到目前为止,卵母细胞活化是一个细胞质封闭的事件,那么细胞核呢?

IF 3.7 3区 生物学 Q1 DEVELOPMENTAL BIOLOGY Reproduction Pub Date : 2024-02-02 Print Date: 2024-03-01 DOI:10.1530/REP-23-0360
Luisa Gioia, Luca Palazzese, Marta Czernik, Domenico Iuso, Helena Fulka, Josef Fulka, Pasqualino Loi
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引用次数: 0

摘要

受精精子会诱导 Ca2+ 振荡模式,这是所有有性生殖动物卵母细胞活化的普遍标志。辅助生殖技术(ART),如卵胞浆内单精子显微注射(ICSI),绕过了这一生理途径;然而,虽然正常的 Ca2+ 释放模式会出现在某些物种中,尤其是人类,但在大多数农场动物中,ICSI 受精卵母细胞的发育必须经过人工激活。与正常的振荡模式不同,大多数人工激活方案会诱发单一的 Ca2+ 峰值,从而影响这些物种中 ICSI 胚胎的正常发育。奇怪的是,用同样的方法激活的二倍体孤雌生殖胚胎却能高频率地正常发育,并在移植到子宫后着床。我们假设,至少在反刍动物的胚胎中,第一个细胞周期晚期的振荡钙波优先以父代前核为目标,对父代核重塑具有根本性的重要作用。我们认为,Ca2+信号是父系基因组完全全能性部署的核心。该领域的研究可突出早期发育中父代基因组重编程时间/机制的不对称性,并对ICSI和克隆等ART产生影响。
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Oocyte activation is a cytoplasm-confined event so far: what about the nucleus?

The fertilizing spermatozoa induce a Ca2+ oscillatory pattern, the universal hallmark of oocyte activation, in all sexually reproducing animals. Assisted reproductive technologies (ARTs) like intracytoplasmic sperm injection (ICSI) bypass the physiological pathway; however, while a normal Ca2+ release pattern occurs in some species, particularly humans, artificial activation is compulsory for ICSI-fertilized oocytes to develop in most farm animals. Unlike the normal oscillatory pattern, most artificial activation protocols induce a single Ca2+ spike, undermining proper ICSI-derived embryo development in these species. Curiously, diploid parthenogenetic embryos activated by the same treatments develop normally at high frequencies and implant upon transfer in the uterus. We hypothesized that, at least in ruminant embryos, the oscillatory calcium waves late in the first cell cycle target preferentially the paternal pronucleus and are fundamentally important for paternal nuclear remodeling. We believe that Ca2+ signaling is central to full totipotency deployment of the paternal genome. Research in this area could highlight the asymmetry between the parental genome reprogramming timing/mechanisms in early development and impact ARTs like ICSI and cloning.

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来源期刊
Reproduction
Reproduction 生物-发育生物学
CiteScore
7.40
自引率
2.60%
发文量
199
审稿时长
4-8 weeks
期刊介绍: Reproduction is the official journal of the Society of Reproduction and Fertility (SRF). It was formed in 2001 when the Society merged its two journals, the Journal of Reproduction and Fertility and Reviews of Reproduction. Reproduction publishes original research articles and topical reviews on the subject of reproductive and developmental biology, and reproductive medicine. The journal will consider publication of high-quality meta-analyses; these should be submitted to the research papers category. The journal considers studies in humans and all animal species, and will publish clinical studies if they advance our understanding of the underlying causes and/or mechanisms of disease. Scientific excellence and broad interest to our readership are the most important criteria during the peer review process. The journal publishes articles that make a clear advance in the field, whether of mechanistic, descriptive or technical focus. Articles that substantiate new or controversial reports are welcomed if they are noteworthy and advance the field. Topics include, but are not limited to, reproductive immunology, reproductive toxicology, stem cells, environmental effects on reproductive potential and health (eg obesity), extracellular vesicles, fertility preservation and epigenetic effects on reproductive and developmental processes.
期刊最新文献
REPRODUCTIVE HEALTH IN TRANS AND GENDER-DIVERSE PATIENTS: Gonadal tissue cryopreservation in transgender and gender-diverse people. IMPACT OF REAL-LIFE ENVIRONMENTAL EXPOSURES ON REPRODUCTION: A contemporary review of machine learning to predict adverse pregnancy outcomes from pharmaceuticals, including DDIs. O-GlcNAc participates in the meiosis of aging oocytes by mediating mitochondrial function. REPRODUCTIVE HEALTH IN TRANS AND GENDER-DIVERSE PATIENTS: Trauma-informed reproductive care for transgender and nonbinary people. SON controls mouse early embryonic development by regulating RNA splicing and histone methylation.
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