Isolation and characterization of trophoblasts from enzymatic explants of human term placenta
In the present study, we describe a new method of isolation and culture of human villous and extravillous trophoblasts from term placenta. The cultivation of trypsinized placental villous tissue explants, followed by the isolation of cells from outgrowth islets allows for obtaining a cytotrophoblast...
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Published in | Human cell : official journal of Human Cell Research Society Vol. 30; no. 4; pp. 249 - 257 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
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Tokyo
Springer Japan
01.10.2017
Springer Nature B.V |
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Abstract | In the present study, we describe a new method of isolation and culture of human villous and extravillous trophoblasts from term placenta. The cultivation of trypsinized placental villous tissue explants, followed by the isolation of cells from outgrowth islets allows for obtaining a cytotrophoblast subpopulation that is free from contamination by other cell types. Compared to other methods, our protocol is mild, simple and effective, does not request costly reagents and provides isolation of the mononuclear cytotrophoblast cell populations free from contamination by other types of placental cells. The isolated cells proliferated and formed a pleomorphic monolayer, where cells fused into a small number of binuclear or polynuclear syncytiotrophoblasts. Isolated cytotrophoblast cells expressed the specific epithelial intermediate filament cytokeratin 7 (CK7), the epithelium-specific cell–cell adhesion molecule E-cadherin and were CD9-, CD45- and vimentin-negative. Cyto- and syncytiotrophoblasts obtained by this method can be used as a model or tool for the fundamental research of differentiation and function of human placental cells, and can provide a new understanding of drug distribution in placenta. Their combination with other in vitro cell models can be useful for studying a variety of other aspects concerning placental functions, which will provide new knowledge for understanding immunology, endocrinology and development of placenta. |
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AbstractList | In the present study, we describe a new method of isolation and culture of human villous and extravillous trophoblasts from term placenta. The cultivation of trypsinized placental villous tissue explants, followed by the isolation of cells from outgrowth islets allows for obtaining a cytotrophoblast subpopulation that is free from contamination by other cell types. Compared to other methods, our protocol is mild, simple and effective, does not request costly reagents and provides isolation of the mononuclear cytotrophoblast cell populations free from contamination by other types of placental cells. The isolated cells proliferated and formed a pleomorphic monolayer, where cells fused into a small number of binuclear or polynuclear syncytiotrophoblasts. Isolated cytotrophoblast cells expressed the specific epithelial intermediate filament cytokeratin 7 (CK7), the epithelium-specific cell-cell adhesion molecule E-cadherin and were CD9-, CD45- and vimentin-negative. Cyto- and syncytiotrophoblasts obtained by this method can be used as a model or tool for the fundamental research of differentiation and function of human placental cells, and can provide a new understanding of drug distribution in placenta. Their combination with other in vitro cell models can be useful for studying a variety of other aspects concerning placental functions, which will provide new knowledge for understanding immunology, endocrinology and development of placenta. |
Author | Poltavtseva, Rimma A. Kolokoltsova, Tamara D. Zurina, Irina M. Kosheleva, Nastasia V. Saburina, Irina N. Gorkun, Anastasia A. Repin, Vadim S. Sukhikh, Gennady T. |
