Laboratorio de Estudios de Interacción Celular en Reproducción y Cáncer, Instituto de Biología y Medicina Experimental (IBYME), Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Fundación IBYME (FIBYME), Buenos Aires C1428ADN, Argentina.
BioAplicada-Laboratorio de Cultivos Celulares y Estudios Especiales, Buenos Aires C1430EYV, Argentina.
Cells. 2021 Dec 29;11(1):102. doi: 10.3390/cells11010102.
Successful mammalian fertilization requires a well-orchestrated sequence of molecular events leading to gamete fusion. Since this interaction involves Ca-dependent adhesion events, the participation of the Ca-dependent cell-cell adhesion proteins Epithelial (E-cad) and Neural (N-cad) cadherin is envisaged. We have previously reported the expression of E-cad and N-cad in human gametes and showed evidence of their involvement in sperm-oocyte adhesion events leading to fertilization. To overcome ethical limitations associated with the use of human gametes in fertilization-related studies, the mouse has been selected worldwide as the experimental model for over 4 decades. Herein, we report a detailed study aimed at characterizing the expression of E-cad and N-cad in murine gametes and their involvement in murine fertilization using specific antibodies and blocking peptides towards both adhesion proteins. E-cad and N-cad protein forms, as well as other members of the adhesion complex, specifically β-catenin and actin, were identified in spermatozoa, cumulus cells and oocytes protein extracts by means of Western immunoblotting. In addition, subcellular localization of these proteins was determined in whole cells using optical fluorescent microscopy. Gamete pre-incubation with anti-E-cad (ECCD-1) or N-cad (H-63) antibodies resulted in decreased ( < 0.05) In Vitro Fertilization (IVF) rates, when using both cumulus-oocytes complexes and cumulus-free oocytes. Moreover, IVF assays done with denuded oocytes and either antibodies or blocking peptides against E-cad and N-cad led to lower ( < 0.05) fertilization rates. When assessing each step, penetration of the cumulus mass was lower ( < 0.05) when spermatozoa were pre-incubated with ECCD-1 or blocking peptides towards E-cad or towards both E- and N-cad. Moreover, sperm-oolemma binding was impaired ( < 0.0005) after sperm pre-incubation with E-cad antibody or blocking peptide towards E-cad, N-cad or both proteins. Finally, sperm-oocyte fusion was lower ( < 0.05) after sperm pre-incubation with either antibody or blocking peptide against E-cad or N-cad. Our studies demonstrate the expression of members of the adherent complex in the murine model, and the use of antibodies and specific peptides revealed E-cad and N-cad participation in mammalian fertilization.
哺乳动物的受精成功需要一系列精心协调的分子事件,导致配子融合。由于这种相互作用涉及 Ca 依赖性粘附事件,因此设想钙依赖性细胞-细胞粘附蛋白上皮(E-cad)和神经(N-cad)钙粘蛋白的参与。我们之前报道了人类配子中 E-cad 和 N-cad 的表达,并证明它们参与了导致受精的精子-卵母细胞粘附事件。为了克服与受精相关研究中使用人类配子相关的伦理限制,老鼠已被全世界选为实验模型超过 4 十年。在此,我们报告了一项详细的研究,旨在使用针对这两种粘附蛋白的特异性抗体和阻断肽,描述 E-cad 和 N-cad 在小鼠配子中的表达及其在小鼠受精中的作用。通过 Western 免疫印迹法,在精子、卵丘细胞和卵母细胞蛋白提取物中鉴定了 E-cad 和 N-cad 蛋白形式以及粘附复合物的其他成员,特异性 β-连环蛋白和肌动蛋白。此外,使用光学荧光显微镜在整个细胞中确定了这些蛋白质的亚细胞定位。用抗 E-cad(ECCD-1)或 N-cad(H-63)抗体预孵育配子会导致体外受精(IVF)率降低(<0.05),无论是使用卵丘-卵母细胞复合物还是卵丘游离卵母细胞。此外,用裸卵母细胞进行的 IVF 测定,以及针对 E-cad 和 N-cad 的抗体或阻断肽,导致更低的(<0.05)受精率。在评估每个步骤时,当精子预先用 ECCD-1 或针对 E-cad 或针对 E-和 N-cad 的阻断肽预孵育时,卵丘质量的穿透率降低(<0.05)。此外,在用 E-cad 抗体或针对 E-cad、N-cad 或两种蛋白质的阻断肽预孵育精子后,精子-卵母细胞结合受到损害(<0.0005)。最后,在用针对 E-cad 或 N-cad 的抗体或阻断肽预孵育精子后,精子-卵母细胞融合率降低(<0.05)。我们的研究表明,在小鼠模型中表达了粘附复合物的成员,并且使用抗体和特异性肽揭示了 E-cad 和 N-cad 参与哺乳动物受精。