ИММУНОЛОГИЧЕСКИЕ МЕХАНИЗМЫ КОНТРОЛЯ АПОПТОЗА ПРИ РАЗВИТИИ ПЛАЦЕНТЫ
https://doi.org/10.15789/1563-0625-2008-2-3-125-138
Аннотация
Резюме. В настоящем обзоре рассмотрены известные на сегодня сведения о роли иммунологических механизмов контроля процессов апоптоза на разных этапах развития плаценты. Интенсивность процессов апоптоза в человеческой плаценте прогрессивно увеличивается на протяжении всей беременности вплоть до родоразрешения. Индукция и предотвращение апоптоза в клетках плаценты – процессы, неразрывно связанные с развитием плаценты и формированием сосудистого дерева, контролируемые клетками трофобласта, а также клетками иммунной системы матери и плода. Т-лимфоциты, NK-клетки, NKT-клетки и макрофаги осуществляют надзор за процессами ангиогенеза и апоптоза в ткани плаценты, обеспечивая ее нормальное развитие и функционирование. Работа поддержана грантами Президента РФ № НШ-5268.2006.7 и МК-1355.2007.7.
Об авторе
Д. И. СоколовРоссия
Лаборатория иммунологии
199282, Санкт-Петербург, ул. Крыленко, 45, корп. 1, кв. 5
Список литературы
1. Павлов О.В., Сельков С.А., Селютин С.А., Ананьева В.В. Секреция фактора некроза опухоли-α и интерлейкина-1 плацентарными макрофагами in vitro при различных исходах беременности // Бюлл. экспер. биол. и мед. – 1999. – № 7. – С. 97-100.
2. Соколов Д.И., Селютин А.В., Лесничия М.В., Аржанова О.Н., Сельков С.А. Cубпопуляционный состав лимфоцитов периферической крови беременных женщин с гестозом // Журнал акушерства и женских болезней. – 2007. – № 4, Том LVIII. – С.15-18.
3. Ширшев С.В. Механизмы иммунного контроля процессов репродукции.— Екатеринбург, 1999. – 383 с.
4. Фрейдлин И.C., Тотолян А.А. Клетки иммунной системы – СПб.: Наука, 2001. – Т. 3. – 456 с.
5. Ярилин А.А. Апоптоз: природа феномена и его роль в норме и при патологии // Актуальные проблемы патофизиологии / Под ред. Б.Б. Мороза. – М.: Медицина, 2001. – С. 13-56.
6. Abrahams V.M., Kim Y.M., Straszewski S.L., Romero R., Mor G. Macrophages and apoptotic cell clearance during pregnancy // Am. J. Reprod. Immunol. – 2004. – Vol. 51. – P. 275-282.
7. Abrahams V.M., Straszewski-Chavez S.L., Guller S., Mor G. First trimester trophoblast cells secrete Fas ligand which induces immune cell apoptosis // Mol. Hum. Reprod. – 2004. – Vol. 10. – P. 55-63.
8. Aggarwal B.B. Signalling pathways of the TNF superfamily: double-edged sword // Nat. Rev. Immunol. – 2003. – Vol. 3. – P. 745-756.
9. Allaire A.D., Ballenger K.A., Wells S.R., McMahon M.J., Lessey B.A. Placental apoptosis in preeclampsia // Obstet. Gynecol. – 2000. – Vol. 96. – P. 271-276.
10. Alon T., Hemo I., Itin A., Peer J., Stone J., Keshet E. Vascular endothelial growth factor acts as a survival factor for newly formed retinal vessels and has implications for retinopathy of prematurity // Nature Med. – 1995. – Vol. 1. – P. 1024-1028.
11. Asahara T., Masuda H., Takahashi T., Kalka C., Pastore C., Silver M., Kearne M., Magner M., Isner J.M. Bone marrow origin of endothelial progenitor cells responsible for postnatal vasculogenesis in physiological and pathological neovascularization // Circ. Res. – 1999. – Vol. 85. – P. 221-228.
