Center for Animal Biotechnology & Genomics, Department of Veterinary Integrative Biosciences, and Department of Animal Science, Texas A&M University, College Station, Texas 77843-2471, USA.
Biol Reprod. 2010 May;82(5):854-64. doi: 10.1095/biolreprod.109.080929. Epub 2010 Jan 27.
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.
组织蛋白酶(CTSB 和 CTSL1)及其抑制剂胱抑素 C(CST3)重塑子宫子宫内膜和胎盘,以运输气体、微量营养素和大分子,这些物质对胚胎(胚胎/胎儿和胎盘膜)的发育和生长至关重要。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 的时空表达控制:1)在发情周期或怀孕期间对猪进行子宫切除术;2)给发情周期的猪注射雌激素以诱导假妊娠并进行子宫切除术;3)对猪进行卵巢切除术,注射孕酮并进行子宫切除术。CTSB、CTSL1 和 CST3 mRNA 的丰度在怀孕期间和对外源性孕酮而不是雌激素的反应中增加了子宫内膜上皮。CST3 也在致密层基质中的分散细胞中表达。孕酮减少了上皮细胞,但增加了 CST3 的基质隔室表达。CTSB 在所有绒毛膜上皮中增加,但 CTSL1 仅限于形成乳晕以吸收来自子宫腺分泌物的绒毛膜上皮。基于胎盘和子宫内膜中 CTSL1 的分布,我们检查了已知从初乳中转运免疫球蛋白的新生儿肠上皮细胞中的表达。CTSL1 也在新生仔猪的肠内细胞中表达。因此,CTSL1 由子宫内膜上皮、胎盘乳晕和新生儿肠表达,它可能在这些上皮细胞中运输大分子的功能。我们的结果支持这样的观点,即 CSTL1、CTSB 和 CST3 之间的相互作用可能是重塑子宫内膜和胎盘组织所必需的,以实现母体和胎儿血管之间的紧密贴合,并促进气体、微量营养素(氨基酸、葡萄糖)和大分子(蛋白质)的胎盘转运。半胱氨酸蛋白酶及其抑制剂也可能专门修饰蛋白质,以成功利用和通过子宫、胎盘和新生儿肠道上皮的液相传质。