THE NOTCH SIGNALING PATHWAY IN THE HUMAN PLACENTA DURING PHYSIOLOGICAL AND COMPLICATED PREGNANCY
- Authors: Pavlov K.A.1, Dubova E.A.1, Shchegolev A.I.1
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Affiliations:
- Academician V.I. Kulakov Research Center of Obstetrics, Gynecology, and Perinatology, Ministry of Health of Russia
- Issue: No 2 (2015)
- Pages: 5-11
- Section: Articles
- URL: https://journals.eco-vector.com/0300-9092/article/view/247344
- ID: 247344
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About the authors
Konstantin A. Pavlov
Academician V.I. Kulakov Research Center of Obstetrics, Gynecology, and Perinatology, Ministry of Health of Russia
Email: kpavlov@oparina4.ru
PhD in medicine, member of the 2nd Pathanatomy department 117997, Russia, Moscow, Ac. Oparina str. 4
Elena A. Dubova
Academician V.I. Kulakov Research Center of Obstetrics, Gynecology, and Perinatology, Ministry of Health of Russia
Email: e_dubova@oparina4.ru
PhD in medicine, member of the 2nd Pathanatomy department 117997, Russia, Moscow, Ac. Oparina str. 4
AІexander I. Shchegolev
Academician V.I. Kulakov Research Center of Obstetrics, Gynecology, and Perinatology, Ministry of Health of Russia
Email: ashegolev@oparina4.ru
PhD, Chief of pathology Department 117997, Russia, Moscow, Ac. Oparina str. 4
References
- Morgan T. The theory of the gene. Am. Naturalist. 1917; 51: 513-44.
- Artavanis-Tsakonas S., Rand M.D., Lake R.J. Notch signaling: cell fate control and signal integration in development. Science. 1999; 284(5415): 770-6.
- Kopan R., Hagan M.X. The canonical Notch signaling pathway: unfolding the activation mechanism. Cell. 2009; 137(2): 216-33.
- D’Souza B., Meloty-KapeBa L., Weinmaster G. Canonical and non-canonical Notch ligands. Curr. Top. Dev. Biol. 2010; 92: 73-129.
- Radtke F., Raj K. The role of Notch in tumorigenesis: oncogene or tumour suppressor? Nat. Rev. Cancer. 2003; 3(10): 756-67.
- Pannuti A., Foreman K., Rizzo P., Osipo C., Golde T., Osborne B. et al. Targeting Notch to target cancer stem cells. Clin. Cancer Res. 2010; 16(12): 3141-52.
- Limbourg A., Ploom M., Elligsen D., Sorensen I., Ziegelhoeffer T., Gossler A. et al. Notch ligand Delta-like 1 is essential for postnatal arteriogenesis. Circ. Res. 2007; 100(3): 363-71.
- Kovall R.A., Blacklow S.C. Mechanistic insights into Notch receptor signaling from structural and biochemical studies. Curr. Top. Dev. Biol. 2010; 92: 31-71.
- Wharton K.A., Johansen K.M., Xu T., Artavanis-Tsakonas S. Nucleotide sequence from the neurogenic locus Notch implies a gene product that shares homology with proteins containing EGF-like repeats. Cell. 1985; 43(3, Pt 2): 567-81.
- Rebay I., Fehon R.G., Artavanis-Tsakonas S. Specific truncations of Drosophila Notch define dominant activated and dominant negative forms of the receptor. Cell. 1993; 74(2): 319-29.
- Greenwald I. Structure/function studies of lin-12/Notch proteins. Curr. Opin. Genet. Dev. 1994; 4(4): 556-62.
- Andersson E.R., Sandberg R., Lendahl U. Notch signaling: simplicity in design, versatility in function. Development. 2011; 138(17): 3593-612.
- Pan D, Rubin G.M. Kuzbanian controls proteolytic processing of Notch and mediates lateral inhibition during Drosophila and vertebrate neurogenesis. Cell. 1997; 90(2): 271-80.
