Preview

Yakut Medical Journal

Advanced search

Signaling functions of fatty acids in the placenta

https://doi.org/10.25789/YMJ.2021.73.25

Abstract

This review summarizes the current understanding of FA-activated signal transduction systems in the placenta in the data PubMed, Google Scholar. Their effect on membrane and nuclear receptors, as well as their participation in the processes of decidualization and modulation of inflammation in the placenta, associated with G-protein-coupled receptors, have been shown. The effects of peroxisome proliferator-activated receptors mediated FAs in the placenta are described. Particular attention is paid to the Toll-mediated inflammatory signaling pathways of the FAs in the placenta. Research data on the effect of FAs on the expression of genes involved in placenta angiogenesis are summarized.

About the Authors

N. A. Ishutina
Far Eastern Scientific Center of Physiology and Pathology of Respiration
Russian Federation

Ishutina Nataliа A. – PhD, D.Sc. (Biol.), Leading Staff Scientist of Laboratory of Mechanisms of Etiopathogenesis and Recovery Processes of the Respiratory System at NonSpecific Lung Diseases

22 Kalinina Str., Blagoveshchensk, 675000



I. A. Andrievskaya
Far Eastern Scientific Center of Physiology and Pathology of Respiration
Russian Federation

Andrievskaya Irina A. – PhD, D.Sc. (Biol.), Professor RANS, Head of Laboratory of Mechanisms of Etiopathogenesis and Recovery Processes of the Respiratory System at Non-Specific Lung Diseases

22 Kalinina Str., Blagoveshchensk, 675000



M. N. German
Far Eastern Scientific Center of Physiology and Pathology of Respiration
Russian Federation

German Marina N. – Research Assistant at the Laboratory of Mechanisms of Etiopathogenesis and Recovery Processes of the Respiratory System at Non-Specific Lung Diseases

22 Kalinina Str., Blagoveshchensk, 675000



References

1. Effect of Oxidative Stress and Fatty Acids Disbalance on the Development of Apoptosis in the Placenta with Cytomegalovirus Infection in the First Trimester / N.A. Ishutina, I.A. Andrievskaya, I.V. Dovzhikova [et al.] // Acta Biomedica Scientifica. – 2019. – Vol. 4, №2. – 16-22. doi: 10.29413/ABS.2019-4.2.2.

2. Ishutina N.A. The role of Pamitic acid in implementation of apoptosis in cytomegalovirus infection in the gestation period / N.A. Ishutina, M.T. Lutsenko, N.N. Dorofienko // Siberian Medical Journal (Irkutsk). – 2017. – №1. – P. 11-14.

3. The role of innate immunity receptors (TLRs) in maintaining the homeostasis of the female genital tract in developing pregnancy and intrauterine infection / A.V. Karaulov, S.S. Afanasiev, V.A. Aleshkin [et al.] // Russian Journal of Infection and Immunity. – 2018. – Vol. 8, №3. – P. 251-262. doi:10.15789/2220-7619-2018-3-251-262.

4. A novel antiinflammatory role for the shortchain fatty acids in human labor / C. Voltolini, S. Battersby, S.L. Etherington [et al.] // Endocrinology. – 2012. – Vol. 153, №1. – P. 395-403. doi:10.1210/en.2011-1457.

5. Basak S. Fatty acid-induced angiogenesis in first trimester placental trophoblast cells: possible roles of cellular fatty acid-binding proteins / S. Basak, M.K. Das, A.K. Duttaroy // Life Sci. – 2013. –Vol. 93, №21. – P.755-762. doi:10.1016/j.lfs.2013.09.024.

6. Basak S. Cis-9, trans-11 conjugated linoleic acid stimulates expression of angiopoietin like4 in the placental extravillous trophoblast cells / S. Basak, A.K. Duttaroy // Biochim. Biophys. Acta. – 2013. – Vol. 1831, №4. – P. 834-843. doi:10.1016/j.bbalip.2013.01.012.

7. Basak S. Effects of fatty acids on angiogenic activity in the placental extravillious trophoblast cells / S. Basak, A.K. Duttaroy // Prostaglandins Leukot. Essent. Fatty Acids. – 2013. –Vol. 88, №2. – P. 155-162. doi:10.1016/j.plefa.2012.10.001.

8. CD36 Mediated Fatty Acid-Induced Podocyte Apoptosis via Oxidative Stress / W. Hua, H.Z. Huang, L.T. Tan [et al.] // PLoS One. – 2015. – Vol. 22, № 10(5). – e0127507. doi: 10.1371/journal.pone.0127507.