12. Aschkenazi S., Straszewski S., Verwer K.M., Foellmer H., Rutherford T., Mor G. Differential regulation and function of the fas/fas ligand system in human trophoblast cells // Biol. Reprod. 2002. – Vol. 66. – P. 1853-1861.
13. Ashton S.V., Whitley G.S., Dash P.R., Wareing M., Crocker I.P., Baker P.N., Cartwright J.E. Uterine spiral artery remodeling involves endothelial apoptosis induced by extravillous trophoblasts through Fas/FasL interactions // Arterioscler. Thromb. Vasc. Biol. – 2005. – Vol. 25. – P. 102-108.
14. Bachmayer N., Rafik Hamad R., Liszka L., Bremme K. Aberrant uterine natural killer (NK)-cell expression and altered placental and serum levels of the NK-cell promoting cytokine interleukin-12 in pre-eclampsia // Am. J. Reprod. Immunol. – 2006. – Vol. 56, N 5-6. – P. 292-301.
15. Bennett W.A., Lagoo-Deenadayalan S., Stopple J.A., Barber W.H., Hale E., Brackin M.N., Cowan B.D. Cytokine expression by first-trimester human chorionic villi // Am. J. Reprod. Immunol. – 1998. – Vol. 40. – P. 309-318.
16. Borzychowski A.M., Croy B.A., Chan W.L., Redman C.W. Changes in systemic type 1 and type 2 immunity in normal pregnancy and pre-eclampsia may be mediated by natural killer cells // Eur. J. Immunol. – 2005. – Vol. 35, N 10. – P. 3054-3063.
17. Breitschopf K., Haendeler J., Malchow P., Zeiher A.M., Dimmeler S. Posttranscriptional modification of Bcl-2: molecular characterization of the involved signaling pathways // Mol. Cell. Biol. – 2000. – Vol. 20. – P. 1886-1896.
18. Brown S.B., Savill J. Phagocytosis triggers macrophage release of Fas ligand and induces apoptosis of bystander leukocytes // J. Immunol. – 1999. – Vol. 162. – P. 480-485.
19. Cai J., Ahmad S., Jiang W.G., Huang J., Kontos C.D., Boulton M., Ahmed A. Activation of vascular endothelial growth factor receptor-1 sustains angiogenesis and bcl-2 expression via the phosphatidylinositol 3-kinase pathway in endothelial cells // Diabetes. – 2003. – Vol. 52, N 12. – P. 2959-2968.
20. Calucci L., Pinzino C., Zandomeneghi M., Capocchi A., Ghiringhelli S., Saviozzi F., Tozzi S., Galleschi L. Effects of gamma-irradiation on the free radical and antioxidant contents in nine aromatic herbs and spices // J. Agric. Food. Chem. – 2003. – Vol. 12, N 4. – P. 927-34.
21. Carmeliet P., Ferreira V., Breier G., Pollefeyt S., Kieckens L., Gertsenstein M., Fahrig M., Vandenhoeck A., Harpal K., Eberhardt C., Declercq C., Pawling J., Moons L., Collen D., Risau W., Nagy A. Abnormal blood vessel development and lethality in embryos lacking a single VEGF allele // Nature. – 1996. – Vol. 380. – P. 435- 439.
22. Carmeliet P., Lampugnani M.G., Moons L., Breviario F., Compernolle V., Bono F., Balconi G., Spagnuolo R., Oostuyse B., Dewerchin M., Zanetti A., Angellilo A., Mattot V., Nuyens D., Lutgens E., Clotman F., de Ruiter M.C., Gittenberger-de Groot A., Poelmann R., Lupu F., Herbert J.M., Collen D., Dejana E. Targeted deficiency or cytosolic truncation of the VE-cadherin gene in mice impairs VEGF-mediated endothelial survival and angiogenesis // Cell. – 1999. – Vol. 98. – P. 147-157.