- Schroeter E.H., Kisslinger J.A., Kopan R. Notch-1 signalling requires ligand-induced proteolytic release of intracellular domain. Nature. 1998; 393(6683): 382-6.
- De Strooper B., Annaert W, Cupers P., Saftig P., Craessaerts K., Mumm J.S. et al. A presenilin-1-dependent gamma-secretase-like protease mediates release of Notch intracellular domain. Nature. 1999; 398(6727): 518-22.
- Schweisguth F. Regulation of Notch signaling activity. Curr. Biol. 2004; 14(3): R129-38.
- Lai E.C. Notch signaling: control of cell communication and cell fate. Development. 2004; 131(5): 965-73.
- Gazave E., Lapebie P., Richards G.S., Brunet F., Ereskovsky A.V., Degnan B. M. et al. Origin and evolution of the Notch signalling pathway: an overview from eukaryotic genomes. BMC Evol. Biol. 2009; 9: 249.
- Fortini M.E. Notch and presenilin: a proteolytic mechanism emerges. Curr. Opin. Cell Biol. 2001; 13(5): 627-34.
- Ma Q.H., Futagawa T., Yang W.L., Jiang X.D., Zeng L., Takeda Y. et al. A TAG1-APP signalling pathway through Fe65 negatively modulates neurogenesis. Nat. Cell Biol. 2008; 10(3): 283-94.
- Lu F.M., Lux S.E. Constitutively active human Notch1 binds to the transcription factor CBF1 and stimulates transcription through a promoter containing a CBF1-responsive element. Proc. Natl. Acad. Sci. USA. 1996; 93(11): 5663-7.
- PetcherskiA.G., Kimble J. LAG-3 is a putative transcriptional activator in the C. elegans Notch pathway. Nature. 2000; 405(6784): 364-8.
- Martinez Arias A., Zecchini V., Brennan K. CSL-independent Notch signalling: a checkpoint in cell fate decisions during development? Curr. Opin. Genet. Dev. 2002; 12(5): 524-33.
- Oswald F., Winkler M., Cao Y., Astrahantseff K., Bourteele S., Knochel W. et al. RBP-Jkappa/SHARP recruits CtIP/CtBP corepressors to silence Notch target genes. Mol. Cell. Biol. 2005; 25(23): 10379-90.
- Wu L., Aster J. C., Blacklow S.C., Lake R., Artavanis-Tsakonas S., Griffin J.D. MAML1, a human homologue of Drosophila mastermind, is a transcriptional co-activator for NOTCH receptors. Nat. Genet. 2000; 26(4): 484-9.
- Andersen P, Uosaki H., Shenje L.T., Kwon C. Non-canonical Notch signaling: emerging role and mechanism. Trends Cell Biol. 2012; 22(5): 257-65.
- Fiuza U.M., Arias A.M. Cell and molecular biology of Notch. J. Endocrinol. 2007; 194(3): 459-74.
- Afshar Y., Miele L., Fazleabas A.T. Notch1 is regulated by chorionic gonadotropin and progesterone in endometrial stromal cells and modulates decidualization in primates. Endocrinology. 2012; 153(6): 2884-96.
- De Falco M., Cobellis L., Giraldi D., Mastrogiacomo A., Perna A., Colacurci N. et al. Expression and distribution of Notch protein members in human placenta throughout pregnancy. Placenta. 2007; 28(2-3): 118-26.
- Gasperowicz M., Otto F The Notch signalling pathway in the development of the mouse placenta. Placenta. 2008; 29(8): 651-9.
- Nakayama H., Liu Y., Stifani S., Cross J.C. Developmental restriction of Mash-2 expression in trophoblast correlates with potential activation of the notch-2 pathway. Dev. Genet. 1997; 21(1): 21-30.
- Lunghi L., Ferretti M.E., Medici S., Biondi C., Vesce F. Control of human trophoblast function. Reprod. Biol. Endocrinol. 2007; 5: 6.
- Павлов К.А., Дубова Е.А., Щеголев А.И. Фетоплацентарный ангиогенез при нормальной беременности: роль плацентарного фактора роста и ангиопоэтинов. Акушерство и гинекология. 2010; 6: 10-5.
