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Article ; Online: LIMK1 regulates human trophoblast invasion/differentiation and is down-regulated in preeclampsia.

Zhou, Yan / Yuge, Akitoshi / Rajah, Anthony M / Unek, Gozde / Rinaudo, Paolo F / Maltepe, Emin

The American journal of pathology

2014  Volume 184, Issue 12, Page(s) 3321–3331

Abstract: ... trophoblast stem cells as a discovery platform for human placentation disorders and suggest that LIMK1 ... secretion, invasion, and differentiation in vitro. Importantly, we also found that LIMK1 levels are ... differentiation by modulating the trophoblast cytoskeleton. Interestingly, in humans, LIMK1 activity promotes ...

Abstract Successful human pregnancy requires extensive invasion of maternal uterine tissues by the placenta. Invasive extravillous trophoblasts derived from cytotrophoblast progenitors remodel maternal arterioles to promote blood flow to the placenta. In the pregnancy complication preeclampsia, extravillous trophoblasts invasion and vessel remodeling are frequently impaired, likely contributing to fetal underperfusion and maternal hypertension. We recently demonstrated in mouse trophoblast stem cells that hypoxia-inducible factor-2 (HIF-2)-dependent Lim domain kinase 1 (LIMK1) expression regulates invasive trophoblast differentiation by modulating the trophoblast cytoskeleton. Interestingly, in humans, LIMK1 activity promotes tumor cell invasion by modulating actin and microtubule integrity, as well as by modulating matrix metalloprotease processing. Here, we tested whether HIF-2α and LIMK1 expression patterns suggested similar roles in the human placenta. We found that LIMK1 immunoreactivity mirrored HIF-2α in the human placenta in utero and that LIMK1 activity regulated human cytotrophoblast cytoskeletal integrity, matrix metallopeptidase-9 secretion, invasion, and differentiation in vitro. Importantly, we also found that LIMK1 levels are frequently diminished in the preeclampsia setting in vivo. Our results therefore validate the use of mouse trophoblast stem cells as a discovery platform for human placentation disorders and suggest that LIMK1 activity helps promote human placental development in utero.
MeSH term(s) Basic Helix-Loop-Helix Transcription Factors/metabolism ; Cell Differentiation ; Cell Movement ; Cytoskeleton/metabolism ; Down-Regulation ; Female ; Gene Expression Regulation, Developmental ; Humans ; Lim Kinases/metabolism ; Matrix Metalloproteinase 9/metabolism ; Microscopy, Fluorescence ; Placenta/metabolism ; Placentation ; Pre-Eclampsia/metabolism ; Pregnancy ; Pregnancy Trimester, Third ; Signal Transduction ; Stem Cells/cytology ; Trophoblasts/cytology ; Trophoblasts/metabolism
Chemical Substances Basic Helix-Loop-Helix Transcription Factors ; endothelial PAS domain-containing protein 1 (1B37H0967P) ; LIMK1 protein, human (EC 2.7.11.1) ; Lim Kinases (EC 2.7.11.1) ; MMP9 protein, human (EC 3.4.24.35) ; Matrix Metalloproteinase 9 (EC 3.4.24.35)
Language English
Publishing date 2014-10-13
Publishing country United States
Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
ZDB-ID 2943-9
ISSN 1525-2191 ; 0002-9440
ISSN (online) 1525-2191
ISSN 0002-9440
DOI 10.1016/j.ajpath.2014.08.013
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