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

机译:大鼠小肠绒毛和隐窝细胞分泌成分表达的本体变化。

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摘要

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.
机译:为了确定大鼠小肠在生长过程中分泌成分(SC)的合成中是否表现出定量变化,从出生到成年的间隔从空肠段分离出上皮绒毛和隐窝细胞。通过免疫放射测定法测量每个细胞级分中的SC浓度,并与蔗糖酶活性(分化的绒毛肠细胞的酶标记)进行比较。观察到以下结果。 (i)成年大鼠的SC浓度从隐窝(隐窝细胞中的平均浓度:636 +/- 173 ng / mg蛋白)到绒毛尖端(绒毛细胞中的平均浓度:152 +/- 17 ng)表现出特征性的浓度降低梯度/ mg蛋白)。该梯度与蔗糖酶活性的梯度相反。 (ii)在年轻的哺乳期(10天大)中,绒毛和隐窝细胞中都几乎不存在SC,但在断奶大鼠中其浓度逐渐升高,并在产后40天达到成年水平。 (iii)直到第20天的哺乳期中都没有出现SC隐窝到绒毛的细胞梯度,在产后第四个星期发育。 (iv)连续3天,用药理剂量的皮质酮或L-甲状腺素治疗10日龄的幼崽未能诱导空肠肠上皮细胞早熟合成,但浓度显着降低(P小于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内,未成熟隐窝细胞产生特异性受体以经上皮运输聚合免疫球蛋白的能力发生了重大变化。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)的成熟的饮食和激素变化不会触发这一个体发育过程的启动。

著录项

  • 期刊名称 Immunology
  • 作者

    J P Buts; D L Delacroix;

  • 作者单位
  • 年(卷),期 2019(54),1
  • 年度 2019
  • 页码 181–187
  • 总页数 7
  • 原文格式 PDF
  • 正文语种
  • 中图分类 免疫学;
  • 关键词

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