| Literature DB >> 33352987 |
Manuel Winter1, Petra Weissgerber1,2, Karolin Klein1, Femke Lux1,2, Daniela Yildiz1,3, Ulrich Wissenbach1, Stephan E Philipp1, Markus R Meyer1, Veit Flockerzi1, Claudia Fecher-Trost1.
Abstract
Calcium-selective transient receptor potential Vanilloid 6 (TRPV6) channels are expressed in fetal labyrinth trophoblasts as part of the feto-maternal barrier, necessary for sufficient calcium supply, embryo growth, and bone development during pregnancy. Recently, we have shown a less- compact labyrinth morphology of Trpv6-deficient placentae, and reduced Ca2+ uptake of primary trophoblasts upon functional deletion of TRPV6. Trpv6-/- trophoblasts show a distinct calcium-dependent phenotype. Deep proteomic profiling of wt and Trpv6-/- primary trophoblasts using label-free quantitative mass spectrometry leads to the identification of 2778 proteins. Among those, a group of proteases, including high-temperature requirement A serine peptidase 1 (HTRA1) and different granzymes are more abundantly expressed in Trpv6-/- trophoblast lysates, whereas the extracellular matrix protein fibronectin and the fibronectin-domain-containing protein 3A (FND3A) were markedly reduced. Trpv6-/-placenta lysates contain a higher intrinsic proteolytic activity increasing fibronectin degradation. Our results show that the extracellular matrix formation of the placental labyrinth depends on TRPV6; its deletion in trophoblasts correlates with the increased expression of proteases controlling the extracellular matrix in the labyrinth during pregnancy.Entities:
Keywords: FND3A; HTRA1; TRPV6; calcium homeostasis; extracellular matrix; fibronectin; granzyme; nano LC–MS/MS; placenta; trophoblast
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Year: 2020 PMID: 33352987 PMCID: PMC7767235 DOI: 10.3390/ijms21249674
Source DB: PubMed Journal: Int J Mol Sci ISSN: 1422-0067 Impact factor: 5.923