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Natural Endogenous Human Matriptase and Prostasin Undergo Zymogen Activation via Independent Mechanisms in an Uncoupled Manner

The membrane-associated serine proteases matriptase and prostasin are believed to function in close partnership. Their zymogen activation has been reported to be tightly coupled, either as a matriptase-initiated proteolytic cascade or through a mutually dependent mechanism involving the formation of...

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Autores principales: Su, Hui Chen, Liang, Yan A., Lai, Ying-Jung J., Chiu, Yi-Lin, Barndt, Robert B., Shiao, Frank, Chang, Hsiang-Hua D., Lu, Dajun D., Huang, Nanxi, Tseng, Chun-Che, Wang, Jehng-Kang, Lee, Ming-Shyue, Johnson, Michael D., Huang, Shih-Ming, Lin, Chen-Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5148038/
https://www.ncbi.nlm.nih.gov/pubmed/27936035
http://dx.doi.org/10.1371/journal.pone.0167894
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author Su, Hui Chen
Liang, Yan A.
Lai, Ying-Jung J.
Chiu, Yi-Lin
Barndt, Robert B.
Shiao, Frank
Chang, Hsiang-Hua D.
Lu, Dajun D.
Huang, Nanxi
Tseng, Chun-Che
Wang, Jehng-Kang
Lee, Ming-Shyue
Johnson, Michael D.
Huang, Shih-Ming
Lin, Chen-Yong
author_facet Su, Hui Chen
Liang, Yan A.
Lai, Ying-Jung J.
Chiu, Yi-Lin
Barndt, Robert B.
Shiao, Frank
Chang, Hsiang-Hua D.
Lu, Dajun D.
Huang, Nanxi
Tseng, Chun-Che
Wang, Jehng-Kang
Lee, Ming-Shyue
Johnson, Michael D.
Huang, Shih-Ming
Lin, Chen-Yong
author_sort Su, Hui Chen
collection PubMed
description The membrane-associated serine proteases matriptase and prostasin are believed to function in close partnership. Their zymogen activation has been reported to be tightly coupled, either as a matriptase-initiated proteolytic cascade or through a mutually dependent mechanism involving the formation of a reciprocal zymogen activation complex. Here we show that this putative relationship may not apply in the context of human matriptase and prostasin. First, the tightly coupled proteolytic cascade between matriptase and prostasin might not occur when modest matriptase activation is induced by sphingosine 1-phospahte in human mammary epithelial cells. Second, prostasin is not required and/or involved in matriptase autoactivation because matriptase can undergo zymogen activation in cells that do not endogenously express prostasin. Third, matriptase is not required for and/or involved in prostasin activation, since activated prostasin can be detected in cells expressing no endogenous matriptase. Finally, matriptase and prostasin both undergo zymogen activation through an apparently un-coupled mechanism in cells endogenously expressing both proteases, such as in Caco-2 cells. In these human enterocytes, matriptase is detected primarily in the zymogen form and prostasin predominantly as the activated form, either in complexes with protease inhibitors or as the free active form. The negligible levels of prostasin zymogen with high levels of matriptase zymogen suggests that the reciprocal zymogen activation complex is likely not the mechanism for matriptase zymogen activation. Furthermore, high level prostasin activation still occurs in Caco-2 variants with reduced or absent matriptase expression, indicating that matriptase is not required and/or involved in prostasin zymogen activation. Collectively, these data suggest that any functional relationship between natural endogenous human matriptase and prostasin does not occur at the level of zymogen activation.
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spelling pubmed-51480382016-12-28 Natural Endogenous Human Matriptase and Prostasin Undergo Zymogen Activation via Independent Mechanisms in an Uncoupled Manner Su, Hui Chen Liang, Yan A. Lai, Ying-Jung J. Chiu, Yi-Lin Barndt, Robert B. Shiao, Frank Chang, Hsiang-Hua D. Lu, Dajun D. Huang, Nanxi Tseng, Chun-Che Wang, Jehng-Kang Lee, Ming-Shyue Johnson, Michael D. Huang, Shih-Ming Lin, Chen-Yong PLoS One Research Article The membrane-associated serine proteases matriptase and prostasin are believed to function in close partnership. Their zymogen activation has been reported to be tightly coupled, either as a matriptase-initiated proteolytic cascade or through a mutually dependent mechanism involving the formation of a reciprocal zymogen activation complex. Here we show that this putative relationship may not apply in the context of human matriptase and prostasin. First, the tightly coupled proteolytic cascade between matriptase and prostasin might not occur when modest matriptase activation is induced by sphingosine 1-phospahte in human mammary epithelial cells. Second, prostasin is not required and/or involved in matriptase autoactivation because matriptase can undergo zymogen activation in cells that do not endogenously express prostasin. Third, matriptase is not required for and/or involved in prostasin activation, since activated prostasin can be detected in cells expressing no endogenous matriptase. Finally, matriptase and prostasin both undergo zymogen activation through an apparently un-coupled mechanism in cells endogenously expressing both proteases, such as in Caco-2 cells. In these human enterocytes, matriptase is detected primarily in the zymogen form and prostasin predominantly as the activated form, either in complexes with protease inhibitors or as the free active form. The negligible levels of prostasin zymogen with high levels of matriptase zymogen suggests that the reciprocal zymogen activation complex is likely not the mechanism for matriptase zymogen activation. Furthermore, high level prostasin activation still occurs in Caco-2 variants with reduced or absent matriptase expression, indicating that matriptase is not required and/or involved in prostasin zymogen activation. Collectively, these data suggest that any functional relationship between natural endogenous human matriptase and prostasin does not occur at the level of zymogen activation. Public Library of Science 2016-12-09 /pmc/articles/PMC5148038/ /pubmed/27936035 http://dx.doi.org/10.1371/journal.pone.0167894 Text en © 2016 Su et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Su, Hui Chen
Liang, Yan A.
Lai, Ying-Jung J.
Chiu, Yi-Lin
Barndt, Robert B.
Shiao, Frank
Chang, Hsiang-Hua D.
Lu, Dajun D.
Huang, Nanxi
Tseng, Chun-Che
Wang, Jehng-Kang
Lee, Ming-Shyue
Johnson, Michael D.
Huang, Shih-Ming
Lin, Chen-Yong
Natural Endogenous Human Matriptase and Prostasin Undergo Zymogen Activation via Independent Mechanisms in an Uncoupled Manner
title Natural Endogenous Human Matriptase and Prostasin Undergo Zymogen Activation via Independent Mechanisms in an Uncoupled Manner
title_full Natural Endogenous Human Matriptase and Prostasin Undergo Zymogen Activation via Independent Mechanisms in an Uncoupled Manner
title_fullStr Natural Endogenous Human Matriptase and Prostasin Undergo Zymogen Activation via Independent Mechanisms in an Uncoupled Manner
title_full_unstemmed Natural Endogenous Human Matriptase and Prostasin Undergo Zymogen Activation via Independent Mechanisms in an Uncoupled Manner
title_short Natural Endogenous Human Matriptase and Prostasin Undergo Zymogen Activation via Independent Mechanisms in an Uncoupled Manner
title_sort natural endogenous human matriptase and prostasin undergo zymogen activation via independent mechanisms in an uncoupled manner
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5148038/
https://www.ncbi.nlm.nih.gov/pubmed/27936035
http://dx.doi.org/10.1371/journal.pone.0167894
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