9. Cellular growth and tube formation of HTR8/SVneo trophoblast: effects of exogenously added fatty acid-binding protein-4 and its inhibitor / S. Basak, A. Sarkar, S. Mathapat [et al.] // Mol. Cell. Biochem. – 2018. –Vol. 437, №1-2. – P. 55-64. doi:10.1007/s11010-017-3095-9.

10. Docosahexaenoic acid inhibits vascular endothelial growth factor (VEGF)-induced cell migration via the GPR120/PP2A/ERK1/2/eNOS signaling pathway in human umbilical vein endothelial cells / C.Y. Chao, C.K. Lii, S.Y. Ye [et al.] // J. Agric. Food. Chem. – 2014. – Vol. 62, №18. – P. 4152-4158. doi:10.1021/jf5007165.

11. Docosahexaenoic acid stimulates tube formation in first trimester trophoblast cells, HTR8/SVneo / G.M. Johnsen, S. Basak, M.S. Weedon-Fekjær [et al.] // Placenta. – 2011. – Vol. 32, №9. – P. 626-632. doi:10.1016/j.placenta.2011.06.009.

12. Effect of α-linolenic acid on endoplasmic reticulum stress-mediated apoptosis of palmitic acid lipotoxicity in primary rat hepatocytes / Y. Zhang, X. Yang, H. Shi [et al.] // Lipids Health Dis. – 2011. – №10:P. 122-127. doi: 10.1186/1476-511X-10-122.

13. Expression and localization of the omega-3 fatty acid receptor GPR120 in human term placenta / S. Lager, V.I. Ramirez, F. Gaccioli [et al.] // Placenta. – 2014. – Vol. 35, №7. – P. 523-525. doi:10.1016/j.placenta.2014.04.017.

14. Fatty acids modulate Toll-like receptor 4 activation through regulation of receptor dimerization and recruitment into lipid rafts in a reactive oxygen species-dependent manner / S.W. Wong, M.J. Kwon, A.M. Choi [et al.] // J. Biol. Chem. – 2009. – Vol. 284, №40. – P. 27384-27392. doi:10.1074/jbc.M109.044065.

15. Free fatty acids regulate gut incretin glucagon-like peptide-1 secretion through GPR120 / A. Hirasawa, K. Tsumaya, T. Awaji [et al.] // Nat. Med. – 2005. – Vol. 11, №1. – P. 90-94. doi: 10.1038/nm1168.

16. Jadoon A. Regulation of fatty acid binding proteins by hypoxia inducible factors 1α and 2α in the placenta: relevance to preeclampsia / A. Jadoon, P. Cunningham, L.C. McDermott // Prostaglandins Leukot. Essent. Fatty Acids. – 2015. – №93. – P. 25-29. doi:10.1016/j.pleЖК.2014.09.004.

17. Koga K. Toll-like receptors at the maternal-fetal interface in normal pregnancy and pregnancy disorders / K. Koga, G. Mor // Am. J. Reprod. Immunol. – 2010. – Vol. 63, №6. – P. 587-600. doi:10.1111/j.1600-0897.2010.00848.x.

18. Lager S. Oleic acid stimulates system A amino acid transport in primary human trophoblast cells mediated by tolllike receptor 4 / S. Lager , F. Gaccioli, V.I. Ramirez // J. Lipid. Res. – 2013. – Vol. 54, №3. – P. 725-733. doi:10.1194/jlr.M033050.

19. Lager S. Differential regulation of placental amino acid transport by saturated and unsaturated fatty acids / S. Lager, T. Jansson, T.L. Powell // Am. J. Physiol. Cell. Physiol. – 2014. – Vol. 307, №8. – P. 738-C744. doi:10.1152/ajpcell.00196.2014.

20. LPS enhances TLR4 expression and IFN γ production via the TLR4/IRAK/NF κB signaling pathway in rat pulmonary arterial smooth muscle cells / P. Wang, X. Han , B. Mo [et al.] // Mol. Med. Rep. – 2017. – Vol. 16, №3. – P. 3111-3116. doi: 10.3892/mmr.2017.6983.

21. Maternal High-Fat Feeding Increases Placental Lipoprotein Lipase Activity by Reducing SIRT1 Expression in Mice / L. Qiao, Z. Guo, C. Bosco [et al.] // Diabetes. –2015. – Vol. 64, №9. – P. 3111-3120. doi: 10.2337/db14-1627.

22. Omega-3 fatty acids prevent hepatic steatosis, independent of PPAR-α activity, in a murine model of parenteral nutrition-associated liver disease / E. Prince, F.B. Lazare, W.R. Treem [et al.] // JPEN J. Parenter. Enteral. Nutr. – 2014. – Vol. 38, №5. – P. 608-616. doi: 10.1177/0148607113491436.

