In vitroproliferation ofMytilus edulismale germ cell progenitors

Abstract

AbstractOur understanding of basic cellular processes has mostly been provided by mammalian cell culture, and by some non-mammalian vertebrate and few invertebrate cell culture models. Developing reliable culture conditions for non-model organisms is essential to allow investigation of more unusual cellular processes. Here, we investigate how cells isolated from different tissues of the marine musselMytilus edulisthrive and survivein vitroin the hope of establishing a suitable laboratory model for the investigation of cellular mechanisms specific to these bivalve mollusks. We found that cells dissociated from male mantle tissue attached to the culture vessels and proliferated wellin vitro, whereas all other cell types, although remaining viable, did not maintain divisions over three to four weeks in culture. We used antibodies against the germ-line marker DEAD-box helicase 4 (DDX4), also known as VASA, and the epithelial cell marker cytokeratin to distinguish different cell types in culture. DDX4-positive cells were the only cells that significantly proliferated in culture, and only from male tissue samples. Overall, the culture conditions described here allow an efficient selection of male germ cells that could be used to study specific cellular mechanismsin vitro.