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大鼠肾脏的出生后发育,特别涉及近端小管的化学分化。

The postnatal development of the rat kidney, with special reference to the chemodifferentiation of the proximal tubule.

作者信息

Neiss W F, Klehn K L

出版信息

Histochemistry. 1981;73(2):251-68. doi: 10.1007/BF00493025.

Abstract

New nephron anlages appear in the renal cortex up to the 4th postnatal day (PD). The last anlages to be formed develop into functional nephrons by PD 10, and the cortex appears mature at PD 12 after formation of the cortex corticis. The renal medulla develops by the longitudinal growth of loops of Henle and collecting ducts. The immature medulla cannot be divided into different zones and corresponds structurally to the later inner stripe of the outer zone. The inner zone is formed by PD 8, and the outer stripe of the outer zone by PD 12. The renal medulla is mature at PD 21. From the start of its development, the renal proximal tubule consists of the pars convoluta and pars recta. In both parts the formation of the brush border is accompanied by the simultaneous appearance of brush border enzymes (alkaline phosphatase, gamma-glutamyltranspeptidase, dipeptidylaminopeptidase IV) and lysosomal enzymes (acid phosphatase, acid beta-galactosidase, N-acetylglucosaminidase, dipeptidylaminopeptidase II) over the full length of the proximal tubule. During the course of proximal tubule maturation, however, the lysosomal enzyme activities decline in the pass convoluta (with constant brush border enzyme activities), while the brush border enzyme activities increase in the pars recta (with constant lysosomal enzyme activities). The two parts further differ in that they exhibit different lysosomal patterns from the outset, the pars convoluta containing numerous large, highly enzyme-active lysosomes arranged in groups, and the pars recta containing only a few very small lysosomes with low enzyme activity. Thus, even in the newborn rat, the lysosomal pattern of the pars recta already corresponds to that of the mature S3 segment. The S1 and S2 segments of the pars convoluta first differentiate between PD 10 and 21, as the groups of large lysosomes are progressively broken up and the extent of the lysosomal apparatus is diminished, this proceeding in a retrograde direction from the end of the immature pars convoluta.

摘要

新的肾单位原基在出生后第4天(PD)之前出现在肾皮质。最后形成的原基在出生后第10天发育为功能性肾单位,在皮质形成后,出生后第12天皮质看起来成熟。肾髓质通过髓袢和集合管的纵向生长而发育。未成熟的髓质不能分为不同区域,在结构上对应于后来外带的内条纹。内带在出生后第8天形成,外带的外条纹在出生后第12天形成。肾髓质在出生后第21天成熟。从其发育开始,肾近端小管就由曲部和直部组成。在这两个部分中,刷状缘的形成伴随着刷状缘酶(碱性磷酸酶、γ-谷氨酰转肽酶、二肽基氨基肽酶IV)和溶酶体酶(酸性磷酸酶、酸性β-半乳糖苷酶、N-乙酰氨基葡萄糖苷酶、二肽基氨基肽酶II)在近端小管全长同步出现。然而,在近端小管成熟过程中,溶酶体酶活性在曲部下降(刷状缘酶活性恒定),而刷状缘酶活性在直部增加(溶酶体酶活性恒定)。这两个部分的进一步差异在于,它们从一开始就表现出不同的溶酶体模式,曲部含有许多成组排列的大的、高酶活性的溶酶体,而直部仅含有少数酶活性低的非常小的溶酶体。因此,即使在新生大鼠中,直部的溶酶体模式已经与成熟的S3段的模式相对应。曲部的S1和S2段在出生后第10天至21天之间首次分化出来,随着成组的大溶酶体逐渐分解,溶酶体装置的范围缩小,这一过程从未成熟曲部的末端开始逆向进行。

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