Use of Matrigel in culture affects cell phenotype and gene expression in the first trimester trophoblast cell line HTR8/SVneo

There is inconsistent use of Matrigel for experiments with the HTR8/SVneo first trimester trophoblast and other cell lines. We quantified the effects of Matrigel on the expression of genes considered to be markers of extravillous cytotrophoblast (EVT) differentiation and invasive potential. Culture...

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Published in:Placenta (Eastbourne) Vol. 33; no. 7; pp. 586 - 588
Main Authors: Highet, A.R., Zhang, V.J., Heinemann, G.K., Roberts, C.T.
Format: Journal Article
Language:English
Published: Kidlington Elsevier Ltd 01.07.2012
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ISSN:0143-4004, 1532-3102, 1532-3102
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Abstract There is inconsistent use of Matrigel for experiments with the HTR8/SVneo first trimester trophoblast and other cell lines. We quantified the effects of Matrigel on the expression of genes considered to be markers of extravillous cytotrophoblast (EVT) differentiation and invasive potential. Culture on Matrigel promoted formation of “endothelial-like” tubes and reduced mRNA expression of matrix metalloproteinase 2 (MMP2), cytokeratin 7 (KRT7) and integrin alpha 1 (ITGA1), while increasing VE-cadherin (CDH5) expression consistent with a vascular phenotype. This process may constitute part of the endothelial cell mimicry exhibited by endovascular EVTs invading the maternal spiral arteries. HTR8/SVneo appears to be phenotypically polymorphic and adopt endovascular morphology on Matrigel.
AbstractList There is inconsistent use of Matrigel for experiments with the HTR8/SVneo first trimester trophoblast and other cell lines. We quantified the effects of Matrigel on the expression of genes considered to be markers of extravillous cytotrophoblast (EVT) differentiation and invasive potential. Culture on Matrigel promoted formation of “endothelial-like” tubes and reduced mRNA expression of matrix metalloproteinase 2 (MMP2), cytokeratin 7 (KRT7) and integrin alpha 1 (ITGA1), while increasing VE-cadherin (CDH5) expression consistent with a vascular phenotype. This process may constitute part of the endothelial cell mimicry exhibited by endovascular EVTs invading the maternal spiral arteries. HTR8/SVneo appears to be phenotypically polymorphic and adopt endovascular morphology on Matrigel.
There is inconsistent use of Matrigel for experiments with the HTR8/SVneo first trimester trophoblast and other cell lines. We quantified the effects of Matrigel on the expression of genes considered to be markers of extravillous cytotrophoblast (EVT) differentiation and invasive potential. Culture on Matrigel promoted formation of "endothelial-like" tubes and reduced mRNA expression of matrix metalloproteinase 2 (MMP2), cytokeratin 7 (KRT7) and integrin alpha 1 (ITGA1), while increasing VE-cadherin (CDH5) expression consistent with a vascular phenotype. This process may constitute part of the endothelial cell mimicry exhibited by endovascular EVTs invading the maternal spiral arteries. HTR8/SVneo appears to be phenotypically polymorphic and adopt endovascular morphology on Matrigel.There is inconsistent use of Matrigel for experiments with the HTR8/SVneo first trimester trophoblast and other cell lines. We quantified the effects of Matrigel on the expression of genes considered to be markers of extravillous cytotrophoblast (EVT) differentiation and invasive potential. Culture on Matrigel promoted formation of "endothelial-like" tubes and reduced mRNA expression of matrix metalloproteinase 2 (MMP2), cytokeratin 7 (KRT7) and integrin alpha 1 (ITGA1), while increasing VE-cadherin (CDH5) expression consistent with a vascular phenotype. This process may constitute part of the endothelial cell mimicry exhibited by endovascular EVTs invading the maternal spiral arteries. HTR8/SVneo appears to be phenotypically polymorphic and adopt endovascular morphology on Matrigel.
AbstractThere is inconsistent use of Matrigel for experiments with the HTR8/SVneo first trimester trophoblast and other cell lines. We quantified the effects of Matrigel on the expression of genes considered to be markers of extravillous cytotrophoblast (EVT) differentiation and invasive potential. Culture on Matrigel promoted formation of “endothelial-like” tubes and reduced mRNA expression of matrix metalloproteinase 2 ( MMP2), cytokeratin 7 ( KRT7) and integrin alpha 1 ( ITGA1), while increasing VE-cadherin ( CDH5) expression consistent with a vascular phenotype. This process may constitute part of the endothelial cell mimicry exhibited by endovascular EVTs invading the maternal spiral arteries. HTR8/SVneo appears to be phenotypically polymorphic and adopt endovascular morphology on Matrigel.
Author Roberts, C.T.
Zhang, V.J.
Highet, A.R.
Heinemann, G.K.
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Issue 7
Keywords Gene expression
Trophoblast
Matrigel
Pregnancy
Trophoblaste
Cell culture
Vertebrata
Phenotype
Cell line
Mammalia
Fetal membrane
First trimester
In vitro
Language English
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Snippet There is inconsistent use of Matrigel for experiments with the HTR8/SVneo first trimester trophoblast and other cell lines. We quantified the effects of...
AbstractThere is inconsistent use of Matrigel for experiments with the HTR8/SVneo first trimester trophoblast and other cell lines. We quantified the effects...
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SubjectTerms Biological and medical sciences
Cell Differentiation - genetics
Cell Line
Collagen - administration & dosage
Collagen - pharmacology
Drug Combinations
Embryology: invertebrates and vertebrates. Teratology
Endothelial Cells - physiology
Fundamental and applied biological sciences. Psychology
Gene expression
Gene Expression - drug effects
Gestational Age
Humans
Integrin alpha1 - genetics
Internal Medicine
Keratins - genetics
Laminin - administration & dosage
Laminin - pharmacology
Matrigel
Matrix Metalloproteinase 2 - genetics
Obstetrics and Gynecology
Phenotype
Plastics
Proteoglycans - administration & dosage
Proteoglycans - pharmacology
Trophoblast
Trophoblasts - metabolism
Title Use of Matrigel in culture affects cell phenotype and gene expression in the first trimester trophoblast cell line HTR8/SVneo
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https://www.clinicalkey.es/playcontent/1-s2.0-S0143400412001452
https://dx.doi.org/10.1016/j.placenta.2012.04.003
https://www.ncbi.nlm.nih.gov/pubmed/22541610
https://www.proquest.com/docview/1015249009
Volume 33
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