Cormier Nathaly, McGlone John J, Leszyk John, Hardy Daniel M
Department of Cell Biology & Biochemistry, Texas Tech University Health Sciences Center, Lubbock, Texas, United States of America.
Department of Animal and Food Sciences, Texas Tech University, Lubbock, Texas, United States of America.
PLoS One. 2018 Jan 17;13(1):e0190891. doi: 10.1371/journal.pone.0190891. eCollection 2018.
Sperm competence in animal fertilization requires the collective activities of numerous sperm-specific proteins that are typically alloimmunogenic in females. Consequently, sperm membrane alloantigens are potential targets for contraceptives that act by blocking the proteins' functions in gamete interactions. Here we used a targeted proteomics approach to identify the major alloantigens in swine sperm membranes and lipid rafts, and thereby systematically defined the repertoire of these sperm-specific proteins in a single species. Gilts with high alloantibody reactivity to proteins in sperm membranes or lipid rafts produced fewer offspring (73% decrease) than adjuvant-only or nonimmune control animals. Alloantisera recognized more than 20 potentially unique sperm membrane proteins and five sperm lipid raft proteins resolved on two-dimensional immunoblots with or without prior enrichment by anion exchange chromatography. Dominant sperm membrane alloantigens identified by mass spectrometry included the ADAMs fertilin α, fertilin ß, and cyritestin. Less abundant alloantigens included ATP synthase F1 β subunit, myo-inositol monophosphatase-1, and zymogen granule membrane glycoprotein-2. Immunodominant sperm lipid raft alloantigens included SAMP14, lymphocyte antigen 6K, and the epididymal sperm protein E12. Of the fifteen unique membrane alloantigens identified, eleven were known sperm-specific proteins with uncertain functions in fertilization, and four were not previously suspected to exist as sperm-specific isoforms. De novo sequences of tryptic peptides from sperm membrane alloantigen "M6" displayed no evident homology to known proteins, so is a newly discovered sperm-specific gene product in swine. We conclude that alloimmunizing gilts with sperm membranes or lipid rafts evokes formation of antibodies to a relatively small number of dominant alloantigens that include known and novel sperm-specific proteins with possible functions in fertilization and potential utility as targets for immunocontraception.
动物受精过程中的精子受精能力需要众多精子特异性蛋白的协同作用,而这些蛋白在雌性动物体内通常具有同种免疫原性。因此,精子膜同种抗原是避孕药的潜在作用靶点,这类避孕药通过阻断蛋白在配子相互作用中的功能来发挥作用。在此,我们采用靶向蛋白质组学方法来鉴定猪精子膜和脂筏中的主要同种抗原,从而系统地确定了单一物种中这些精子特异性蛋白的全部组成。对精子膜或脂筏中的蛋白具有高同种抗体反应性的后备母猪,其产仔数比仅注射佐剂的动物或非免疫对照动物少(减少73%)。同种抗血清在二维免疫印迹上识别出20多种潜在独特的精子膜蛋白和5种精子脂筏蛋白,无论是否事先通过阴离子交换色谱法进行富集。通过质谱鉴定出的主要精子膜同种抗原包括ADAMs受精素α、受精素β和cyritestin。含量较少的同种抗原包括ATP合酶F1β亚基、肌醇单磷酸酶-1和酶原颗粒膜糖蛋白-2。免疫显性精子脂筏同种抗原包括SAMP14、淋巴细胞抗原6K和附睾精子蛋白E12。在鉴定出的15种独特膜同种抗原中,有11种是已知的精子特异性蛋白,其在受精中的功能尚不确定,另外4种以前未被怀疑以精子特异性异构体的形式存在。精子膜同种抗原“M6”的胰蛋白酶肽段的从头序列与已知蛋白没有明显同源性,因此是猪中新发现的精子特异性基因产物。我们得出结论,用精子膜或脂筏对后备母猪进行同种免疫会诱发针对相对少量主要同种抗原的抗体形成,这些抗原包括已知的和新的精子特异性蛋白,它们在受精中可能具有功能,并且作为免疫避孕的靶点具有潜在用途。