首页> 外文期刊>Biology of Reproduction: Offical Journal of the Society for the Study of Reproduction >Cathepsin B, cathepsin L, and cystatin C in the porcine uterus and placenta: potential roles in endometrial/placental remodeling and in fluid-phase transport of proteins secreted by uterine epithelia across placental areolae.
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Cathepsin B, cathepsin L, and cystatin C in the porcine uterus and placenta: potential roles in endometrial/placental remodeling and in fluid-phase transport of proteins secreted by uterine epithelia across placental areolae.

机译:猪子宫和胎盘中的组织蛋白酶B,组织蛋白酶L和胱抑素C:在子宫内膜/胎盘重塑以及子宫上皮分泌的蛋白质跨胎盘乳晕的液相运输中的潜在作用。

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摘要

Cathepsins (CTSB and CTSL1) and their inhibitor, cystatin C (CST3), remodel uterine endometrium and placenta for transport of gases, micronutrients, and macromolecules essential for development and growth of the conceptus (embryo/fetus and placental membranes). We examined the temporal/spatial control of expression for CTSB, CTSL1, and CST3 mRNAs in endometria and placentae of pigs using three developmental models: 1) pigs were hysterectomized during the estrous cycle or pregnancy; 2) cyclic pigs were injected with estrogen to induce pseudopregnancy and were hysterectomized; and 3) pigs were ovariectomized, injected with progesterone, and hysterectomized. The abundance of CTSB, CTSL1, and CST3 mRNAs increased in endometrial epithelia during pregnancy and in response to exogenous progesterone but not estrogen. CST3 was also expressed in cells scattered within the stratum compactum stroma. Progesterone decreased epithelial but increased stromal compartment expression of CST3. CTSB increased in all chorionic epithelia, but CTSL1 was limited to chorionic epithelia that form areolae to absorb secretions from uterine glands. Based on the placental and endometrial distribution of CTSL1, we examined expression in the neonatal enterocytes known to transport immunoglobulins from colostrum. CTSL1 was also expressed in enterocytes of intestine from neonatal piglets. Therefore, CTSL1 is expressed by endometrial epithelia, placental areolae, and neonatal intestine, and it may function in the transport of macromolecules across these epithelia. Our results support the idea that reciprocal interactions between CSTL1, CTSB, and CST3 may be required to remodel endometrial and placental tissues for close apposition between maternal and fetal vasculatures and to facilitate transplacental transport of gases, micronutrients (amino acids, glucose), and macromolecules (proteins). Cysteine proteases and their inhibitors may also specifically modify proteins for successful utilization and fluid-phase transport across uterine, placental, and neonatal gut epithelia.
机译:组织蛋白酶(CTSB和CTSL1)及其抑制剂胱抑素C(CST3)可重塑子宫内膜和胎盘,以运输对概念发育和增长至关重要的气体,微量营养素和大分子(胚胎/胎儿和胎盘膜)。我们使用三种发育模型检查了猪子宫内膜和胎盘中CTSB,CTSL1和CST3 mRNA表达的时空控制:1)在发情周期或妊娠期间对猪进行了子宫切除术。 2)给周期性猪注射雌激素以诱导假孕并进行子宫切除术。 3)将猪切除卵巢,注射黄体酮并进行子宫切除。妊娠期间,子宫内膜上皮细胞中CTSB,CTSL1和CST3 mRNA的丰度增加,并且响应于外源孕激素而不是雌激素。 CST3也在致密层间质中的细胞中表达。孕酮减少上皮但增加CST3的基质区室表达。 CTSB在所有绒毛膜上皮中均增加,但CTSL1限于形成乳晕以吸收子宫腺分泌物的绒毛膜上皮。基于CTSL1的胎盘和子宫内膜分布,我们检查了已知从初乳转运免疫球蛋白的新生儿肠上皮细胞中的表达。 CTSL1也在新生仔猪的肠肠上皮细胞中表达。因此,CTSL1在子宫内膜上皮,胎盘乳晕和新生儿肠道中表达,并且可能在大分子穿过这些上皮的运输中发挥作用。我们的结果支持以下观点:可能需要CSTL1,CTSB和CST3之间的相互相互作用来重塑子宫内膜和胎盘组织,以紧密结合母体和胎儿脉管,并促进胎盘中气体,微量营养素(氨基酸,葡萄糖)和大分子的转运(蛋白质)。半胱氨酸蛋白酶及其抑制剂也可以特异性修饰蛋白质,以成功利用它们并在子宫,胎盘和新生儿肠道上皮细胞中进行液相运输。

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