CNN3 regulates trophoblast invasion and is upregulated by hypoxia in BeWo cells

CNN3 is an ubiquitously expressed F-actin binding protein, shown to regulate trophoblast fusion and hence seems to play a role in the placentation process. In this study we demonstrate that CNN3 levels are upregulated under low oxygen conditions in the trophoblast cell line BeWo. Since hypoxia is di...

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Veröffentlicht in:PloS one 2014-07, Vol.9 (7), p.e103216-e103216
Hauptverfasser: Appel, Sarah, Ankerne, Janina, Appel, Jan, Oberthuer, Andre, Mallmann, Peter, Dötsch, Jörg
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Ankerne, Janina
Appel, Jan
Oberthuer, Andre
Mallmann, Peter
Dötsch, Jörg
description CNN3 is an ubiquitously expressed F-actin binding protein, shown to regulate trophoblast fusion and hence seems to play a role in the placentation process. In this study we demonstrate that CNN3 levels are upregulated under low oxygen conditions in the trophoblast cell line BeWo. Since hypoxia is discussed to be a pro-migratory stimulus for placental cells, we examined if CNN3 is involved in trophoblast invasion. Indeed, when performing a matrigel invasion assay we were able to show that CNN3 promotes BeWo cell invasion. Moreover, CNN3 activates the MAPKs ERK1/2 and p38 in trophoblast cells and interestingly, both kinases are involved in BeWo invasion. However, when we repeated the experiments under hypoxic conditions, CNN3 did neither promote cell invasion nor MAPK activation. These results indicate that CNN3 promotes invasive processes by the stimulation of ERK1/2 and/or p38 under normoxic conditions in BeWo cells, but seems to have different functions at low oxygen levels. We further speculated that CNN3 expression might be altered in human placentas derived from pregnancies complicated by IUGR and preeclampsia, since these placental disorders have been described to go along with impaired trophoblast invasion. Our studies show that, at least in our set of placenta samples, CNN3 expression is neither deregulated in IUGR nor in preeclampsia. In summary, we identified CNN3 as a new pro-invasive protein in trophoblast cells that is induced under low oxygen conditions.
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In this study we demonstrate that CNN3 levels are upregulated under low oxygen conditions in the trophoblast cell line BeWo. Since hypoxia is discussed to be a pro-migratory stimulus for placental cells, we examined if CNN3 is involved in trophoblast invasion. Indeed, when performing a matrigel invasion assay we were able to show that CNN3 promotes BeWo cell invasion. Moreover, CNN3 activates the MAPKs ERK1/2 and p38 in trophoblast cells and interestingly, both kinases are involved in BeWo invasion. However, when we repeated the experiments under hypoxic conditions, CNN3 did neither promote cell invasion nor MAPK activation. These results indicate that CNN3 promotes invasive processes by the stimulation of ERK1/2 and/or p38 under normoxic conditions in BeWo cells, but seems to have different functions at low oxygen levels. We further speculated that CNN3 expression might be altered in human placentas derived from pregnancies complicated by IUGR and preeclampsia, since these placental disorders have been described to go along with impaired trophoblast invasion. Our studies show that, at least in our set of placenta samples, CNN3 expression is neither deregulated in IUGR nor in preeclampsia. 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In this study we demonstrate that CNN3 levels are upregulated under low oxygen conditions in the trophoblast cell line BeWo. Since hypoxia is discussed to be a pro-migratory stimulus for placental cells, we examined if CNN3 is involved in trophoblast invasion. Indeed, when performing a matrigel invasion assay we were able to show that CNN3 promotes BeWo cell invasion. Moreover, CNN3 activates the MAPKs ERK1/2 and p38 in trophoblast cells and interestingly, both kinases are involved in BeWo invasion. However, when we repeated the experiments under hypoxic conditions, CNN3 did neither promote cell invasion nor MAPK activation. These results indicate that CNN3 promotes invasive processes by the stimulation of ERK1/2 and/or p38 under normoxic conditions in BeWo cells, but seems to have different functions at low oxygen levels. We further speculated that CNN3 expression might be altered in human placentas derived from pregnancies complicated by IUGR and preeclampsia, since these placental disorders have been described to go along with impaired trophoblast invasion. Our studies show that, at least in our set of placenta samples, CNN3 expression is neither deregulated in IUGR nor in preeclampsia. In summary, we identified CNN3 as a new pro-invasive protein in trophoblast cells that is induced under low oxygen conditions.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>25050546</pmid><doi>10.1371/journal.pone.0103216</doi><oa>free_for_read</oa></addata></record>
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subjects Actin
Binding sites
Biology and life sciences
Calcium-Binding Proteins - genetics
Calcium-Binding Proteins - metabolism
Calponins
Cell activation
Cell adhesion & migration
Cell Line
Cell migration
Cell Movement
Deregulation
Enzyme Activation
Experiments
Extracellular signal-regulated kinase
Female
Gene expression
Gene Expression Regulation
Growth factors
Humans
Hypoxia
Hypoxia - metabolism
Kinases
MAP kinase
Matrix Metalloproteinase 14 - metabolism
Matrix Metalloproteinase 2 - metabolism
Medicine
Microfilament Proteins - genetics
Microfilament Proteins - metabolism
Mitogen-Activated Protein Kinase 1 - metabolism
Mitogen-Activated Protein Kinase 3 - metabolism
Muscle proteins
Oxygen
p38 Mitogen-Activated Protein Kinases - metabolism
Pediatrics
Phosphorylation
Placenta
Pre-eclampsia
Pre-Eclampsia - genetics
Pre-Eclampsia - metabolism
Pregnancy
Protein binding
Proteins
RNA, Messenger
Smooth muscle
Trophoblasts - cytology
Trophoblasts - metabolism
title CNN3 regulates trophoblast invasion and is upregulated by hypoxia in BeWo cells
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