Extravillous trophoblast

Extravillous trophoblast or, abbreviated, EVT, are one form of differentiated trophoblast cells of the placenta. They are invasive mesenchymal cells which function to establish critical tissue connection in the developing placental-uterine interface. EVTs derive from progenitor cytotrophoblasts (CYT), as does the other main trophoblast subtype, syncytiotrophoblast (SYN).

EVTs that derive from CYT cells on the surface of placental villi that come into contact with the uterine wall - at the placental bed - begin to express the HLA-G antigen.[1] These interstitial subtype of EVTs then have the ability to invade and implant into the maternal decidua, where they anchor the developing placenta. The endovascular EVTs remodel maternal spiral arteries to control blood perfusion and oxygenation in the developing placenta.[2][3]

EVT are a low-incidence (<5% of trophoblasts), but critical and multifunctional, subtype of trophoblast in the placenta.

Function

As the placenta forms and the cytotrophoblast layer grows and extends, distal villous CYT differentiate to cell column CYT which eventually detach and invade deeply to the maternal decidua as interstitial EVTs.[4] These EVTs anchor placental villi to the maternal decidua. Shallow implantation of EVT is associated with poor placentation and preeclampsia. Endovascular EVTs are also major regulators of oxygenation during early placental development. Initially, they plug maternal spiral arteries to maintain hypoxia and prevent blood perfusion.[5][6] This protects the fetus and placenta from oxidative stress during early development in the histiotrophic (glandular nutrition) stage. As fetal nutrition switches to the hemotrophic (blood-derived nutrition) stage, EVT plugs dissolve and perfusion of maternal blood begins, allowing further development of both the fetus and placenta.[7][3]

Formation

Cells that will eventually become extraembryonic placental trophoblasts are derived from the trophectoderm. As the trophectoderm separates from the inner cell mass during blastulation, early trophoblasts begin to form the placenta.[8] Later in placental development, both interstitial and endovascular EVTs form as underlying progenitor cell column CYTs undergo epithelial to mesenchymal transition (EMT).[9] This cellular process continually occurs as the CYT layer replenishes extravillous trophoblasts. EMT of CYT to EVT in the placenta is strongly controlled by the transcription factor T-cell factor 4 (TCF4) which is Wnt-dependent.[10] Canonical Wnt signaling pathways have many downstream development-related transcription factor gene targets, including TCF4. Since developing placental trophoblasts do not necessarily follow canonical EMT, it has been suggested that a placental trophoblast-specific hybrid EMT is a separate iteration.[9]

Biological markers

Placental trophoblast subtypes can be distinguished by certain markers that are exclusive to each subtype. Transition from epithelial CYT to mesenchymal EVT can be tracked by a loss of E-cadherin and gain of N-cadherin. EVTs can also be distinguished by expression of human leukocyte antigen G (HLA-G), which is not expressed by other placental trophoblasts.[11] As other trophoblast subtypes in the placental are epithelial, mesenchymal markers like vimentin and fibronectin can also be used for identification. These markers, however, are not specific to EVT and can also stain stromal cells in the placenta.[11] As trophoblasts develop, they express different integrins. Whereas CYT can be identified by ITGA6, EVTs strongly express ITGA5.[12] The existing in vitro EVT models detailed below recapitulate these markers and staining to varying degrees of accuracy.

In vitro models

As EVTs are a critical cellular subtype of the placenta and their dysfunction is associated with a myriad of gestational illnesses,[13] they are an attractive topic for research. Acquisition of this primary cell type from sensitive tissues can be difficult and inconsistent. First and second trimester placental tissue must usually be obtained from elective abortions, a designation requiring more NIH documentation and oversight.[14] Tissue from term placentas is more readily available but cannot be used to address questions related to early development and dynamics. Dissociation of trophoblasts from other cell types in placental tissue can be procedurally difficult and pure trophoblast subtype populations take great lengths to obtain. Then, the resulting primary trophoblast cells can then only be kept in culture for a few days. Thus, there is a high demand for accurate cell lines to model primary placental trophoblasts. The immortalized cell line HTR-8/SVneo is commonly used to model EVTs. Newer multipotent trophoblast stem cell systems can be induced to differentiate into HLA-G+ EVT from CYT.[11] Systems of placental organoids can also grow invasive EVT when cultured in Matrigel.[15] Each of these options varies in their utility and accuracy to primary EVTs. As research groups continue to develop better techniques of recapitulating primary cells in vitro, proper modeling of placental EVTs remains a goal of the field.

