From placenta to the foetus: a systematic review of in vitro models of stress- and inflammation-induced depression in pregnancy

IF 9.6 1区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Molecular Psychiatry Pub Date : 2024-12-05 DOI:10.1038/s41380-024-02866-1
Madeline Kirkpatrick, Gargi Mandal, Ismail Elhadidy, Nicole Mariani, Kristi Priestley, Carmine M. Pariante, Alessandra Borsini
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Abstract

Background

Depression in pregnancy can increase vulnerability for psychiatric disorders in the offspring, likely via the transfer of heightened maternal cortisol and cytokines to the in-utero environment. However, the precise cellular and molecular mechanisms, are largely unclear. Animal studies can represent this complex pathophysiology at a systemic level but are expensive and ethically challenging. While simpler, in vitro models offer high-throughput opportunities. Therefore, this systematic review integrates findings of in vitro models relevant to depression in pregnancy, to generate novel hypotheses and targets for intervention.

Methods

The systematic analysis covered studies investigating glucocorticoid or cytokine challenges on placental or foetal neural progenitor cells (NPCs), with or without co-treatment with sex hormones.

Results

Of the 50 included studies, 11 used placental cells and 39 NPCs; surprisingly, only one used a combination of oestrogen and cortisol, and no study combined placental cells and NPCs. In placental cells, cortisol or cytokines decreased nutrient transporter expression and steroidogenic enzyme activity, and increased cytokine production. NPCs exhibited decreases in proliferation and differentiation, via specific molecular pathways, namely, inhibition of hedgehog signalling and activation of kynurenine pathway. In these cells, studies also highlighted epigenetic priming of stress and inflammatory pathways.

Conclusions

Overall, results suggest that stress and inflammation not only detrimentally impact placental regulation of nutrients and hormones to the foetus, but also activate downstream pathways through increased inflammation in the placenta, ultimately eliciting adverse effects on foetal neurogenesis. Future research should investigate how sex hormones regulate these mechanisms, with the aim of developing targeted therapeutic approaches for depression in pregnancy.

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从胎盘到胎儿:妊娠期应激和炎症诱导的抑郁体外模型的系统综述
背景怀孕期间的抑郁可能通过母体皮质醇和细胞因子向子宫内环境的转移而增加后代患精神疾病的脆弱性。然而,精确的细胞和分子机制在很大程度上是不清楚的。动物研究可以在系统水平上代表这种复杂的病理生理,但成本高昂,而且在伦理上具有挑战性。虽然更简单,但体外模型提供了高通量的机会。因此,本系统综述整合了与妊娠期抑郁相关的体外模型的发现,以产生新的假设和干预目标。方法系统分析研究糖皮质激素或细胞因子对胎盘或胎儿神经祖细胞(npc)的影响,并与性激素联合或不联合处理。结果纳入的50项研究中,11项使用胎盘细胞,39项使用npc;令人惊讶的是,只有一项研究将雌激素和皮质醇结合使用,没有一项研究将胎盘细胞和npc结合使用。在胎盘细胞中,皮质醇或细胞因子降低了营养转运蛋白的表达和类固醇生成酶的活性,并增加了细胞因子的产生。npc表现出增殖和分化的减少,通过特定的分子途径,即抑制刺猬信号传导和激活犬尿氨酸途径。在这些细胞中,研究还强调了应激和炎症途径的表观遗传启动。综上所述,应激和炎症不仅会影响胎盘对胎儿的营养和激素的调节,还会通过胎盘炎症的增加激活下游通路,最终对胎儿神经发生产生不利影响。未来的研究应该探究性激素如何调节这些机制,以开发针对妊娠抑郁症的靶向治疗方法。
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来源期刊
Molecular Psychiatry
Molecular Psychiatry 医学-精神病学
CiteScore
20.50
自引率
4.50%
发文量
459
审稿时长
4-8 weeks
期刊介绍: Molecular Psychiatry focuses on publishing research that aims to uncover the biological mechanisms behind psychiatric disorders and their treatment. The journal emphasizes studies that bridge pre-clinical and clinical research, covering cellular, molecular, integrative, clinical, imaging, and psychopharmacology levels.
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