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大鼠小肠绒毛和隐窝细胞分泌成分表达的个体发育变化。

Ontogenic changes in secretory component expression by villous and crypt cells of rat small intestine.

作者信息

Buts J P, Delacroix D L

出版信息

Immunology. 1985 Jan;54(1):181-7.

Abstract

In order to determine whether the rat small intestine exhibits quantitative changes in the synthesis of the secretory component (SC) during growth, epithelial villus and crypt cells were isolated from jejunal segments at intervals after birth up to adulthood. SC concentration was measured in each cell fraction by immunoradiometric assay and compared to sucrase activity, an enzyme marker of the differentiated villus enterocyte. The following results were observed. (i) Adult rats showed a characteristic decreasing concentration gradient of SC from the crypts (mean concentration in crypt cells: 636 +/- 173 ng/mg protein) to the villus tip (mean concentration in villus cells: 152 +/- 17 ng/mg protein). This gradient was the reverse of that found for sucrase activity. (ii) In young sucklings (10 days old), SC was virtually absent in both villus and crypt cells, but its concentration progressively increased in weanling rats and reached adult levels by day 40 postpartum. (iii) The crypt to villus cell gradient of SC, absent in sucklings up to day 20, developed during the fourth postnatal week. (iv) Treatment of 10-day-old suckling pups with pharmacological doses of either corticosterone or L-thyroxine for 3 consecutive days failed to induce the precocious synthesis of SC by jejunal enterocytes, but produced significant (P less than 0.01) decreases in concentration. Under the same conditions, sucrase activity was markedly enhanced. In conclusion, major changes in the ability of the immature crypt cell to produce the specific receptor for transepithelial transport of polymeric immunoglobulins occur during the fourth week of rat life. The initiation of this ontogenic process is not triggered by the dietary and hormonal changes known to control the maturation of other functions linked to the differenciated villus cell, such as sucrase activity.

摘要

为了确定大鼠小肠在生长过程中分泌成分(SC)的合成是否出现定量变化,在出生后直至成年的不同时间间隔,从空肠段分离出上皮绒毛细胞和隐窝细胞。通过免疫放射分析测定每个细胞组分中的SC浓度,并与蔗糖酶活性(一种分化的绒毛肠上皮细胞的酶标志物)进行比较。观察到以下结果。(i)成年大鼠显示出SC从隐窝(隐窝细胞中的平均浓度:636±173 ng/mg蛋白质)到绒毛顶端(绒毛细胞中的平均浓度:152±17 ng/mg蛋白质)具有特征性的浓度递减梯度。这个梯度与蔗糖酶活性的梯度相反。(ii)在幼龄乳鼠(10日龄)中,绒毛和隐窝细胞中几乎都没有SC,但在断奶大鼠中其浓度逐渐增加,并在产后第40天达到成年水平。(iii)在出生后第20天之前的乳鼠中不存在SC的隐窝到绒毛细胞梯度,在出生后第四周形成。(iv)用药理剂量的皮质酮或L-甲状腺素连续3天处理10日龄的乳鼠,未能诱导空肠肠上皮细胞早熟合成SC,但导致浓度显著降低(P<0.01)。在相同条件下,蔗糖酶活性明显增强。总之,在大鼠生命的第四周,未成熟隐窝细胞产生聚合免疫球蛋白跨上皮转运特异性受体的能力发生了重大变化。这个个体发育过程的启动不是由已知控制与分化的绒毛细胞相关的其他功能(如蔗糖酶活性)成熟的饮食和激素变化触发的。

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