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V Bila

Publications and source records attributed to V Bila.

4 recordsLinked to original sources

The role of cell death in limb development of rats manifesting Lx allele on different genetic backgrounds.

Control of vertebrate digital pattern is a phylogenetically old mechanism. Animal strains with abnormal digital counts are a useful model system to study tissue, cell and molecular factors involved in limb patterning. The aim of this study was to investigate rat limb morphogenesis on gestation days 13 to 16 in normodactylous, polydactylous and oligodactylous fetuses where the deviation from the normal pentadactylous phenotype is caused by interaction of mutant Lx allele with different genetic backgrounds. General development was assessed by measurements of crown-rump length, and limb morphogenesis by hand and foot plate width. Skeletogenesis was studied histologically and by whole mount staining with Alcian Blue and Acridine Orange. Cell death was demonstrated by supravital staining and fluorescence microscopy and by standard histology on serial sections. No phenotypic differences among the groups were noted on day 13. On day 14, the oligodactylous hind limb buds were more spiky than normal and had well-developed preaxial necrotic site (foyer preaxial primaire) which was normally observed only on day 15. This area of programmed cell death was severely attenuated in polydactylous limb buds. Pollex triphalangy manifested as increased hand plate width from day 15. Also hind limb buds width differed by this stage between groups. No acceleration or retardation of skeletogenesis was observed in abnormal limbs. The data confirm the crucial role of spatial and temporal patterns of morphogenetic programmed cell death in control of digital pattern.

Alleles↗

Mapping of quantitative trait loci for blood pressure and cardiac mass in the rat by genome scanning of recombinant inbred strains.

In the HXB and BXH recombinant inbred strains derived from the spontaneously hypertensive rat and the normotensive Brown Norway rat, we determined the strain distribution patterns of 500 genetic markers to scan the rodent genome for quantitative trait loci regulating cardiac mass and blood pressure. The markers spanned approximately 1,139 cM of the genome and were tested for correlations with left ventricular mass adjusted for body weight, and with systolic, diastolic, and mean arterial pressures. The marker for the dopamine 1A receptor (Drd1a) on chromosome 17 showed the strongest correlation with left ventricular heart weight (P = .00038, r = -0.59) and the relationship to heart weight was independent of blood pressure. The markers showing the strongest correlations with systolic, diastolic, and mean arterial pressure were D19Mit7 on chromosome 19 (P = .0012, r = .55), D2N35 on chromosome 2 (P = .0008, r = .56), and Il6 on chromosome 4 (P = .0018, r = .53), respectively. These studies demonstrate that the HXB and BXH strains can be effectively used for genome scanning studies of complex traits and have revealed several chromosome regions that may be involved in the genetic control of blood pressure and cardiac mass in the rat.

Animals↗