The channel-activating protease CAP1/Prss8 is required for placental labyrinth maturation

Hummler, Edith; Dousse, Aline; Rieder, Audrey; Stehle, Jean-Christophe; Rubera, Isabelle; Osterheld, Maria-Chiara; Beermann, Friedrich; Frateschi, Simona; Charles, Roch-Philippe (2013). The channel-activating protease CAP1/Prss8 is required for placental labyrinth maturation. PLoS ONE, 8(2), e55796. Public Library of Science 10.1371/journal.pone.0055796

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The serine protease CAP1/Prss8 is crucial for skin barrier function, lung alveolar fluid clearance and has been unveiled as diagnostic marker for specific cancer types. Here, we show that a constitutive knockout of CAP1/Prss8 leads to embryonic lethality. These embryos presented no specific defects, but it is during this period, and in particular at E13.5, that wildtype placentas show an increased expression of CAP1/Prss8, thus suggesting a placental defect in the knockout situation. The placentas of knockout embryos exhibited significantly reduced vascular development and incomplete cellular maturation. In contrary, epiblast-specific deletion of CAP1/Prss8 allowed development until birth. These CAP1/Prss8-deficient newborns presented abnormal epidermis, and died soon after birth due to impaired skin function. We thus conclude that a late placental insufficiency might be the primary cause of embryonic lethality in CAP1/Prss8 knockouts. This study highlights a novel and crucial role for CAP1/Prss8 in placental development and function.

Item Type:

Journal Article (Original Article)

Division/Institute:

04 Faculty of Medicine > Pre-clinic Human Medicine > Institute of Biochemistry and Molecular Medicine

UniBE Contributor:

Charles, Roch-Philippe

Subjects:

500 Science > 570 Life sciences; biology
600 Technology > 610 Medicine & health

ISSN:

1932-6203

Publisher:

Public Library of Science

Funders:

[UNSPECIFIED] SNF

Language:

English

Submitter:

Roch-Philippe Charles

Date Deposited:

10 Mar 2014 10:50

Last Modified:

05 Dec 2022 14:29

Publisher DOI:

10.1371/journal.pone.0055796

PubMed ID:

23405214

BORIS DOI:

10.7892/boris.43267

URI:

https://boris.unibe.ch/id/eprint/43267

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