23. Casey M.L., Cox S.M., Word R.A., MacDonald P.C. Cytokines and infection-induced preterm labour // Reprod. Fertil. Dev. – 1990. – Vol. 2. – P. 499-509.
24. Castellucci M., Kaufmann P. Hofbauer cells // Pathology of the Human Placenta / Ed. by K. Benirschke, P. Kaufmann. – 2nd ed. – New York: Springer, 1992. – P. 71-80.
25. Cavaillon J.M. Cytokines and macrophages // Biomed. Pharmacother. – 1994. – Vol. 48. – P. 445-453.
26. Challis J.R.G., Matthews S.G., Gibb W., Lye S.J. Endocrine and paracrine regulation of birth at term and preterm // Endocrine Reviews. – 2000. – Vol. 21, N 5. – P. 514-550.
27. Chaouat G., Ledee-Bataille N., Dubanchet S., Zourbas S., Sandra O., Martal J. TH1/TH2 paradigm in pregnancy: paradigm lost? Cytokines in pregnancy/early abortion: reexamining the TH1/TH2 paradigm // Int. Arch. Allergy Immunol. – 2004. – Vol. 134. – P. 93-119.
28. Charnock-Jones D.S., Kaufmann P., Mayhew T.M. Aspects of human fetoplacental vasculogenesis and angiogenesis. I. Molecular regulation // Placenta. – 2004. – Vol. 25. – P. 103-113.
29. Cheng J., Zhou T., Liu C., Shapiro J.P., Bra - uer M.J., Kiefer M.C., Barr P.J., Mountz J.D. Protection from Fas-mediated apoptosis by soluble form of the Fas molecule // Science. – 1994. – Vol. 263. – P. 1759-1762.
30. Cirelli N., Moens A., Lebrun P., Gueuning C., Delogne-Desnoeck J., Vanbellinghen A.-M., Meu ris S. Apoptosis in human term placenta is not increased during labor but can be massively induced in vitro // Biol. of Reproduction. – 1999. – Vol. 61. – P. 458-463.
31. Clark D.E., Charnock-Jones D.S. Placental angiogenesis: role of the VEGF family of proteins // Angiogenesis. – 1998. – Vol. 2, N 4. – P. 309-318.
32. Clark D.E., Smith S.K., He Y., Day K.A., Licence D.R., Corps A.N., Lammoglia R., Charnock-Jones D.S. A vascular endothelial growth factor antagonist is produced by the human placenta and released into the maternal circulation // Biol. of Reprod. – 1998. – Vol. 59. – P. 1540-1548.
33. Crocker I.P., Cooper S., Ong S.C., Baker P.N. Differences in apoptotic susceptibility of cytotrophoblasts and syncytiotrophoblasts in normal pregnancy to those complicated with preeclampsia and intrauterine growth restriction // Am. Pathol. – 2003. – Vol. 162. – P. 637-643.
34. Dhanabal M., Ramchandran R., Waterman M.J., Lu H., Knebelmann B., Segal M., Sukhatme V.P. Endostatin induces endothelial cell apoptosis // J. Biol. Chem. – 1999. – Vol. 274. – P. 11721-11726.
35. Desai J., Holt-Shore V., Torry R.J., Caud- le M.R., Torry D.S. Signal transduction and biological function of placenta growth factor in primary human trophoblast // Biol. Reprod. – 1999. – Vol. 60. – P. 887-892.
36. Dimmeler S., Breitschopf K., Haendeler J., Zeiher A.M. Dephosphorylation targets Bcl-2 for ubiquitin-dependent degradation: a link between the apoptosome and the proteasome pathway // J. Exp. Med. – 1999. – Vol. 189. – P. 1815-1822.
37. Dimmeler S., Zeiher A.M. Endothelial cell apoptosis in angiogenesis and vessel regression // Circ. Res. – 2000. – Vol. 87. – P. 434-439.