23. Palmitic Acid and β-Hydroxybutyrate Induce Inflammatory Responses in Bovine Endometrial Cells by Activating Oxidative Stress-Mediated NF-κB Signaling / P. Li , L. Li, C. Zhang [et al.] // Molecules. – 2019. – Vol. 24, №13. P. 2421. doi:10.3390/molecules24132421.

24. Palmitic Acid-Induced Podocyte Apoptosis via the Reactive Oxygen Species-Dependent Mitochondrial Pathway / T. Liu, X.M. Chen, J.Y. Sun [et al.] // Kidney Blood Press. Res. – 2018. – Vol. 43, №1. – P. 206-219. doi: 10.1159/000487673.

25. Peroxisome proliferator-activated receptor γ mediates porcine placental angiogenesis through hypoxia inducible factor-, vascular endothelial growth factor-and angiopoietin mediated signaling / J. Zhang, X. Peng, A. Yuan [et al.] // Mol. Med. Rep. – 2017.– Vol. 16, №3. – P. 2636-2644. doi:10.3892/mmr.2017.6903.

26. Placental DNA and mRNA levels of PPARγ and LXRα and their relationship to birth weight / A.P. Meher, N. Wadhwani, K. Randhir [et al.] // J. Clin. Lipidol. – 2016. – Vol. 10, №4. – P. 767-774. doi:10.1016/j.jacl.2016.02.004.

27. PPAR Action in Human Placental Development and Pregnancy and Its Complications / F. Wieser, L. Waite, C. Depoix [et al.] // PPAR Res. – 2008. – №2008. – P. 527048. doi:10.1155/2008/527048.

28. PPARγ controls pregnancy outcome through activation of EG-VEGF: new insights into the mechanism of placental development / V. Garnier, W. Traboulsi, A. Salomon [et al.] // Am. J. Physiol. Endocrinol. Metab. – 2015. – Vol. 309, №4. – e357-e369. doi:10.1152/ajpendo.00093.2015.

29. Protective role of GPR120 in the maintenance of pregnancy by promoting decidualization via regulation of glucose metabolism / J. Huang, M. Xue, J. Zhang [et al.] // EBioMedicine. – 2019. – № 39. – P. 540-551. doi:10.1016/j.ebiom.2018.12.019.

30. Rogero M.M. Obesity, Inflammation, TollLike Receptor 4 and Fatty Acids / M.M. Rogero // Nutrients. – 2018. –Vol. 10, №4. –P. 432. doi:10.3390/nu10040432.

31. Saturated fatty acids enhance TLR4 immune pathways in human trophoblasts / X. Yang, M. Haghiac, P. Glazebrook [et al.] // Hum. Reprod. – 2015. – Vol. 30, №9. – P. 2152-2159. doi:10.1093/humrep/dev173.

32. Saturated and unsaturated fatty acids differentially regulate in vitro and ex vivo placental antioxidant capacity / C.R. Manuel, M.J. Charron, C. Ashby [et al.] // Am. J. Reprod. Immunol. 2018. – Vol. 80, №3. – e12868. doi:10.1111/aji.12868.

33. Schistosome egg antigens elicit a proinflammatory response by trophoblast cells of the human placenta / E.A. McDonald, J.D. Kurtis, L. Acosta [et al.] // Infect. Immun. – 2013. – Vol. 81, №3. – P. 704-712. doi: 10.1128/IAI.01149-12.

34. Shimizu T. Lipid mediators in health and disease: enzymes and receptors as therapeutic targets for the regulation of immunity and inflammation / T. Shimizu //Annu. Rev. Pharmacol. Toxicol. – 2009. – № 49. – P.123-50. doi: 10.1146/annurev.pharmtox.011008.145616.

35. The peroxisome proliferator-activated receptors under epigenetic control in placental metabolism and fetal development / A. Lendvai, M.J. Deutsch, T. Plösch [et al.] // Am. J. Physiol. Endocrinol. Metab. – 2016. – Vol. 310, №10. – e797-e810. doi:10.1152/ajpendo.00372.2015.

36. Tube formation in the first trimester placental trophoblast cells: Differential effects of angiogenic growth factors and fatty acids / D. Pandya, M.K. Das, A. Sarkar [et al.] // Cell. Biol. Int. – 2016. – Vol. 40, №6. – P. 652-661. doi:10.1002/cbin.10601.


Review

For citations:


Ishutina N.A., Andrievskaya I.A., German M.N. Signaling functions of fatty acids in the placenta. Yakut Medical Journal. 2021;(1):92-97. https://doi.org/10.25789/YMJ.2021.73.25

Views: 17


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


ISSN 1813-1905 (Print)
ISSN 2312-1017 (Online)