- Павлов К.А., Дубова Е.А., Щеголев А.И. Фетоплацентарный ангиогенез при нормальной беременности: роль сосудистого эндотелиального фактора роста. Акушерство и гинекология. 2011; 3: 11-6.
- Zhou Y., Fisher S.J., Janatpour M., Genbacev O., Dejana E., Wheelock M. et al. Human cytotrophoblasts adopt a vascular phenotype as they differentiate. A strategy for successful endovascular invasion? J. Clin. Invest. 1997; 99(9): 2139-51.
- Zhou Y., Damsky C.H., Fisher S.J. Preeclampsia is associated with failure of human cytotrophoblasts to mimic a vascular adhesion phenotype. One cause of defective endovascular invasion in this syndrome? J. Clin. Invest. 1997; 99(9): 2152-64.
- Norwitz E.R. Defective implantation and placentation: laying the blueprint for pregnancy complications. Reprod. Biomed. Online. 2006; 13(4): 591-9.
- Brosens J.J., Pijnenborg R., Brosens I.A. The myometrial junctional zone spiral arteries in normal and abnormal pregnancies: a review of the literature. Am. J. Obstet. Gynecol. 2002; 187(5): 1416-23.
- Herr F., Schreiner I., Baal N., Pfarrer C., Zygmunt M. Expression patterns of Notch receptors and their ligands Jagged and Delta in human placenta. Placenta. 2011; 32(8): 554-63.
- Hunkapiller N.M., Gasperowicz M., Kapidzic M., Plaks V., Maltepe E., Kitajewski J. et al. A role for Notch signaling in trophoblast endovascular invasion and in the pathogenesis of pre-eclampsia. Development. 2011; 138(14): 2987-98.
- Zhao W.-X., Lin J.-H. Notch signaling pathway and human placenta. Int. J. Med. Sci. 2012; 9: 447-52.
- Sahin Z., Acar N., Ozbey O., Ustunel I., Demir R. Distribution of Notch family proteins in intrauterine growth restriction and hypertension complicated human term placentas. Acta Histochem. 2011; 113(3): 270-6.
- Rizzo P, Miao H., D’Souza G., Osipo C., Song L.L., Yun J. et al. Cross-talk between Notch and the estrogen receptor in breast cancer suggests novel therapeutic approaches. Cancer Res. 2008; 68(13): 5226-35.
- Kume T. Ligand-dependent Notch signaling in vascular formation. Adv. Exp. Med. Biol. 2012; 727: 210-22.
- Cobellis L., Mastrogiacomo A., Federico E., Schettino M. T., De Falco M., Manente L. et al. Distribution of Notch protein members in normal and preeclampsia-complicated placentas. Cell Tissue Res. 2007; 330(3): 527-34.
- Wagener J., Yang W., Kazuschke K., Winterhager E., Gellhaus A. CCN3 regulates proliferation and migration properties in Jeg3 trophoblast cells via ERK1/2, Akt and Notch signalling. Mol. Hum. Reprod. 2013; 19(4): 237-49.
- Fang Y., Yu S., Ma Y., Sun P, Ma D., Ji C. et al. Association of Dll4/Notch and HIF-1a -VEGF signaling in the angiogenesis of missed abortion. PLoS One. 2013; 8(8): e70667.
- Pavlov K.A., Dubova E.A., Shchegolev A.I., Sukhikh G.T. The role of placental Notch signaling pathway disturbances in preeclampsia. Virchows Arch. 2013; 463 (1): 119.
- Founds S.A., Conley Y.P., Lyons-Weiler J.F., Jeyabalan A., Hogge W.A., Conrad K. P Altered global gene expression in first trimester placentas of women destined to develop preeclampsia. Placenta. 2009; 30(1): 15-24.
- Cuman C., Menkhorst E., Winship A., Van Sinderen M., Osianlis T., Rombauts L.J. et al. Fetal-maternal communication: the role of Notch signalling in embryo implantation. Reproduction. 2014; 147(3): R75-86.
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