38. Duffield J.S., Ware C.F., Ryffel B., Savill J. Suppression by apoptotic cells defines tumor necrosis factor-mediated induction of glomerular mesangial cell apoptosis by activated macrophages // Am. J. Pathol. – 2001. – Vol. 159. – P. 1397-1404.
39. Dunk C., Petkovic L., Baczyk D., Rossant J., Winterhager E., Lye S. A novel in vitro model of trophoblast-mediated decidual blood vessel remodeling // Lab. Invest. – 2003. – Vol. 83. – P. 1821-1828.
40. Enari M., Sakahira H., Yokoyama H., Okawa K., Iwamatsu A., Nagata S. A caspase-activated DNase that degrades DNA during apoptosis, and its inhibitor ICAD // Nature. – 1998. – Vol. 391. – P. 43-50.
41. Ehrhardt H., Fulda S., Schmid I., Hiscott J., Debatin K.M., Jeremias I. TRAIL induced survival and proliferation in cancer cells resistant towards TRAIL-induced apoptosis mediated by NF-κB // Oncogene. – 2003. – Vol. 22. – P. 3842-3852.
42. Ferrara N. Role of vascular endothelial growth factor in regulation of physiological angiogenesis // Am. J. Physiol. Cell Physiol. – 2001. – Vol. 280. – P. 1358-1366.
43. Fischer U., Janicke R.U., Schulze-Osthoff K. Many cuts to ruin: comprehensive update of caspase substrates // Cell Death Differ. – 2003. – Vol. 10. – P. 76-100.
44. Formby B. Immunologic response in pregnancy. Its role in endocrine disorders of pregnancy and influence on the course of maternal autoimmune diseases // Endocrinol. Metab. Clin. North Am. – 1995. – Vol. 24. – P. 187-205.
45. Galan A., O’Connor J.E., Valbuena D., Herrer R., Remohi J., Pampfer S., Pellicer A., Simon C. The human blastocyst regulates endometrial epithelial apoptosis in embryonic adhesion // Biol. Reprod. – 2000. – Vol. 63. – P. 430-439.
46. Gerber H.P., Dixit V., Ferrara N. Vascular endothelial growth factor induces expression of the antiapoptotic proteins Bcl-2 and A1 in vascular endothelial cells // J. Biol. Chem. – 1998. – Vol. 273. – P. 13313-13316.
47. Geva E., Ginzinger D.G., Zaloudek C.J., Moore D.H., Byrne A., Jaffe R.B. Human placental vascular development: vasculogenic and angiogenic (branching and nonbranching) transformation is regulated by vascular endothelial. Growth factor-a, angiopoietin-1, and angiopoietin-2 // J. Clin. Endocrin. Metab. – 2002. – Vol. 87, N 9. – P. 4213-4224.
48. Hammer A., Blaschitz A., Daxbock C., Walcher W., Dohr G. Fas and Fas-ligand are expressed in the uteroplacental unit of firsttrimester pregnancy // Am. J. Reprod. Immunol. – 1999. – Vol. 41. – P. 41-51.
49. Hirata H., Takahashi A., Kobayashi S., Yonehara S., Sawai H., Okazaki T., Yamamoto K. Caspases are activated in branched protease cascade and control distinct downstream processes in Fasinduced apoptosis // Exp. Med. – 1998. – Vol. 187. – P. 587-600.
50. Hung T.-H., Skepper J.N., Charnock-Jones D.S., Burton G.J. Hypoxia-reoxygenationa potent inducer of apoptotic changes in the human placenta and possible etiological factor in preeclampsia // Circ. Res. – 2002. – Vol. 90. – P. 1274-1281.
51. Hunt J.S. Cytokine networks in the uteroplacental unit: Macrophages as pivotal regulatory cells // J. Reprod. Immunol. – 1989. – Vol. 16. – P. 1-17.
52. Huppertz B., Tews D.S., Kaufmann P. Apoptosis and syncytial fusion in human placental trophoblast and skeletal muscle // Int. Rev. Cytol. – 2001. – Vol. 205. – P. 215-253.
