Formation of the diverticular lumen that enables oocyte fertilization in katoikogenic scorpions, Heterometrus spinifer and Opistophthalmus boehmi (Scorpionidae).

The structure of diverticula of the female gonads was analyzed in two scorpions from the family Scorpionidae by means of standard microscopic techniques (light microscopy, histochemistry, transmission electron microscopy). In scorpions, the female gonad, termed the ovariuterus, participates in two consecutive processes: oogenesis and embryogenesis. In sexually reproducing scorpions, the ovariuterus is also involved in fertilization. Both scorpions under study reproduce sexually. They also represent the katoikogenic type of development, which means that oogenesis, fertilization, and embryogenesis take place in the diverticula, which are sac-like outpocketings of the ovariuterine tubules. Formation of a lumen in the diverticulum is indispensable for sperm entry to enable fertilization and subsequent embryogenesis. The aim of the study was to test our hypothesis that the diverticulum lumen forms due to the engagement of the centrally located stalk cells. In this report, we show that in two species of katoikogenic scorpions, at the final stages of oogenesis, the cytoplasm of the stalk cells contains secretory organelles. In the stages preceding fertilization, secretory activity of the stalk cells and fragmentation of their apical parts lead to formation of the diverticulum lumen by a process similar to "cord hollowing" that commonly occurs for lumen formation in other morphogenesis model systems.

Scorpion katoikogenic ovariuterus - Much more alike to apoikogenic type than it seemed to be.

Scorpions are viviparous matrotrophic arthropods. Both, fertilization and embryonic development occur in the female gonad called ovariuterus. Two distinct reproductive patterns are recognized among scorpions: apoikogenic and katoikogenic. In the ovariuterus of apoikogenic scorpions growing oocytes protrude from the ovarian wall and continue previtellogenic and vitellogenic growth on the gonad surface being accompanied by the follicular cells that cover the oocyte surface, and, in most families, the stalk cells that join the oocyte with the ovariuterus wall. In the katoikogenic ovariuterus the oocytes grow in outpocketings of the ovarian wall called diverticula. The aim of our study was to show the development and structure of the diverticula in two katoikogenic scorpions from the family Scorpionidae: Ophistothalmus boehmei and Heterometrus spinifer. We show that the somatic components of each diverticulum develop from the two epithelial layers of the ovariuterine wall. Before fertilization, the wall of the mature diverticula consists of two distinctive epithelial layers: an internal and an external one. Our observations reveal that the epithelial cells of the internal layer of the diverticulum show striking morphological resemblance to the follicular and stalk cells that accompany the growing oocytes in some apoikogenic scorpions. The external epithelial layer of the katoikogenic diverticulum seems to have no equivalents in the apoikogenic type. Functions of the somatic cells of the diverticulum are discussed.

Differentiation of somatic cells in the ovariuteri of the apoikogenic scorpion Euscorpius italicus (Chelicerata, Scorpiones, Euscorpiidae).

In apoikogenic scorpions, growing oocytes protrude from the gonad (ovariuterus) and develop in follicles exposed to the mesosomal (i.e. hemocoelic) cavity. During subsequent stages of oogenesis (previtellogenesis and vitellogenesis), the follicles are connected to the gonad surface by prominent somatic stalks. The aim of our study was to analyze the origin, structure and functioning of somatic cells accompanying protruding oocytes. We show that these cells differentiate into two morphologically distinct subpopulations: the follicular cells and stalk cells. The follicular cells gather on the hemocoelic (i.e. facing the hemocoel) surface of the oocyte, where they constitute a cuboidal epithelium. The arrangement of the follicular cells on the oocyte surface is not uniform; moreover, the actin cytoskeleton of these cells undergoes significant modifications during oocyte growth. During initial stages of the stalk formation the stalk cells elongate and form F-actin rich cytoplasmic processes by which the stalk cells are tightly connected to each other. Additionally, the stalk cells develop microvilli directed towards the growing oocyte. Our findings indicate that the follicular cells covering hemocoelic surfaces of the oocyte and the stalk cells represent two distinct subpopulations of epithelial cells, which differ in morphology, behavior and function.