Role of GPR55 receptor in bovine sperm capacitation

IF 3.4 2区 医学 Q1 ANDROLOGY Andrology Pub Date : 2025-01-03 DOI:10.1111/andr.13823
Raquel Lottero-Leconte, Angela Lara, Jessica Plaza, Camila Arroyo-Salvo, María Eugenia Bogetti, Amada Eugenia Ynsaurralde Rivolta, Franco Dellavalle, Fiamma Sengiali, Pablo Cetica, Sofía Rio, Lucia Zalazar, Andreína Cesari, Marcelo Miragaya, Sergio Morado, Silvina Perez-Martinez
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Abstract

Background

Endocannabinoids like anandamide (AEA), among other lipids, are recognized signaling molecules that participate in reproductive events.

Objectives

Our aims were to characterize orphan G protein-coupled receptor (GPR55) presence; investigate GPR55 activation by AEA and determine GPR55 role in the bovine sperm function.

Materials and methods

GPR55 presence was assessed by immunocytochemistry. Protein kinase A (pPKA) and PKC (pPKC) substrates, pERK1/2, G/F-actin were determined by Western blotting, activation of RAC-1 by pull-down assay, F-actin and acrosomal exocytosis by fluorescence microscopy, sperm motility by optic microscopy and computer-aided sperm analysis and fertilizing ability by in vitro fertilization (IVF).

Results

We detected GPR55 in spermatozoa at T0, after incubation in non-capacitating and capacitating (presence of AEA) conditions and upon release from oviductal epithelia. AEA induced an increase in pPKA and pPKC, while CID16020046 (CID), selective GPR55 antagonist, prevented this effect. Incubation with H89, PKA inhibitor, significantly decreased pPKC, while Gö6983, a PKC inhibitor, partially reduced pPKA. pPKA remained elevated at 15- and 45-min incubation, while pPKC decreased at 15 and increased at 45 min. CID prevented pPKC increase at 5 and 45 min and decreased pPKA at 45 min. RAC-1 and F-actin increase induced by AEA was prevented by CID. Variations in two progressive motility kinematic parameters were observed with AEA and/or CID. Sperm pretreatment with AEA increased the rate of cleaved embryos and CID prevented this effect.

Discussion

We demonstrated that GPR55 activation by AEA induces time-dependent signaling pathways involving pPKA and pPKC during bovine sperm capacitation. AEA regulates actin polymerization through GPR55 activation, suggesting the receptor participates in cytoskeleton remodeling, and yielded higher IVF rates. Also, sperm pre-incubation with molecules like AEA involved in capacitation could improve the embryo development.

Conclusion

We have demonstrated GPR55 presence in bovine spermatozoa. The regulation of PKA and PKC and of molecules associated with cytoskeletal dynamics, such as RAC-1 and actin, by GPR55 is closely related to sperm motility and acrosomal exocytosis.

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GPR55受体在牛精子获能中的作用。
背景:内源性大麻素(Endocannabinoids, anandamide, AEA)和其他脂质一样,是公认的参与生殖活动的信号分子。目的:我们的目的是表征孤儿G蛋白偶联受体(GPR55)的存在;用AEA研究GPR55的活化,并确定GPR55在牛精子功能中的作用。材料与方法:免疫细胞化学检测GPR55的存在。蛋白激酶A (pPKA)和PKC (pPKC)底物、pERK1/2、G/ f -肌动蛋白采用Western blotting检测,RAC-1激活采用拉下法检测,f -肌动蛋白和顶体胞泌量采用荧光显微镜检测,精子活力采用光学显微镜检测,计算机辅助精子分析采用体外受精(IVF)检测受精能力。结果:我们在T0、非能性和能性条件下(存在AEA)孵育后以及从输卵管上皮释放后的精子中检测到GPR55。AEA诱导pPKA和pPKC升高,而选择性GPR55拮抗剂CID16020046 (CID)阻止了这一作用。PKA抑制剂H89能显著降低pPKC, PKC抑制剂Gö6983能部分降低pPKA。pPKA在15和45 min时保持升高,而pPKC在15 min时降低,45 min时升高。CID阻止pPKC在5和45 min时升高,并在45 min时降低pPKA。在AEA和/或CID中观察到两个进行性运动运动学参数的变化。AEA预处理能提高精子的卵裂率,而CID能抑制这一作用。讨论:我们证明了在牛精子获能过程中,AEA激活GPR55诱导了包括pPKA和pPKC在内的时间依赖性信号通路。AEA通过激活GPR55调控肌动蛋白聚合,提示该受体参与细胞骨架重塑,提高了体外受精成功率。此外,与参与获能的AEA等分子一起对精子进行预孵育可以改善胚胎的发育。结论:牛精子中存在GPR55。GPR55对PKA和PKC以及与细胞骨架动力学相关的分子如RAC-1和肌动蛋白的调控与精子运动和顶体胞外分泌密切相关。
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来源期刊
Andrology
Andrology ANDROLOGY-
CiteScore
9.10
自引率
6.70%
发文量
200
期刊介绍: Andrology is the study of the male reproductive system and other male gender related health issues. Andrology deals with basic and clinical aspects of the male reproductive system (gonads, endocrine and accessory organs) in all species, including the diagnosis and treatment of medical problems associated with sexual development, infertility, sexual dysfunction, sex hormone action and other urological problems. In medicine, Andrology as a specialty is a recent development, as it had previously been considered a subspecialty of urology or endocrinology
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