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Biomedical subjects

T Rogulska

Publications and source records attributed to T Rogulska.

10 recordsLinked to original sources

Migratory mechanisms of chick primordial germ cells toward gonadal anlage.

After appearing at the germinal crescent region, chick primordial germ cells (PGCs) migrate toward the presumptive gonads (pG) till stage 19 (Hamburger and Hamilton, 1951). This study seeks to elucidate the roles of passive and active factors in the PGC-migration, physical trapping of circulating PGCs by the capillary network and PGC attraction by chemotactic factor from presumptive gonads. Firstly, latex beads/pollens (the same size or larger than PGCs) were injected into the embryonic bloodstream at stage 13-19 (when PGCs are in the migrating and settlement phase to the presumptive gonad) in ovo in order to determine whether the PGCs passively reach pG. Most of such particles accumulated in the head region (60%), whereas the remainder did the same in the gonadal region (23% at the peak) at stage 16 when both the head and gonadal regions are rich in capillary plexus. After 3 days, most particles in the gonadal region were located at the angles of dorsal mesentery near the developing gonads where many extra-gonadal PGCs had been located, and a few particles were detected close to the gonad. These results suggest that one of the mechanisms of PGC-migration to the developing gonads is an autonomous trapping of PGCs by the capillary network quite close to the germinal epithelium (GE) and passive translocation by morphogenetic movement. Secondly, the attraction for PGCs by the gonadal anlage proper was examined in ovo using chick and quail embryos. Grafts of quail gonadal anlage containing gonadal epithelium and neighbouring mesenchymal tissue were excised from the quail embryo at stages 12 to 16 (staging by Zacchei, 1961). With the aims of eliminating the influence of surrounding tissue, the quail graft was ectopically transplanted into the posterior to the optic vesicle of 8 to 17 somite chick embryo from the point of a posterior region to the auditory vesicle by a fine tungsten needle under the illumination by the method of Hara (1971). Then the region posterior to the level of presumptive vitelline arteries was surgically excised in ovo. After a 48 hrs.-incubation, the host PGCs which lost their own gonadal anlage as a target organ accumulated in the transplanted quail gonadal anlage originating from the embryo at PGC-migrating periods. This result strongly suggested the presence of some attractive factor that may be emitted from the gonadal anlage proper. Furthermore, it was demonstrated that the PGCs in vitro showed no contact inhibition in relation to other PGCs or fibroblasts in their moving pathway.

Animals↗

[Evaluation of the chorioallantoic membrane in the chick embryo to test the irritation potential of chemical and cosmetic products].

A large number of new chemicals and cosmetics are introduced every year and it is necessary to find a reliable method for the detection of potential irritants. Hitherto used, for this purpose, in vivo rabbit eye test (Draize's test) should be substituted by alternatives because of ethical and legal aspects. One of the most promising method predicting the irritant potential is test performed on the chorioallantoic membrane of the chick embryo (CAM-test) [5]. This membrane is a complete tissue including arteries, capillaries and veins and is technically easy to study. The aim of the study was to check reliability and sensitivity of the test. The principles of the method are simple. The test substance (pure, dissolved or suspended) is applied to the CAM at a volume of 200 microliters. The blood vessels and the remaining parts of the membrane are examined and scored for irritant effects (hyperaemia, lysis or coagulation) after 0.5, 2 and 5 minutes treatment. The numerical, time-dependent score (Table III) are summed to give a single numerical value indicating the irritation potential of the tested substance (Table II). The final assessment is based on the mean value from four experiments. A summary of the results of CAM irritation testing of some of chemicals and cosmetics is given in Tables IV, V and VI. Table VII shows results of assessment of irritation potential of various cosmetics tested by two methods: CAM and Draize eye tests. It was found that CAM test is a rapid and very sensitive method which can give an information on the potential of irritation of chemical substances and cosmetics.

Animal Testing Alternatives↗

Influence of chick or quail embryonic testes on the reproductive system of the quail embryo.

The reproductive system of female quail embryo undergoes masculinization under the influence of chick and quail embryonic testis grafted into an extraembryonic coelom. Müllerian ducts undergo regression. The left gonad transforms into an ovotestis and the right gonad either does not develop or transforms into a small testis. Testicular chick or quail graft does not affect the development of the cortical ovarian-like region in the left testis of male hosts. In some quail testicular grafts developing in female quail hosts cortical region is retained longer than normally.

Animals↗

Influence of embryonic and adult testis on the differentiation of embryonic ovary in the mouse.

The development of 11 1/2-13 1/2-day embryonic mouse ovaries subjected to the influence of adult and embryonic testes was investigated. The environment of adult testis caused severe restriction of ovarian growth, but did not produce any effects which might be considered as masculinization. The presence of embryonic testis was distinctly unfavourable to the embryonic ovary, resulting in restriction of the growth of the latter and degeneration of oocytes. Reversal of the course of differentiation of genetically female germ cells has never been observed.

Animals↗

Meiotic prophase in the left embryonic testis of the Japanese quail (Coturnix coturnix japonica L.).

Spontaneous, transitory feminization of the left embryonic testis occurs in the majority of male Japanese quails from day 11 of incubation until the 2nd day after hatching. The feminized gonad is composed of a testicular part and of an ovarian-like cortical region, which develops outside the tunica albuginea. The cortical region contains numerous germ cells some of which enter meiosis on day 11 (i.e. at the time characteristic of female germ cells) and reach pachytene on day 14. Cortical regions are best developed on day 16 (day of hatching), but regression, accompanied by degeneration of many germ cells, begins shortly afterwards. The mechanism of feminization of the left embryonic testis is discussed.

Animals↗