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Fetal exposure to oral pathogens and subsequent risk for neonatal intensive care admission.胎儿暴露于口腔病原体及随后入住新生儿重症监护病房的风险。
J Periodontol. 2009 Jun;80(6):878-83. doi: 10.1902/jop.2009.080642.
2
Effect of periodontal disease treatment during pregnancy on preterm birth incidence: a metaanalysis of randomized trials.孕期牙周病治疗对早产发生率的影响:随机试验的荟萃分析
Am J Obstet Gynecol. 2009 Mar;200(3):225-32. doi: 10.1016/j.ajog.2008.09.020.
3
Bacterial infection promotes DNA hypermethylation.细菌感染会促进DNA高度甲基化。
J Dent Res. 2007 Feb;86(2):169-74. doi: 10.1177/154405910708600212.
4
Expanding the COL7A1 mutation database: novel and recurrent mutations and unusual genotype-phenotype constellations in 41 patients with dystrophic epidermolysis bullosa.扩大COL7A1突变数据库:41例营养不良性大疱性表皮松解症患者中的新突变和复发性突变以及异常的基因型-表型组合
J Invest Dermatol. 2006 May;126(5):1006-12. doi: 10.1038/sj.jid.5700219.
5
Destruction of the main olfactory epithelium reduces female sexual behavior and olfactory investigation in female mice.主要嗅觉上皮的破坏会降低雌性小鼠的性行为和嗅觉探究能力。
Chem Senses. 2006 May;31(4):315-23. doi: 10.1093/chemse/bjj035. Epub 2006 Feb 16.
6
Olfactory loss in aging.衰老过程中的嗅觉丧失。
Sci Aging Knowledge Environ. 2006 Feb 8;2006(5):pe6. doi: 10.1126/sageke.2006.5.pe6.
7
Effects of maternal Campylobacter rectus infection on murine placenta, fetal and neonatal survival, and brain development.母体直肠弯曲杆菌感染对小鼠胎盘、胎儿及新生儿存活以及脑发育的影响。
J Periodontol. 2005 Nov;76(11 Suppl):2133-43. doi: 10.1902/jop.2005.76.11-S.2133.
8
Unbalanced placental expression of imprinted genes in human intrauterine growth restriction.人类宫内生长受限中印迹基因的胎盘表达失衡。
Placenta. 2006 Jun-Jul;27(6-7):540-9. doi: 10.1016/j.placenta.2005.07.004. Epub 2005 Aug 24.
9
Campylobacter rectus mediates growth restriction in pregnant mice.直肠弯曲杆菌介导孕鼠生长受限。
J Periodontol. 2005 Apr;76(4):551-7. doi: 10.1902/jop.2005.76.4.551.
10
Overexpression of the soluble vascular endothelial growth factor receptor in preeclamptic patients: pathophysiological consequences.可溶性血管内皮生长因子受体在子痫前期患者中的过表达:病理生理后果
J Clin Endocrinol Metab. 2003 Nov;88(11):5555-63. doi: 10.1210/jc.2003-030528.

感染诱导的宫内生长受限模型中小鼠胎盘基因表达的改变:微阵列分析。

Altered gene expression in murine placentas in an infection-induced intrauterine growth restriction model: a microarray analysis.

机构信息

University of Athens, 2 Thiron, 11527 Goudi, Athens, Greece.

出版信息

J Reprod Immunol. 2010 Jun;85(2):140-8. doi: 10.1016/j.jri.2010.04.001. Epub 2010 May 16.

DOI:10.1016/j.jri.2010.04.001
PMID:20478622
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2904600/
Abstract

The biological mechanisms leading to incomplete intrauterine growth are not completely elucidated and few studies have investigated infection-mediated growth restriction. In this investigation we report the alterations induced by maternal infectious challenge in placental gene expression patterns using a murine model. Pregnant dams were challenged at day E7.5 with the oral human pathogen Campylobacter rectus to elicit fetal growth restriction. At embryonic day E16.5 placentas were collected to compare placental gene expression patterns from normal fetuses of unchallenged dams and growth restricted fetuses from infected dams. Differential gene expression patterns were determined using Agilent Oligo array (G4121A) with a false discovery rate of P<0.05 and pathway analyses were performed. Seventy-four genes were differentially expressed during infection-mediated growth restriction with 9 genes significantly up-regulated, indicating that the effects of maternal infection on gene expression were predominantly suppressive. Pathway analyses indicated that 46 of the 65 genes that were significantly down-regulated were associated with placental/fetal development, and 26 of those were imprinted genes. Among the 9 genes that were up-regulated, 4 are involved in oxygen supply to the fetus and the development of the vascular system. Microarray analysis demonstrated that in the pregnant mouse model, maternal infection that induced growth restriction was associated with down-regulated placental expression of critical growth and developmental related genes, including many imprinted genes. These findings may have significant implications for our understanding of the mechanisms underlying infection-associated human fetal growth restriction and the role of differential placental expression of imprinted genes in fetal growth.

摘要

导致宫内生长不全的生物学机制尚未完全阐明,很少有研究调查感染介导的生长受限。在本研究中,我们使用小鼠模型报告了母体感染挑战对胎盘基因表达模式的诱导变化。在 E7.5 天,用口服人类病原体弯曲杆菌rectus 感染怀孕的母鼠,以引发胎儿生长受限。在胚胎 E16.5 天收集胎盘,以比较未受感染母鼠的正常胎儿和感染母鼠的生长受限胎儿的胎盘基因表达模式。使用 Agilent Oligo 阵列 (G4121A) 确定差异表达基因,假发现率为 P<0.05,并进行通路分析。在感染介导的生长受限期间,有 74 个基因的表达存在差异,其中 9 个基因显著上调,表明母体感染对基因表达的影响主要是抑制性的。通路分析表明,在 65 个显著下调的基因中,有 46 个与胎盘/胎儿发育有关,其中 26 个是印迹基因。在上调的 9 个基因中,有 4 个参与胎儿的氧气供应和血管系统的发育。微阵列分析表明,在怀孕的小鼠模型中,诱导生长受限的母体感染与关键生长和发育相关基因的胎盘表达下调有关,包括许多印迹基因。这些发现可能对我们理解感染相关人类胎儿生长受限的机制以及印迹基因在胎儿生长中的差异表达的作用具有重要意义。