53. Huppertz B., Frank H.G., Kingdom J.C., Reister F., Kaufmann P. Villous cytotrophoblast regulation of the syncytial apoptotic cascade in the human placenta // Histochem. Cell Biol. – 1998. – Vol. 110. – P. 495-508.
54. Huppertz B., Kingdom J.C. Apoptosis in the trophoblast – role of apoptosis in placental morphogenesis // J. Soc. Gynecol. Investig. – 2004. – Vol. 11. – P. 353-362.
55. Ishihara N., Matsuo H., Murakoshi H., Laoag-Fernandez J.B., Samoto T., Maruo T. Increased apoptosis in the syncytiotrophoblast in human term placentas complicated by either preeclampsia or intrauterinegrowth retardation // Am. J. Obstet. Gynecol. – 2002. – Vol. 186. – P. 158-166.
56. Itoh N., Nagata S. A novel protein domain required for apoptosis. Mutational analysis of human Fas antigen // Biol. Chem. – 1993. – Vol. 268. – P. 10932-10937.
57. Jiang S.P., Vacchio M.S. Multiple mechanisms of peripheral T cell tolerance to the fetal allograft // J. Immunol. – 1998. – Vol. 160. – P. 3086-3090.
58. Jimenez B., Volpert O.V., Crawford S.E., Febbraio M., Silverstein R.L., Bouck N. Signals leading to apoptosis-dependent inhibition of neovascularization by thrombospondin-1 // Nat. Med. – 2000. – Vol. 6. – P. 41-48.
59. Kalka C., Masuda H., Takahashi T., Gordon R., Tepper O., Gravereaux E., Pieczek A., Iwaguro H., Hayashi S.I., Isner J.M., Asahara T. Vascular endothelial growth factor(165) gene transfer augments circulating endothelial progenitor cells in human subjects // Circ. Res. – 2000. – Vol. 86. – P. 1198-1202.
60. Kaufmann P., Black S., Huppertz B. Endovascular trophoblast invasion: implications for the pathogenesis of intrauterine growth retardation and preeclampsia // Biol. Reprod. – 2003. – Vol. 69. – P. 1-7.
61. Kaufmann P., Mayhew T.M. Charnock-Jones D.S. Aspects of human fetoplacental vasculogenesis and angiogenesis. II. Molecular regulation // Placenta. – 2004. – Vol. 25. – P. 114-126.
62. Kauma S.W., Huff T.F., Hayes N., Nilkaeo A. Placental Fas ligand expression is a mechanism for maternal immune tolerance to the fetus // J. Clin. Endocrinol. Metab. – 1999. – Vol. 84. – P. 2188-2194.
63. Kerr J.F.R., Wyllie A.H., Currie A.R. Apoptosis, a basic biological phenomenon with wide-ranging implications in tissue kinetics // Br. J. Cancer. – 1972. – Vol. 26. – P. 239-257.
64. Khong T.Y. Immunohistologic study of the leukocytic infiltrate in maternal uterine tissues in normal and preeclamptic pregnancies at term // Am. J. Reprod. Immunol. Microbiol. – 1987. – Vol. 15. – P. 1-8.
65. Kim C.J., Choe Y.J., Yoon B.H., Kim C.W., Chi J.G. Patterns of bcl-2 expression in placenta // Pathol. Res. Pract. – 1995. – Vol. 191. – P. 1239-1244.
66. Kim I., Kim H.G., So J.-N., Kim J.H., Kwak H.J., Koh G.Y. Angiopoietin-1 regulates endothelial cell survival through the phosphatidylinositol 39-kinase/Akt signal transduction pathway // Circ. Res. – 2000. – Vol. 86. – P. 24-29.
67. Knofler M., Mosl B., Bauer S., Griesinger G., Husslein P. TNF-α/TNFRI in primary and immortalized first trimester cytotrophoblasts // Placenta. – 2000. – Vol. 21. – P. 525-535.
