), FN appeared as a progressively expanding gradient of material with the greatest density nearer the myocardium.

摘要

早期胚胎心脏由两个圆柱形上皮层组成,即内层的内皮和外层的心肌。心脏凝胶(CJ)是细胞外基质(ECM)的无细胞积聚,填充在两个上皮之间的空间。在心脏发育过程中,房室(AV)区域的一部分内皮细胞以时间和空间特异性的方式分化为间充质细胞。虽然与AV区域的内皮细胞相邻,但心室衬里的内皮细胞在原位从不形成间充质。目前,控制内皮细胞双相分化以及随后心脏间充质细胞迁移的机制尚不清楚。虽然CJ位于两个上皮之间,在空间上等同于基底膜(BM),但传统上它不被认为是组织成类似BM的结构。这一观察结果对发育生物学的潜在意义在于,BM或其单个成分(即纤连蛋白(FN)、层粘连蛋白(LM)、IV型胶原和硫酸乙酰肝素蛋白聚糖(HSPG))可能作为上皮分化和形态发生的调节位点。为了确定BM成分在CJ中的原位免疫组织化学分布,开发了一种冷冻固定技术。结果表明,CJ以融合形式存在,一侧是源自心肌的较大BM,具有致密层和延伸的网状层,另一侧是仅由致密层组成的变薄的、与内皮相关的BM。除了FN,单个BM成分在早期并非全部存在,而是依次出现,这表明在发育过程中启动结构和功能BM的组装并不需要成年型BM的所有成分。在房室管和流出道(OT)中,FN呈现为一种逐渐扩展的物质梯度,密度最大的部分靠近心肌。

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