International journal of molecular sciences · 2026
Beyond Shedding: Conserved Retention of ZAN After the Acrosome Reaction Across Rabbit, Boar, and Bull Sperm.
СтатьяНазвание и аннотация: Перевод пока не подготовлен
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Hernández-Falcó Miranda, Díaz-Fuster Lucía, Ferrer-Cortés Núria, Robles-Gómez Laura, Sáez-Espinosa Paula, Gómez-Torres María José
Аннотация
Zonadhesin (ZAN) is a sperm protein currently known to mediate binding to the oocyte zona pellucida. Although its localization has been described in ejaculated and capacitated spermatozoa from mice, pigs, and rabbits, its distribution following the acrosome reaction remains poorly understood. Here, we characterized the localization of ZAN in rabbit, boar, and bull spermatozoa under in vitro conditions designed to mimic early fertilization events. Ejaculated spermatozoa, spermatozoa selected by swim-up in capacitation medium and spermatozoa subjected to acrosome reaction induction were analyzed. Immunofluorescence was performed using an antibody targeting a domain of ZAN distinct from the previously studied domain, together with PNA-FITC to assess acrosomal status; protein abundance was assessed by quantitative LC-MS/MS. ZAN was detected mostly in the anterior region of intact spermatozoa, consistent with previous reports, but the distinct epitope also revealed post-acrosomal localization. Species-specific patterns were observed in intact spermatozoa, whereas following the acrosome reaction, ZAN was consistently detected in the post-acrosomal region. These findings identify a previously unrecognized post-acrosomal distribution of ZAN and suggest that this may contribute not only to sperm-ZP binding but also to later stages of fertilization, including sperm-oolemma interaction and membrane fusion.