References

  1. ↑ Moser, Gerit; Windsperger, Karin; Pollheimer, Jürgen; de Sousa Lopes, Susana Chuva; Huppertz, Berthold (1 October 2018). "Human trophoblast invasion: new and unexpected routes and functions". Histochemistry and Cell Biology. 150 (4): 361–370. doi:10.1007/s00418-018-1699-0. ISSN 1432-119X. PMC 6153604.
  2. ↑ Moser, Gerit; Weiss, Gregor; Sundl, Monika; Gauster, Martin; Siwetz, Monika; Lang-Olip, Ingrid; Huppertz, Berthold (1 March 2017). "Extravillous trophoblasts invade more than uterine arteries: evidence for the invasion of uterine veins". Histochemistry and Cell Biology. 147 (3): 353–366. doi:10.1007/s00418-016-1509-5. ISSN 1432-119X. PMC 5344955.
  3. 1 2 Pollheimer, Jürgen; Vondra, Sigrid; Baltayeva, Jennet; Beristain, Alexander Guillermo; Knöfler, Martin (13 November 2018). "Regulation of Placental Extravillous Trophoblasts by the Maternal Uterine Environment". Frontiers in Immunology. 9: 2597. doi:10.3389/fimmu.2018.02597. ISSN 1664-3224. PMC 6243063. PMID 30483261.
  4. ↑ Pijnenborg, R.; Bland, J.M.; Robertson, W.B.; Brosens, I. (October 1983). "Uteroplacental arterial changes related to interstitial trophoblast migration in early human pregnancy". Placenta. 4 (4): 397–413. doi:10.1016/S0143-4004(83)80043-5. PMID 6634666.
  5. ↑ Burton, Graham J.; Jauniaux, Eric; Charnock-Jones, D. Sephen (2010). "The influence of the intrauterine environment on human placental development". The International Journal of Developmental Biology. 54 (2–3): 303–312. doi:10.1387/ijdb.082764gb. ISSN 0214-6282. PMID 19757391.
  6. ↑ Brosens, I.; Robertson, W. B.; Dixon, H. G. (April 1967). "The physiological response of the vessels of the placental bed to normal pregnancy". The Journal of Pathology and Bacteriology. 93 (2): 569–579. doi:10.1002/path.1700930218. ISSN 0368-3494. PMID 6054057.
  7. ↑ Pijnenborg, R.; Dixon, G.; Robertson, W.B.; Brosens, I. (January 1980). "Trophoblastic invasion of human decidua from 8 to 18 weeks of pregnancy". Placenta. 1 (1): 3–19. doi:10.1016/S0143-4004(80)80012-9. PMID 7443635.
  8. ↑ Cockburn, Katie; Rossant, Janet (2010-04-01). "Making the blastocyst: lessons from the mouse". The Journal of Clinical Investigation. 120 (4): 995–1003. doi:10.1172/JCI41229. ISSN 0021-9738. PMC 2846056. PMID 20364097.
  9. 1 2 DaSilva-Arnold, Sonia; James, Joanna L.; Al-Khan, Abdulla; Zamudio, Stacy; Illsley, Nicholas P. (December 2015). "Differentiation of first trimester cytotrophoblast to extravillous trophoblast involves an epithelial–mesenchymal transition". Placenta. 36 (12): 1412–1418. doi:10.1016/j.placenta.2015.10.013. PMID 26545962.
  10. ↑ Meinhardt, Gudrun; Haider, Sandra; Haslinger, Peter; Proestling, Katharina; Fiala, Christian; Pollheimer, Jürgen; Knöfler, Martin (2014-05-01). "Wnt-Dependent T-Cell Factor-4 Controls Human Etravillous Trophoblast Motility". Endocrinology. 155 (5): 1908–1920. doi:10.1210/en.2013-2042. ISSN 0013-7227. PMID 24605829.
  11. 1 2 3 Okae, Hiroaki; Toh, Hidehiro; Sato, Tetsuya; Hiura, Hitoshi; Takahashi, Sota; Shirane, Kenjiro; Kabayama, Yuka; Suyama, Mikita; Sasaki, Hiroyuki; Arima, Takahiro (2018-01-04). "Derivation of Human Trophoblast Stem Cells". Cell Stem Cell. 22 (1): 50–63.e6. doi:10.1016/j.stem.2017.11.004. ISSN 1875-9777. PMID 29249463.
  12. ↑ Knöfler, Martin; Haider, Sandra; Saleh, Leila; Pollheimer, Jürgen; Gamage, Teena K. J. B.; James, Joanna (2019). "Human placenta and trophoblast development: key molecular mechanisms and model systems". Cellular and Molecular Life Sciences. 76 (18): 3479–3496. doi:10.1007/s00018-019-03104-6. ISSN 1420-682X. PMC 6697717. PMID 31049600.
  13. ↑ Khong, T. Y.; Wolf, F.; Robertson, W. B.; Brosens, I. (October 1986). "Inadequate maternal vascular response to placentation in pregnancies complicated by pre-eclampsia and by small-for-gestational age infants". BJOG: An International Journal of Obstetrics and Gynaecology. 93 (10): 1049–1059. doi:10.1111/j.1471-0528.1986.tb07830.x. ISSN 1470-0328. PMID 3790464. S2CID 72967416.
  14. ↑ "4.1.14 Human Fetal Tissue Research". grants.nih.gov. Retrieved 2021-03-23.
  15. ↑ Turco, Margherita Y.; Gardner, Lucy; Kay, Richard G.; Hamilton, Russell S.; Prater, Malwina; Hollinshead, Michael; McWhinnie, Alasdair; Esposito, Laura; Fernando, Ridma; Skelton, Helen; Reimann, Frank (2019-04-26). "Trophoblast organoids as a model for maternal-fetal interactions during human placentation". Nature. 564 (7735): 263–267. doi:10.1038/s41586-018-0753-3. ISSN 0028-0836. PMC 7220805. PMID 30487605.
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