68. Koh E.A., Illingworth P.J., Duncan W.C., Critchley H.O. Immunolocalization of bcl-2 protein in human endometrium in the menstrual cycle and stimulated early pregnancy // Hum. Reprod. – 1995. – Vol. 10. – P. 1557-1562.
69. Kudo T., Izutsu T., Sato T. Telomerase activity and apoptosis as indicators of ageing in placenta with and without intrauterine growth retardation // Placenta. – 2000. – Vol. 21. – P. 493-500.
70. Lucas R., Holmgren L., Garcia I., Jimenez B., Mandriota S.J., Borlat F., Sim B.K., Wu Z., Grau G.E., Shing Y., Soff G.A., Bouck N., Pepper M.S. Multiple forms of angiostatin induce apoptosis in endothelial cells // Blood. – 1998. – Vol. 92. – P. 4730-4741.
71. Mayhew T.M., Leach L., McGee R., Ismail W.W., Myklebust R., Lammiman M.J. Proliferation, differentiation and apoptosis in villous trophoblast at 13-41 weeks of gestation (including observations on annulate lamellae and nuclear pore complexes) // Placenta. – 1999. – Vol. 20. – P. 407-422.
72. Mayhew T.M. Villous trophoblast of human placenta: coherent view of its turnover, repair and contributions to villous development and maturation // Histol. Histopathol. – 2001. – Vol. 16. – P. 1213-1224.
73. Menier C., Riteau B., Carosella E.D., Rouas-Freiss N. MICA triggering signal for NK cell tumor lysis is counteracted by HLA-G1-mediated inhibitory signal // Int. J. Cancer. – 2002. – Vol. 100. – P. 63-70.
74. Miyashita T., Reed J.C. Tumor suppressor p53 is direct transcriptional activator of the human bax gene // Cell. – 1995. – Vol. 80. – P. 293-299.
75. Mor G., Abrahams V.M. Potential role of macrophages as immunoregulators of pregnancy // Reprod. Biol. Endocrinol. – 2003. – Vol. 1. – P. 119-126.
76. Mor G., Gutierrez L.S., Eliza M., Kahyaoglu F., Arici A. Fas-fas ligand system-induced apoptosis in human placenta and gestational trophoblastic disease // Am. J. Reprod. Immunol. – 1998. – Vol. 40. – P. 89-94.
77. Moreau P., Adrian-Cabestre F., Menier C., Guiard V., Gourand L., Dausset J., Carosella E.D., Paul P. IL-10 selectively induces HLA-G expression in human trophoblasts and monocytes // Int. Immunol. – 1999. – Vol. 11. – P. 803-811.
78. Nor J.E., Polverini P.J. Role of endothelial cell survival and death signals in angiogenesis // Angiogenesis. – 1999. – Vol. 3. – P. 101-116.
79. Pijnenborg R., McLaughlin P.J., Vercruysse L., Hanssens M., Johnson P.M., Keith J.C. Immunolocalization of tumour necrosis factor-alpha (TNF-alpha) in the placental bed of normotensive and hypertensive human pregnancies // Placenta. – 1998. – Vol. 19. – P. 231-239.
80. Pimentel-Muinos F.X., Seed B. Regulated commitment of TNF receptor signaling: a molecular switch for death or activation // Immunity. – 1999. – Vol. 11. – P. 783-793.
81. Ratts V.S., Tao X.J., Webster C.B., Swanson P.F., Brownbill P., Sibley C., Reed J.C., Tilly J.L., Nel son D.M. Regulation of apoptotic cell death within the trophoblast layer: role of Bcl-2, Bax and Bak in the term human placenta // J. Soc. Gynecol. Invest. – 1998. – Vol. 5. – P. 126A.
82. Reister F., Frank H.G., Heyl W., Kosanke G., Huppertz B., Schröder W., Kaufmann P., Rath W. The distribution of macrophages in spiral arteries of the placental bed in pre-eclampsia differs from that in healthy patients // Placenta. – 1999. – Vol. 20. – P. 229-233.
