外泌体源微小RNA与子痫前期发病机制研究新进展
Recent Advances in Exosomal MicroRNA and Pathogenesis of Pre-Eclampsia
DOI: 10.12677/ACM.2023.131128, PDF,    科研立项经费支持
作者: 李书明*:海南医学院,海南 海口;海南医学院第二附属医院产科,海南 海口;关红琼#:海南医学院第二附属医院产科,海南 海口
关键词: 子痫前期外泌体微小RNA滋养细胞炎症血管内皮细胞Pre-Eclampsia Exosomes MicroRNAs Trophoblasts Inflammatory Endothelial Cell
摘要: 子痫前期(Pre-Eclampsia, PE)是一种发生于妊娠20周后的妊娠特异性疾病,伴随着高血压、蛋白尿或其他脏器功能损害,属于妊娠期高血压疾病的一种。其发病率和死亡率较高,严重影响母婴健康。目前有关的发病机制学说有“两阶段学说、炎症免疫学说、遗传学说”等,但发病机制尚未完全阐明。通过阅读临床文献,发现外泌体以其自身独特的结构及功能优势受到学者们的青睐,研究有关他们的分泌、组成、功能及精确分子机制已蔚然成风。其中,对于PE发病机制与相关外泌体源微小RNA (microRNA, miRNA)的研究亦日益增多,因此本文对外泌体源miRNA与PE相关机制的研究进展进行综述。
Abstract: Pre-eclampsia (PE) is a pregnancy-specific disorder occurring after 20 weeks of gestation, accompa-nied by hypertension, proteinuria or other organ dysfunction. It is a kind of hypertensive disorder during pregnancy. It has high morbidity and mortality rates and seriously affects maternal and in-fant health. However, the pathogenesis has not been fully elucidated. At present, the pathogenesis theories of PE include “two-stage theory”, “inflammatory immune theory” and “genetic theory”. In recent years, exosomes have been favored by scholars for their unique structural and functional advantages, and the study of their secretion, composition, function and precise molecular mecha-nism has become a trend. Among them, studies on the pathogenesis of PE and related exo-some-derived microRNAs (miRNAs) are also increasing. Exosome-derived miRNAs regulate the function of target genes through the principle of base complementary matching and participate in various processes of the pathophysiology of PE. Therefore, this article reviews the research progress on the mechanisms related to exosome-derived miRNA and PE.
文章引用:李书明, 关红琼. 外泌体源微小RNA与子痫前期发病机制研究新进展[J]. 临床医学进展, 2023, 13(1): 887-893. https://doi.org/10.12677/ACM.2023.131128

参考文献

[1] Lip, S.V., Boekschoten, M.V., Hooiveld, G.J., et al. (2020) Early-Onset Preeclampsia, Plasma microRNAs, and Endo-thelial Cell Function. American Journal of Obstetrics & Gynecology, 222, 497.e1-497.e12. [Google Scholar] [CrossRef] [PubMed]
[2] Li, H., Ouyang, Y., Sadovsky, E., et al. (2020) Unique mi-croRNA Signals in Plasma Exosomes from Pregnancies Complicated by Preeclampsia. Hypertension, 75, 762-771. [Google Scholar] [CrossRef
[3] Biró, O., Fóthi, Á., Alasztics, B., et al. (2019) Circulating Exosomal and Argonaute-Bound microRNAs in Preeclampsia. Gene, 692, 138-144. [Google Scholar] [CrossRef] [PubMed]
[4] Mincheva-Nilsson, L. and Baranov, V. (2014) Placenta-Derived Exosomes and Syncytiotrophoblast Microparticles and Their Role in Human Reproduction: Immune Modulation for Pregnancy Success. American Journal of Reproductive Immunology, 72, 440-457. [Google Scholar] [CrossRef] [PubMed]
[5] Salomon, C., Torres, M.J., Kobayashi, M., et al. (2014) A Gestational Pro-file of Placental Exosomes in Maternal Plasma and Their Effects on Endothelial Cell Migration. PLOS ONE, 9, e98667. [Google Scholar] [CrossRef] [PubMed]
[6] Wang, Z., Wang, P., Wang, Z., et al. (2019) MiRNA-548c-5p Downregulates Inflammatory Response in Preeclampsia via Targeting PTPRO. Journal of Cellular Physiology, 234, 11149-11155. [Google Scholar] [CrossRef] [PubMed]
