Laboratory of Translational Perinatology, University of Regensburg, Biopark 1-3, D-93053, Regensburg, Germany.
University Department of Obstetrics and Gynecology, Clinic St. Hedwig of The Order of St. John, University of Regensburg, Steinmetzstr. 1-3, D-93049, Regensburg, Germany.
Semin Immunopathol. 2024 Aug 12;46(3-4):11. doi: 10.1007/s00281-024-01021-w.
Throughout the individual's reproductive period of life the ovary undergoes continues changes, including cyclic processes of cell death, tissue regeneration, proliferation, and vascularization. Tissue-resident leucocytes particularly macrophages, play a crucial role in shaping ovarian function and maintaining homeostasis. Macrophages crucially promote angiogenesis in the follicles and corpora lutea, thereby supporting steroidogenesis. Recent research on macrophage origins and early tissue seeding has unveiled significant insights into their role in early organogenesis, e.g. in the testis. Here, we review evidence about the prenatal ovarian seeding of leucocytes, primarily macrophages with angiogenic profiles, and its connection to gametogenesis. In the prenatal ovary, germ cells proliferate, form cysts, and undergo changes that, following waves of apoptosis, give rice to the oocytes contained in primordial follicles. These follicles constitute the ovarian reserve that lasts throughout the female's reproductive life. Simultaneously, yolk-sac-derived primitive macrophages colonizing the early ovary are gradually replaced or outnumbered by monocyte-derived fetal macrophages. However, the cues indicating how macrophage colonization and follicle assembly are related are elusive. Macrophages may contribute to organogenesis by promoting early vasculogenesis. Whether macrophages contribute to ovarian lymphangiogenesis or innervation is still unknown. Ovarian organogenesis and gametogenesis are vulnerable to prenatal insults, potentially programming dysfunction in later life, as observed in polycystic ovary syndrome. Experimental and, more sparsely, epidemiological evidence suggest that adverse stimuli during pregnancy can program defective folliculogenesis or a diminished follicle reserve in the offspring. While the ovary is highly sensitive to inflammation, the involvement of local immune responses in programming ovarian health and disease remains to be thoroughly investigated.
在个体的生殖期,卵巢会发生持续的变化,包括细胞死亡、组织再生、增殖和血管生成的周期性过程。组织驻留的白细胞,特别是巨噬细胞,在塑造卵巢功能和维持内稳态方面发挥着至关重要的作用。巨噬细胞在卵泡和黄体中关键地促进血管生成,从而支持类固醇生成。最近对巨噬细胞起源和早期组织定植的研究揭示了它们在早期器官发生中的作用的重要见解,例如在睾丸中。在这里,我们回顾了关于白细胞(主要是具有血管生成特征的巨噬细胞)在产前卵巢定殖及其与配子发生的关系的证据。在产前卵巢中,生殖细胞增殖、形成囊泡,并经历一系列变化,随后发生凋亡,产生包含在原始卵泡中的卵子。这些卵泡构成了女性生殖寿命中持续存在的卵巢储备。同时,卵黄囊衍生的原始巨噬细胞定植早期卵巢,逐渐被单核细胞衍生的胎儿巨噬细胞取代或超过。然而,指示巨噬细胞定植和卵泡组装之间关系的线索仍然难以捉摸。巨噬细胞可能通过促进早期血管生成来促进器官发生。巨噬细胞是否有助于卵巢淋巴管生成或神经支配仍不清楚。卵巢器官发生和配子发生容易受到产前损伤的影响,可能会在以后的生活中导致功能障碍,如多囊卵巢综合征中观察到的那样。实验性的、更稀疏的流行病学证据表明,怀孕期间的不利刺激可以导致后代的卵泡发生缺陷或卵泡储备减少。虽然卵巢对炎症高度敏感,但局部免疫反应在编程卵巢健康和疾病中的参与仍有待深入研究。