83. Riley S.C., Webb C.J., Leask R., McCaig F.M., Howe D.C. Involvement of matrix metalloproteinases 2 and 9, tissue inhibitor of metalloproteinases and apoptosis in tissue remodelling in the sheep placenta // J. Reprod. Fertil. – 2000. – Vol. 118. – P. 19-27.
84. Riteau B., Menier C., Khalil-Daher I., Martinozzi S., Pla M., Dausset J., Carosella E.D., Rouas-Freiss N. HLA-G1 co-expression boosts the HLA class I-mediated NK lysis inhibition // Int. Immunol. – 2001. – Vol. 13. – P. 193-201.
85. Rodger F.E., Fraser H.M., Duncan W.C., Illingworth P.J. Immunolocalisation of bcl-2 in the human corpus luteum // Hum. Reprod. – 1995. – Vol. 10. – P. 1566-1570.
86. Rupp P.A., Little C.D. Integrins in Vascular Development // Circ. Res. – 2001. – Vol. 89. – P. 566-572.
87. Sabourin J.C., Martin A., Baruch J., Truc J.B., Gompel A., Poitout P. Bcl-2 expression in normal breast tissue during the menstrual cycle // Int. J. Cancer. – 1994. – Vol. 59. – P. 1-6.
88. Schuler M., Green D.R. Mechanisms of p53-dependent apoptosis // Biochem. Soc. Trans. – 2001. – Vol. 29. – P. 684-688.
89. Sargent I.L., Borzychowski A.M., Redman C.W. Immunoregulation in normal pregnancy and preeclampsia: an overview // Reprod. Biomed. Online. – 2006. – Vol. 13, N 5. – P. 680-686.
90. Sargent I.L., Borzychowski A.M., Redman C.W. NK cells and human pregnancy – an inflammatory view // Trends. Immunol. – 2006. – Vol. 27, N 9. – P. 399-404.
91. Siegel R.M., Frederiksen J.K., Zacharias D.A., Chan F.K., Johnson M., Lynch D., Tsien R.Y., Lenardo M.J. Fas preassociation required for apoptosis signaling and dominant inhibition by pathogenic mutations // Science. – 2000. – Vol. 288. – P. 2354-2357.
92. Smith S.C., Baker P.N., Symonds E.M. Placental apoptosis in normal human pregnancy // Am. J. Obstet. Gynecol. – 1997. – Vol. 177. – P. 57-65.
93. Smith S., Francis R., Guilbert L., Baker P.N. Growth factor rescue of cytokine mediated trophoblast apoptosis // Placenta. – 2002. – Vol. 23. – P. 322-330.
94. Sprick M.R., Walczak H. The interplay between the Bcl-2 family and death receptor-mediated apoptosis // Biochim. Biophys. Acta. – 2004. – Vol. 1644. – P. 125-132.
95. Straszewski-Chavez S.L., Abrahams V.M., Mor G. TNF-α induces trophoblast apoptosis by upregulating XIAP-associated factor 1 (XAF1) // J. Soc. Gynecol. Invest. – 2004. – Vol. 11. – P. 179A.
96. Suri C., Jones P.F., Patan S., Bartunkova S., Maisonpierre P.C., Davis S., Sato T.N., Yancopoulos G.D. Requisite role of angiopoietin-1, a ligand for the TIE2 receptor, during embryonic angiogenesis // Cell. – 1996. – Vol. 87. – P. 1171-1180.
97. Tachi C., Tachi S. Macrophages and implantation // Ann. NY Acad. Sci. – 1986. – Vol. 476. – P. 158-182.
98. Tafuri A., Alferink J., Moller P., Hammerling G.J., Arnold B. T cell awareness of paternal alloantigens during pregnancy // Science. – 1995. – Vol. 270. – P. 630-633.
99. Tapanainen J.S., Tilly J.L., Vihko K.K., Hsueh A.J. Hormonal control of apoptotic cell death in the testis, gonadotropins and androgens as testicular cell survival factors // Mol. Endocrinol. – 1993. – Vol. 7. – P. 643-650.
