Preview

Vestnik of North-Eastern Federal University. Medical Sciences

Advanced search

MORPHOLOGY OF PLACENTAL SYNCYTIOTROPHOBLAST IN DIFFERENT DATES OF NORMAL PREGNANCY

https://doi.org/10.25587/SVFU.2023.31.2.008

Abstract

The placenta is a fetal organ providing the interchange between mother and fetus. An important role in the regulation of local hemostasis belongs to the so-called brush border of syncytiotrophoblast villi, which is directly washed by maternal blood. Microvilli secrete placental alkaline phosphatase, which is a marker of transport processes and activates enzymes for many metabolic processes, participates in cell proliferation and tissue differentiation, carries out IgG transport to the fetus.
The purpose of the work is to characterize the development of syncytiotrophoblast of the epithelium of the placenta villi at different dates of gestation during physiological pregnancy. To achieve the goal of the study, the tasks were set:
1. Study the dynamics of villi branching and the structure of the trophoblastic epithelium of villi from the stage of branched chorion to the end of pregnancy.
2. Determine the area of the trophoblastic epithelium of villi and study the immunohistochemical features of its main components using antibodies placental alkaline phosphatase, β – chorionic gonadotropin. 3. Study the dynamics of structural transformations and secretory activity of cyto- and syncytiotrophoblast at different gestational dates.
Morphogenesis of syncytiotrophoblast of villous epithelium has been studied using histological, immunohistochemical and morphometric studies.
The morphology of microvilli has been traced throughout the gestation period. The first forming microvilli were detected by 5 weeks; by 7 weeks, they were taller and flask-shaped; 8 weeks – had a branching structure; 9 weeks – non-branching structure, large and cylindrical; by the end of pregnancy (39-40 weeks) – rare, and there were no microvilli in the area of syncytio-capillary membranes.
At 4-5 weeks, there is a weak degree of immunoexpression of β-hCG in the invasive cytotrophoblast and cytotrophoblastic epithelium and negative with the antibody against placental alkaline phosphatase. The area of the epithelium is 4,863.2 μm². At 6-7 weeks, the mean area of the villi is 19,705,5 μm². At 8-10 weeks, maximum epithelial area (6,370,7 μm²) and onset of placental alkaline phosphatase immunoexpression in the brush border area. In the period of 18-24 weeks, the area of villi decreases to 3,285,9 μm². At 39-40 weeks, terminal villi dominate with minimal values of the area of the trophoblastic epithelium, which is 786,2 μm². Syncytiocapillary membranes appear. A pronounced two-layer immunoexpression of placental alkaline phosphatase in the epithelium of all types of villi remains.

About the Authors

I. A. Zolotukhina
A.I. Evdokimov Moscow State University of Medicine and Dentistry, Ministry of Health of the Russian Federation
Russian Federation

ZOLOTUKHINA Irina Alekseevna – Candidate of Biological Sciences, Senior Lecturer, Department of Histology, Embryology, Cytology

Moscow, Russia, ul. Ivanteevskaya, d. 32, k. 2, kv. 34

8-964-572-64-38



N. V. Aleksandrovich
A.I. Evdokimov Moscow State University of Medicine and Dentistry, Ministry of Health of the Russian Federation
Russian Federation

ALEXANDROVICH Natalya Viktorovna – Candidate of Biological Sciences, Associate Professor, Department of Histology, Embryology and Cytology

Moscow, Russia, ul. Krasny Kazanets, 13, apt. 74

8-965-155-57-53



I. N. Dementeva
A.I. Evdokimov Moscow State University of Medicine and Dentistry, Ministry of Health of the Russian Federation
Russian Federation

DEMENTIEVA Irina Nikolaevna – Candidate of Medical Sciences, Associate Professor, Department of Histology, Embryology, Cytology

Moscow, Russia, ul. Krasny Kazanets, Troitsk, ul. Tekstilshchikov, 4, kv. 144

tel. 8-916-265-58-38



References

1. Liu Y, Fan X, Wang R, Lu X, Dang YL, Wang H, Lin HY, Zhu C, Ge H, Cross JC, Wang H. Single-cell RNA-seq reveals the diversity of trophoblast subtypes and patterns of differentiation in the human placenta. Cell Res. 2018; 28 :819–832. doi: 10.1038/s41422-018-0066-y.