Author_xml | – sequence: 1 givenname: Tamara D. surname: Kolokoltsova fullname: Kolokoltsova, Tamara D. organization: Laboratory of Cell Biology and Developmental Pathology, FSBSI “Institute of General Pathology and Pathophysiology”, FSBI “Research Center for Obstetrics, Gynecology and Perinatology” Ministry of Healthcare of the Russian Federation – sequence: 2 givenname: Irina N. surname: Saburina fullname: Saburina, Irina N. organization: Laboratory of Cell Biology and Developmental Pathology, FSBSI “Institute of General Pathology and Pathophysiology”, FSBEI FPE “Russian Medical Academy of Continuous Professional Education” of the Ministry of Healthcare of the Russian Federation – sequence: 3 givenname: Irina M. surname: Zurina fullname: Zurina, Irina M. email: izurina@gmail.com organization: Laboratory of Cell Biology and Developmental Pathology, FSBSI “Institute of General Pathology and Pathophysiology” – sequence: 4 givenname: Anastasia A. surname: Gorkun fullname: Gorkun, Anastasia A. organization: Laboratory of Cell Biology and Developmental Pathology, FSBSI “Institute of General Pathology and Pathophysiology” – sequence: 5 givenname: Nastasia V. surname: Kosheleva fullname: Kosheleva, Nastasia V. organization: Laboratory of Cell Biology and Developmental Pathology, FSBSI “Institute of General Pathology and Pathophysiology”, Faculty of Biology, Lomonosov Moscow State University – sequence: 6 givenname: Vadim S. surname: Repin fullname: Repin, Vadim S. organization: Laboratory of Cell Biology and Developmental Pathology, FSBSI “Institute of General Pathology and Pathophysiology”, FSBEI FPE “Russian Medical Academy of Continuous Professional Education” of the Ministry of Healthcare of the Russian Federation – sequence: 7 givenname: Rimma A. surname: Poltavtseva fullname: Poltavtseva, Rimma A. organization: FSBI “Research Center for Obstetrics, Gynecology and Perinatology” Ministry of Healthcare of the Russian Federation – sequence: 8 givenname: Gennady T. surname: Sukhikh fullname: Sukhikh, Gennady T. organization: FSBI “Research Center for Obstetrics, Gynecology and Perinatology” Ministry of Healthcare of the Russian Federation |
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CitedBy_id | crossref_primary_10_2478_acb_2022_0023 crossref_primary_10_1016_j_lfs_2020_118390 crossref_primary_10_1186_s13287_021_02192_1 crossref_primary_10_1016_j_xpro_2024_103179 crossref_primary_10_1016_j_placenta_2018_08_005 crossref_primary_10_3390_jpm13010022 crossref_primary_10_1016_j_lfs_2019_05_054 |
Cites_doi | 10.1016/0143-4004(94)90015-9 10.1530/JOE-12-0433 10.1016/0143-4004(92)90051-T 10.1210/er.2009-0001 10.1016/0143-4004(95)90100-0 10.1002/9781444393927.ch20 10.1016/S0143-4004(86)80160-6 10.1111/j.1600-0897.2008.00588.x 10.1016/j.biocel.2004.05.014 10.1210/en.2003-1241 10.1016/j.jim.2003.03.001 10.1016/j.placenta.2004.10.002 10.1016/j.ydbio.2008.07.017 10.1016/j.placenta.2010.11.023 10.1177/1933719110371853 10.1210/endo-118-4-1567 10.1053/plac.1999.0526 10.1053/plac.2002.0914 10.1007/s00441-012-1371-2 10.1111/j.1600-0897.2011.01006.x 10.1016/0022-1759(89)90405-5 10.1053/plac.2001.0644 10.1016/0143-4004(95)90080-2 10.1016/j.tcb.2010.08.002 10.1016/S0143-4004(05)80217-6 10.1128/CDLI.3.1.14-22.1996 10.1007/978-1-60327-009-0_4 |
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Keywords | Cell culture Cell isolation method Human term placenta Villous enzymatic explants Cytotrophoblast |
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Snippet | In the present study, we describe a new method of isolation and culture of human villous and extravillous trophoblasts from term placenta. The cultivation of... |
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SubjectTerms | Biomedical and Life Sciences Cadherins CD45 antigen CD9 antigen Cell adhesion & migration Cell adhesion molecules Cell Biology Cell culture Cell Culture Techniques - methods Cell Separation - methods Cells, Cultured Contamination Cytokeratin E-cadherin Endocrinology Epithelium Explants Female Gynecology Humans Keratin-7 Life Sciences Oncology Placenta Placenta - cytology Pregnancy Reproductive Medicine Research Article Stem Cells Surgery Trophoblasts Trophoblasts - cytology Trypsin Vimentin |
Title | Isolation and characterization of trophoblasts from enzymatic explants of human term placenta |
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