100. Uckan D., Steele A., Cherry A., Wang B.Y., Chamizo W., Koutsonikolis A., Gilbert-Barness E., Good R.A. Trophoblasts express Fas ligand: proposed mechanism for immune privilege in placenta and maternal invasion // Mol. Hum. Reprod. – 1997. – Vol. 3. – P. 655-662.
101. Voll R.E., Herrmann M., Roth E.A., Stach C., Kalden J.R., Girkontaite I. Immunosuppressive effects of apoptotic cells // Nature. – 1997. – Vol. 390. – P. 350-351.
102. Visser N., van Rijn B.B., Rijkers G.T., Franx A., Bruinse H.W. Inflammatory changes in preeclampsia: current understanding of the maternal innate and adaptive immune response // Obstet. Gynecol Surv. – 2007. – Vol. 62, N 3. – P. 191-201.
103. Wang J., Chun H.J., Wong W., Spencer D.M., Lenardo M.J. Caspase-10 is an initiator caspase in death receptor signaling // Proc. Natl. Acad. Sci. USA. – 2001. – Vol. 98. – P. 13884-13888.
104. Wegmann T.G., Lin H., Guilbert L., Mosmann T.R. Bidirectional cytokine interactions in the maternal-fetal relationship: is successful pregnancy a TH2 phenomenon? // Immunol. Today. – 1993. – Vol. 14. – P. 353-356.
105. Wei J., Satomi M., Negishi Y., Matsumura Y., Miura A., Nishi Y., Asakura H., Takeshita T. Effect of sera on the adhesion of natural killer cells to the endothelium in severe pre-eclampsia // J. Obstet. Gynaecol. Res. – 2006. – Vol. 32, N 5. – P. 443-448.
106. Wojnowski L., Zimmer A.M., Beck T.W., Hahn H., Bernal R., Rapp U.R., Zimmer A. Endothelial apoptosis in Braf-deficient mice // Nat. Genet. – 1997. – Vol. 16. – P. 293-297.
107. Wulff C., Dickson S.E., Wilson H., Wiegand S.J. Hemochorial placentation in the primate: expression of vascular endothelial growth factor, angiopoietins and their receptors throughout pregnancy // Biol. Reprod. – 2002. – Vol. 66. – P. 802-812.
108. Yamamoto T., Geshi Y., Kuno S., Kase N., Mori H. Anti-endothelial cell antibody in preeclampsia: clinical findings and serum cytotoxicity to endothelial cell // Nihon Rinsho Meneki Gakkai Kaishi. – 1998. – Vol. 21. – P. 191-197.
109. Yasuda M., Umemura S., Osamura R.Y., Kenjo T., Tsutsumi Y. Apoptotic cells in the human endometrium and placental villi, pitfalls in applying the TUNEL method // Arch. Histol. Cytol. – 1995. – Vol. 58. – P. 185-190.
110. Zhang E.G., Smith S.K., Baker P.N., Jones D.S. The regulation and localisation of angiopoietin-1,-2 and their receptor Tie2 in normal and pathologic human placentae // Mol. Med. – 2001. – N 7. – P. 624-635.
Рецензия
Для цитирования:
Соколов Д.И. ИММУНОЛОГИЧЕСКИЕ МЕХАНИЗМЫ КОНТРОЛЯ АПОПТОЗА ПРИ РАЗВИТИИ ПЛАЦЕНТЫ. Медицинская иммунология. 2008;10(2-3):125-138. https://doi.org/10.15789/1563-0625-2008-2-3-125-138
For citation:
Sokolov D.I. IMMUNOLOGICAL MECHANISMS OF APOPTOSIS IN PLACENTAL DEVELOPMENT. Medical Immunology (Russia). 2008;10(2-3):125-138. (In Russ.) https://doi.org/10.15789/1563-0625-2008-2-3-125-138