2. Milovanov A.P. Citotrofoblasticheskaya invaziya – vazhnejshij mekhanizm placentacii i progressii beremennosti. Arhiv patologii. 2019; 81(4):-10.

3. McConkey C.A., Delorme-Axford E., Nickerson C.A., Kim K.S., Sadovsky Y., Boyle J.P., Coyne C.B. A three-dimensional culture system recapitulates placental syncytiotrophoblast development and microbial resistance. // Sci Adv. 2016. Mar; 2(3): e1501462.

4. Almasry S.M., Elfayomy A.K. Morphometric analysis of terminal villi and gross morphological changes in the placentae of term idiopathic intrauterine growth restriction. Tissue Cell. 2012. vol. 44. no. 4. P. 214-219.

5. Roland C.S., Hu J., Ren C.E., Chen H., Li J., Varvoutis M.S. Morphological changes of placental syncytium and their implications for the pathogenesis of preeclampsia. Cell. Mol. Life Sci.: CMLS. 2016;73(2):365–376.

6. Bronson SL, Bale TL. The placenta as a mediator of stress effects on neurodevelopmental reprogramming. Neuropsychopharmacology. 2016; 41:207–218.

7. Burton GJ, Jauniaux E. Development of the human placenta and fetal heart: synergic or independent? Front Physiol. 2018; 9: 373. doi: 10.3389/fphys.2018.00373.

8. Shchegolev A.I., Dubova E.A., Pavlov K.A., Lyapin V.M., Kulikova G.V., Shmakov R.G. Morfometricheskaya harakteristika terminal’nyh vorsin placenty pri preeklampsii // Byulleten’ eksperimental’noj biologii i mediciny – 2012.- № 7. – S. 104-107.

9. Gill J. S., SalafiaC. M., Grebenkov D., Vvedensky D. D. Modeling oxygene transport in human placental terminal villi. //Journal of Theoretical Biology. 2011. 12. 291, 33-41.

10. Guven D., Altunkaynak B.Z., Altun G., Alkan I., Kocak I. Histomorphometric changes in the placenta and umbilical cord during complications of pregnancy. Biotech Histochem. 2018. vol. 93. no. 3. P. 198-210.

11. Napso T, Yong HEJ, Lopez-Tello J, Sferruzzi-Perri AN. The role of placental hormones in mediating maternal adaptations to support pregnancy and lactation. Front Physiol. 2018; 9:1091.

12. Ptacek I., Smith A., Garrod A., Bullough S., Bradley N., Batra G., Sibley C.P., Jones R.L., Brownbill P., Heazell A.E. Quantitative assessment of placental morphology may identify specific causes of stillbirth. BMC Clin. Pathol. 2016. vol. 9. no. 16. P. 1.

13. Soares MJ, Iqbal K, Kozai K. Hypoxia and placental development. //Birth Defects Res. 2017. Oct 16;109(17):1309-1329.

14. Milovanov A.P., Erofeeva L.M., Aleksandrovich N.V., Zolotuhina I.A. Morfologiya placenty cheloveka vo II i III trimestrah beremennosti // Morfologiya. 2012. T.142, №5. S. 64-67.

15. Perepelica S.A., Golubev A.M., Smerdova E.F. Morfologiya placenty pri ochen’ rannih prezhdevremennyh rodah // Detskaya medicina Severo-Zapada. 2018. T. 7. № 1. S. 254-255.


Review

For citations:


Zolotukhina I.A., Aleksandrovich N.V., Dementeva I.N. MORPHOLOGY OF PLACENTAL SYNCYTIOTROPHOBLAST IN DIFFERENT DATES OF NORMAL PREGNANCY. Vestnik of North-Eastern Federal University. Medical Sciences. 2023;(2):67-74. (In Russ.) https://doi.org/10.25587/SVFU.2023.31.2.008

Views: 278


Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.


ISSN 2587-5590 (Online)