Frequency and phase correlations of the biorhythms of metabolic indices in mice during their postnatal ontogeny

In laboratory mice the daily rhythms of feeding, plasma insulin, blood glucose and liver glycogen were investigated beginning from an age of 1 week to 52 weeks. For all parameters circadian and ultradian rhythms changing in the course of development could be quantified. During juvenile phase and inversion of all patterns connected with temporary increasing ultradian components takes place. The beginning and the end of this inversion are specific for various parameters, to that changing frequency and phase correlations could be obtained. The lowest degree of phase correspondence is found at weaning, it reaches its maximum in adults and decreases again in older mice. The possible consequences of demonstrated phenomena for the stability of the functional system and the existence of sensitive phases during postnatal ontogeny are discussed.     

Dynamic aspects of trypsin-giemsa banding.

The trypsin-Giemsa banding procedure was adapted so that chromosomes could be observed through the microscope during treatment and staining. Trypsin treatment resulted only in a swelling of the chromatids. Chromosome bands which appear as raised structures with interference contrast optics emerged only after staining with Giemsa. These structures remain after Giemsa destaining, suggesting that an irreversable change in chromosome structure is induced by Giemsa. Observations of the stain flow indicate that the positioning of the chromosomes has an effect on the quality of band production. These studies also revealed that bands appear in a reproducible sequence on individual chromosomes, which suggests that alterations take place at different rates along the length of the chromosomes.     

Impaired melanoma growth in VASP deficient mice

Progression of tumors depends on interactions of cancer cells with the host environment. Expression of the cytoskeleton protein VASP is upregulated in various cancer entities. We analyzed the role of VASP for melanoma growth in murine allograft models. Growth of VASP expressing melanomas was retarded in VASP^?/? versus wild-type animals. Over time tumor size was <50% in VASP^?/? versus wild-type animals and independent of expression levels of Ena/VASP protein family members. Histological analyses showed smaller cells with impaired nutrition status and less vascularization in melanomas derived from VASP^?/? versus counterparts from wild-type mice. Cumulatively, the data reveal a critical role of VASP in non-tumor cells in the tumor environment for melanoma growth in vivo.