[7] Salomon, C., Guanzon, D., Scholz-Romero, K., et al. (2017) Placental Exosomes as Early Biomarker of Preeclampsia: Potential Role of Exosomal MicroRNAs across Gestation. The Journal of Clinical Endocrinology & Metabolism, 102, 3182-3194. [Google Scholar] [CrossRef] [PubMed]
[8] Qu, H. and Khalil, R.A. (2020) Vascular Mechanisms and Molecular Targets in Hypertensive Pregnancy and Preeclampsia. American Journal of Physiology-Heart and Circulatory Physiology, 319, H661-H681. [Google Scholar] [CrossRef] [PubMed]
[9] Ntie, E., Kere, J., Kivinen, K., et al. (2017) Analysis of Comple-ment C3 Gene Reveals Susceptibility to Severe Preeclampsia. Frontiers in Immunology, 8, Article No. 589. [Google Scholar] [CrossRef] [PubMed]
[10] Levine, L., Habertheuer, A., Ram, C., et al. (2020) Syncytiotrophoblast Extracellular Microvesicle Profiles in Maternal Circulation for Noninvasive Diagnosis of Preeclampsia. Scientific Reports, 10, Article No. 6398. [Google Scholar] [CrossRef] [PubMed]
[11] Harding, C.V., Heuser, J.E. and Stahl, P.D. (2013) Exosomes: Looking Back Three Decades and into the Future. Journal of Cell Biology, 200, 367-371. [Google Scholar] [CrossRef] [PubMed]
[12] Lycoudi, A., Mavreli, D., Mavrou, A., et al. (2015) miRNAs in Preg-nancy-Related Complications. Expert Review of Molecular Diagnostics, 15, 999-1010. [Google Scholar] [CrossRef] [PubMed]
[13] Bounds, K.R., Chiasson, V.L., Pan, L.J., et al. (2017) Mi-croRNAs: New Players in the Pathobiology of Preeclampsia. Frontiers in Cardiovascular Medicine, 4, 60. [Google Scholar] [CrossRef] [PubMed]
[14] Ge, Q., Zhou, Y., Lu, J., et al. (2014) miRNA in Plasma Exosome Is Stable under Different Storage Conditions. Molecules, 19, 1568-1575. [Google Scholar] [CrossRef] [PubMed]
[15] Awamleh, Z., Gloor, G.B. and Han, V.K.M. (2019) Placental mi-croRNAs in Pregnancies with Early Onset Intrauterine Growth Restriction and Preeclampsia: Potential Impact on Gene Expression and Pathophysiology. BMC Medical Genomics, 12, 91. [Google Scholar] [CrossRef] [PubMed]
[16] Morales-Prieto, D.M., Ospina-Prieto, S., Chaiwangyen, W., et al. (2013) Pregnancy-Associated miRNA-Clusters. Journal of Reproductive Immunology, 97, 51-61. [Google Scholar] [CrossRef] [PubMed]
[17] Hromadnikova, I., Dvorakova, L., Kotlabova, K., et al. (2019) The Prediction of Gestational Hypertension, Preeclampsia and Fetal Growth Restriction via the First Trimester Screening of Plasma Exosomal C19MC microRNAs. International Journal of Molecular Sciences, 20, 2972. [Google Scholar] [CrossRef] [PubMed]
[18] Huang, Q., Gong, M., Tan, T., et al. (2021) Human Umbilical Cord Mesenchymal Stem Cells-Derived Exosomal MicroRNA-18b-3p Inhibits the Occurrence of Preeclampsia by Targeting LEP. Nanoscale Research Letters, 16, 27. [Google Scholar] [CrossRef] [PubMed]
[19] Pillay, P., Vatish, M., Duarte, R., et al. (2019) Exosomal mi-croRNA Profiling in Early and Late Onset Preeclamptic Pregnant Women Reflects Pathophysiology. International Jour-nal of Nanomedicine, 14, 5637-5657. [Google Scholar] [CrossRef
[20] Motawi, T.M.K., Sabry, D., Maurice, N.W., et al. (2018) Role of Mes-enchymal Stem Cells Exosomes Derived microRNAs, miR-136, miR-494 and miR-495 in Pre-Eclampsia Diagnosis and Evaluation. Archives of Biochemistry and Biophysics, 659, 13-21. [Google Scholar] [CrossRef] [PubMed]
