Blood system responses in inflammation and mechanisms of their development]

A model of acute infectious peritonitis in mice demonstrated that the inflammation is attended by marked biphasic activation of bone-marrow granulomonocytopoiesis and that the activation is due in many respects to increased functional activity of elements forming the hemopoiesis-inducing microenvironment. This was suggested by increased colony-stimulating activity of the marrow mononuclear cells and the content of hemopoietic islets in the marrow. The colony-stimulating activity of peripheral blood also increased. It was established that inflammation is also characterized by activation of bone-marrow erythropoiesis, which is linked with increased erythropoietic activity of the hemopoiesis-inducing microenvironment and blood. There was a relation between the hemopoietic changes and the kinetics of leukocytes in the focus of inflammation.     

Effect of iodine isotope on the pituitary-thyroid and immune systems of children living on the territories polluted by radionuclides

Examination of thyroid function and immune status of children living on the territories polluted by radionuclides in 1993–1994 revealed¹³¹I-dependent thyroid autoimmune reactions. These data indicate a possible effect of¹³¹I on the pituitary-thyroid and immune systems of children living on the radiation controlled territories. Translated fromByulleten' Eksperimental'noi Biologii i Meditsiny, Vol. 126, No. 8, pp. 216–220, August, 1998     

Role of dyslipoproteinemia in the genesis of chronic hepatitis

Laboratory of Experimental Pathomorphology, Research Institute of General Pathology and Pathological Physiology, Russian Academy of Medical Sciences, Moscow. (Presented by Academician of the Russian Academy of Medical Sciences D. S. Sarkisov.) Translated from Byulleten' Éksperimental'noi Biologii i Meditsiny, Vol. 114, No. 10, pp. 437–439, October, 1992.     

Liberation of histamine and serotonin and vascular permeability in an acute aseptic inflammatory focus

Degranulation of mast cells of a peritoneal suspension and of the mesentery of the small intestine and liberation of histamine and serotonin in albino rats with acute aseptic peritonitis were shown to begin during the first minute after injury and to reach a maximum at the fifth minute. By the 15th minute the concentrations of the free amines had fallen sharply and did not differ significantly from the initial levels. The dynamics of the immediate phase of increased vascular permeability corresponded to the dynamics of the free amines. The most marked increase in vascular permeability was observed at the 10th–15th minutes. By the 20th minute it was appreciably lower. Preliminary exhaustion of histamine and serotonin reserves reduced the degree of disturbance of vascular permeability only during the first 15 min after application of the inflammatory agent. It is conculted that histamine and serotonin cause disturbance of vascular permeability in acute aseptic peritonitis chiefly during the first 15 min after injury.Department of Pathological Physiology, Khar'kov Medical Institute. (Presented by Academician of the Academy of Medical Sciences of the USSR A. D. Ado.) Translated from Byulleten' Éksperimental'noi Biologii i Meditsiny, Vol. 84, No. 12, pp. 660–664, December, 1977.     

Mutational analysis of the SOX9 gene in campomelic dysplasia and autosomal sex reversal: lack of genotype/phenotype correlations

It has previously been shown that, in the heterozygous state, mutations in the SOX9 gene cause campomelic dysplasia (CD) and the often associated autosomal XY sex reversal. In 12 CD patients, 10 novel mutations and one recurrent mutation were characterized in one SOX9 allele each, and in one case, no mutation was found. Four missense mutations are all located within the high mobility group (HMG) domain. They either reduce or abolish the DNA-binding ability of the mutant SOX9 proteins. Among the five nonsense and three frameshift mutations identified, two leave the C-terminal transactivation (TA) domain encompassing residues 402-509 of SOX9 partly or almost completely intact. When tested in cell transfection experiments, the recurrent nonsense mutation Y440X, found in two patients who survived for four and more than 9 years, respectively, exhibits some residual transactivation ability. In contrast, a frameshift mutation extending the protein by 70 residues at codon 507, found in a patient who died shortly after birth, showed no transactivation. This is apparently due to instability of the mutant SOX9 protein as demonstrated by Western blotting. Amino acid substitutions and nonsense mutations are found in patients with and without XY sex reversal, indicating that sex reversal in CD is subject to variable penetrance. Finally, none of 18 female patients with XY gonadal dysgenesis (Swyer syndrome) showed an altered SOX9 banding pattern in SSCP assays, providing evidence that SOX9 mutations do not usually result in XY sex reversal without skeletal malformations.