Prenatal development of adenohypophyseal cell types, ovary, and uterus of dromedary camel.

The somatotrophic and thyrotrophic cells were originally developed in the adenohypophysis from undifferentiated chromophobic cells at the foetal age of 4-8 weeks. The follicle-stimulating hormone cells appeared at a foetal age of 24-28 weeks. Prolactin and luteinizing hormone cells were first seen at of foetal age levels of 32-36 and 40 weeks. The germinal epithelium of flattened and cuboidal cells in the ovary was changed to cubical and columnar types, 24-28 weeks of foetal age. The sex cords appeared at 8-12 weeks of foetal age. The primary and secondary follicles were observed at 8-12 and 20-24 weeks of foetal age, respectively. Follicular cavity was noticed at 32-36 weeks, while large follicles encapsulated by follicular sheath were seen in the 40th week of foetal age. Some ovarian follicles degenerated during or after their development. Surface epithelium in the uterus changed from cubical to columnar type at 8-12 weeks of foetal age. The endometrium was clearly distinguished from the myometrium at 16-20 weeks of foetal age. The uterine glands appeared at 16-20 weeks as short and straight tubular glands, and they began to branch in the 40th week of foetal age.

The set of growth factors stimulatory for a transformed rat cell of line NRK-49F depends on the identity of the transforming virus.

Re-cloned rat fibroblast line NRK-49F was transformed by human adenovirus type 5 which had been grown in human cells of the KB carcinoma line. Cell subclones were isolated from seven independent transformation events, and seven untransformed cell subclones were isolated in parallel from control cultures which had been inoculated with lysate of uninfected KB cells. The adenovirus-transformed cells differed from the control untransformed fibroblasts by being typically small and cuboidal, showing multilayered growth, producing colonies in soft-agar medium, and growing to higher saturation density. Adenovirus-transformed subclones showed no infective virus and no consistent difference from control subclones in karyotype (mode = 41). Like the original re-cloned NRK-49F cells, all fourteen subclones required epidermal growth factor, fibronectin, insulin, and retinoic acid for optimal growth in serum-free culture. Thus, transformation by HA5 did not alter the required set, in contrast to the earlier finding that transformation of this same re-cloned line by polyoma virus eliminated the requirements for insulin and retinoic acid.