[21] Ji, L., Brkić, J., Liu, M., et al. (2013) Placental Trophoblast Cell Differentiation: Physiological Regulation and Pathological Relevance to Preeclampsia. Molecular Aspects of Medicine, 34, 981-1023. [Google Scholar] [CrossRef] [PubMed]
[22] Lu, J., Sun, Y., Cao, Y., et al. (2022) Small RNA Sequencing Re-veals Placenta-Derived Exosomal microRNAs Associated with Preeclampsia. Journal of Hypertension, 40, 1030-1041. [Google Scholar] [CrossRef
[23] Wang, D., Na, Q., Song, G.Y. and Wang, L.L. (2020) Hu-man Umbilical Cord Mesenchymal Stem Cell-Derived Exosome-Mediated Transfer of microRNA-133b Boosts Tropho-blast Cell Proliferation, Migration and Invasion in Preeclampsia by Restricting SGK1. Cell Cycle, 19, 1869-1883. [Google Scholar] [CrossRef] [PubMed]
[24] Kerbel, R.S. (2000) Tumor Angiogenesis: Past, Present and the Near Future. Carcinogenesis, 21, 505-515. [Google Scholar] [CrossRef] [PubMed]
[25] Fagiani, E. and Christofori, G. (2013) Angiopoietins in Angiogenesis. Cancer Letters, 328, 18-26. [Google Scholar] [CrossRef] [PubMed]
[26] Zhao, X.Y., et al. (2020) Exosomal Encapsulation of miR-125a-5p Inhibited Trophoblast Cell Migration and Proliferation by Regulating the Expression of VEGFA in Preeclampsia. Biochemical and Biophysical Research Communications, 525, 646-653. [Google Scholar] [CrossRef] [PubMed]
[27] Shen, L., Li, Y., Li, R., et al. (2018) Placenta-Associated Serum Exosomal miR-155 Derived from Patients with Preeclampsia Inhibits eNOS Expression in Human Umbilical Vein En-dothelial Cells. International Journal of Molecular Medicine, 41, 1731-1739. [Google Scholar] [CrossRef] [PubMed]
[28] Pugh, C.W. and Ratcliffe, P.J. (2003) Regulation of Angiogenesis by Hypoxia: Role of the HIF System. Nature Medicine, 9, 677-684. [Google Scholar] [CrossRef] [PubMed]
[29] Liang, H., Xiao, J., Zhou, Z., et al. (2018) Hypoxia Induces miR-153 through the IRE1α-XBP1 Pathway to Fine Tune the HIF1α/VEGFA Axis in Breast Cancer Angiogenesis. Oncogene, 37, 1961-1975. [Google Scholar] [CrossRef] [PubMed]
[30] Liang, H., Ge, F., Xu, Y., et al. (2018) miR-153 Inhibits the Mi-gration and the Tube Formation of Endothelial Cells by Blocking the Paracrine of Angiopoietin 1 in Breast Cancer Cells. Angiogenesis, 21, 849-860. [Google Scholar] [CrossRef] [PubMed]
[31] Ma, H.Y., Cu, W., Sun, Y.H., et al. (2020) MiRNA-203a-3p In-hibits Inflammatory Response in Preeclampsia through Regulating IL24. European Review for Medical and Pharmaco-logical Sciences, 24, 5223-5230.
[32] Taga, S., Hayashi, M., Nunode, M., et al. (2022) miR-486-5p Inhibits Invasion and Migration of HTR8/SVneo Trophoblast Cells by Down-Regulating ARHGAP5. Placenta, 123, 5-11. [Google Scholar] [CrossRef] [PubMed]
[33] Ma, R., Liang, Z., Shi, X., et al. (2021) Exosomal miR-486-5p Derived from Human Placental Microvascular Endothelial Cells Regulates Proliferation and Invasion of Trophoblasts via Targeting IGF1. Human Cell, 34, 1310-1323. [Google Scholar] [CrossRef] [PubMed]
[34] 许洪梅, 张媛, 章乐霞, 等. lnc-SNHG5及miR-155在子痫前期患者血清及外泌体中的表达及其胎盘源性检测[J]. 中国计划生育和妇产科, 2022, 14(2): 85-88+104.