| Description: |
Coelomocytes in the Holothuroidea are traditionally identified according to their morphology through light, fluorescence, or electron microscopy. Former studies have typically used only one method, with few works combining two or more approaches. Studies using cytocentrifugation to study these cells are scarcer. Thus, for the first time, an integrative approach was used to compare coelomocytes in Holothuroidea. This approach consisted of living and stained cells, scanning electron microscopy (for spherule cells), and accurate morphometric analyses. Specifically, we used specimens of Holothuria grisea, Holothuriaarenicola, and Holothuriatubulosa to test whether cytocentrifugation could be valuable in comparative studies with coelomocytes, whether an integrative approach could help to understand spherule cell diversity, and whether closely related species, even those having distinct geographic distributions and ecological requirements, would have a similar population of coelomocytes. Our results showed seven distinct cell types in these species, including phagocytes, fusiform cells, morula cells, acidophilic spherulocytes, spherulocytes, progenitor cells, and crystal cells. Total and differential cell counts, along with morphometric parameters, were similar among species. Morphometric analyses of spherule cells revealed consistent differences among the diameter of their cytoplasmic spherules, as well as a set of different morphotypes in acidophilic spherulocytes and spherulocytes. Cytospin preparations proved to be quite useful because they provided constant morphological and morphometric data, allowing accurate identification of the cell types and comparisons among species. Moreover, this study highlighted (1) that the spherule diameter is a good parameter to separate spherule cells and (2) a putative maturation process to acidophilic spherulocytes and spherulocytes. Lastly, we showed that the cells of these species are very similar, regardless of their geographic distribution and ecology. Thus, our work ... |