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 Areolae1

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 contr...

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Veröffentlicht in:Biology of reproduction 2010-05, Vol.82 (5), p.854-864
Hauptverfasser: Song, Gwonhwa, Bailey, Daniel W, Dunlap, Kathrin A, Burghardt, Robert C, Spencer, Thomas E, Bazer, Fuller W, Johnson, Greg A
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container_end_page 864
container_issue 5
container_start_page 854
container_title Biology of reproduction
container_volume 82
creator Song, Gwonhwa
Bailey, Daniel W
Dunlap, Kathrin A
Burghardt, Robert C
Spencer, Thomas E
Bazer, Fuller W
Johnson, Greg A
description 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.
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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). 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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.</description><subject>cathepsins</subject><subject>cystatins</subject><subject>estradiol</subject><subject>gene regulation</subject><subject>pig</subject><subject>placenta</subject><subject>progesterone</subject><subject>proteases</subject><subject>uterus</subject><issn>0006-3363</issn><issn>1529-7268</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNqNUctOIzEQtBArEcJ-wkr-AAb8iOfBLYzCghRpIzacR_a4B4wce2SbQz6XP1lPAsp1L7arq6u65EboFyU3lDTiVhlvA4zB6wnfkJo0rDlDMypYU1SsrM_RjBBSFpyX_AJdxvhOCF1wxmfos5XpDcZoHL6_xiewvsbSadzuY5Ip4xbnI5N440NvHOCXBOEjHpo2VvbgkrzLZMoPIy1-9hbipFk57XeQQi7efjdmGnZegzXu9eCQ-x7sh9HF5k1GwNsgXRx9SNgPeBOyqXER_4U-QAKN1f4wfUqxGk0OZY3Eyz74GPFpxDKAtxLoFfoxSBvh59c9Ry8Pq237WKz__H5ql-tCMSGaQkpdsarivNI9LKqhhLpWWgulql4AVZINi0Y0dQ28ZKWg9aB4n78QmJBqoILPkTj6HoIEGLoxmJ0M-46SbtpTd9rThLvjnrKOH3WZ9g7-U_UP2vefGQ</recordid><startdate>201005</startdate><enddate>201005</enddate><creator>Song, Gwonhwa</creator><creator>Bailey, Daniel W</creator><creator>Dunlap, Kathrin A</creator><creator>Burghardt, Robert C</creator><creator>Spencer, Thomas E</creator><creator>Bazer, Fuller W</creator><creator>Johnson, Greg A</creator><general>Society for the Study of Reproduction, Inc</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>201005</creationdate><title>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 Areolae1</title><author>Song, Gwonhwa ; Bailey, Daniel W ; Dunlap, Kathrin A ; Burghardt, Robert C ; Spencer, Thomas E ; Bazer, Fuller W ; Johnson, Greg A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b2559-aad7277337dce47f6e88bdd5bb7c5e1ba2f495988e3626518fb3c323e25abf153</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>cathepsins</topic><topic>cystatins</topic><topic>estradiol</topic><topic>gene regulation</topic><topic>pig</topic><topic>placenta</topic><topic>progesterone</topic><topic>proteases</topic><topic>uterus</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Song, Gwonhwa</creatorcontrib><creatorcontrib>Bailey, Daniel W</creatorcontrib><creatorcontrib>Dunlap, Kathrin A</creatorcontrib><creatorcontrib>Burghardt, Robert C</creatorcontrib><creatorcontrib>Spencer, Thomas E</creatorcontrib><creatorcontrib>Bazer, Fuller W</creatorcontrib><creatorcontrib>Johnson, Greg A</creatorcontrib><collection>CrossRef</collection><jtitle>Biology of reproduction</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Song, Gwonhwa</au><au>Bailey, Daniel W</au><au>Dunlap, Kathrin A</au><au>Burghardt, Robert C</au><au>Spencer, Thomas E</au><au>Bazer, Fuller W</au><au>Johnson, Greg A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>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 Areolae1</atitle><jtitle>Biology of reproduction</jtitle><date>2010-05</date><risdate>2010</risdate><volume>82</volume><issue>5</issue><spage>854</spage><epage>864</epage><pages>854-864</pages><issn>0006-3363</issn><eissn>1529-7268</eissn><abstract>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). 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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). 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source BioOne Complete; Oxford University Press Journals All Titles (1996-Current); EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection
subjects cathepsins
cystatins
estradiol
gene regulation
pig
placenta
progesterone
proteases
uterus
title 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 Areolae1
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