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Biomedical subjects

S Chakraborty

Publications and source records attributed to S Chakraborty.

At least 145 records · Page 8Linked to original sources

Structural rearrangement of the retinoblastoma gene in human breast carcinoma.

Structural changes of the human retinoblastoma gene have been demonstrated previously in retinoblastoma and some clinically related tumors including osteosarcoma. Structural aberrations of the retinoblastoma locus (RB1) were observed in 25% of breast tumor cell lines studied and 7% of the primary tumors. These changes include homozygous internal deletions and total deletion of RB1; a duplication of an exon was observed in one of the cell lines. In all cases, structural changes either resulted in the absence or truncation of the RB1 transcript. No obvious defect in RB1 was detected by DNA blot analysis in primary tumors or cell lines from Wilms' tumor, cervical carcinoma, or hepatoma. These results further support the concept that the human RB1 gene has pleiotropic effects on specific types of cancer.

Breast Neoplasms↗

Reed-Sternberg cells in Hodgkin's cell lines HDLM, L-428, and KM-H2 are not actively replicating: lack of bromodeoxyuridine uptake by multinuclear cells in culture.

We compared the proliferation of mononuclear and multinuclear cells in four Hodgkin's cell lines, HDLM-1, HDLM-1d, L-428, and KM-H2, by examining their capacity to incorporate bromodeoxyuridine (BrdUrd) into nuclei. Approximately 5% of all cells in HDLM-1 cultures had two or more nuclei, a characteristic of Reed-Sternberg (RS) cells. Unlike mononuclear Hodgkin's (H) cells, these RS cells exhibited no uptake, or only minimal uptake of BrdUrd, suggesting that they did not replicate actively. Cytogenetic study showed that 25% of the HDLM-1 cells contained a tetraploid (4X) set of chromosomes with a characteristic two-peak distribution. Following treatment of HDLM-1 cells with phorbol ester, the percentages of 4X cells and RS cells increased to 50% and 12%, respectively. This increase in RS cells was not likely to be due to cell fusion as shown by the absence of hybridization of BrdUrd-positive and -negative nuclei. Phorbol ester has a short-term effect of blocking the exit of cells from G1 into S phase, but no effect on the transition from S phase to G2/M phase. The block is more prominent in 2X cells than in 4X cells, which may explain the increase in percentage of 4X cells in phorbol ester-treated cultures. In addition, phorbol ester induced the differentiation of H-RS cells, which was accompanied by loss of the marker HeFi-1 from the cell surface. Approximately one third of the RS cells did not express HeFi-1, or expressed only minimal amounts. The findings led us to the following conclusions: (1) The 4X cells probably are formed from 2X H cells as a result of disturbed cytokinesis, but not a cell fusion. (2) A considerable number of 4X cells were H cells, because the number of 4X cells consistently exceeded that of RS cells. (3) Since mitotic figures are extremely rare in RS cells and these cells did not show active BrdUrd uptake, the increased number of RS cells must also be a consequence of disturbed cytokinesis of H cells or a result of nuclear transformation (twisting, convolution, or separation of the nucleus) in H cells. (4) Most RS cells lose their proliferating capacity and some RS cells may undergo further differentiation. Uptake of BrdUrd and phorbol ester induction were also studied on the other three H-RS cell lines, HDLM-1d, L-428, and KM-H2, with results similar to those for HDLM-1.

Biological Transport↗

Influence of some dietary chemopreventive agents on the expression of functional differentiation of the mouse mammary gland in vitro.

The purpose of the present studies was to determine the influence of the chemopreventive agents selenium, 4-(hydroxyphenyl)-retinamide (4-HPR) and beta-carotene, on functional differentiation (lactogenesis) of the mouse mammary gland cells. The hormone-induced expression of the milk-protein genes, beta-casein, epsilon-casein and the whey acidic protein (WAP) was used as molecular marker of differentiation of the mammary cells in organ culture medium containing insulin, prolactin, aldosterone and hydrocortisone. Quantitative determination of the cellular concentration of the respective mRNA was ascertained by molecular hybridization of RNA to the specific cloned cDNA probes using both the solution and the filter hybridization methods. Selenium at 100 nm concentration caused a pronounced inhibition of accumulation of the respective mRNAs. The retinoid, 4-HPR, also caused a dose-dependent inhibition of expression of these mRNA sequences. In contrast, concentrations of the 3 mRNAs in beta-carotene-treated glands remained similar to those observed in glands cultured in medium containing the hormones and hexane (the latter being the solvent for beta-carotene). The significant antagonistic action of selenium and 4-HPR, however, was reversible after removal of the chemicals from the culture medium. Thus, among the 3 chemicals tested, selenium and retinoid can cause an adverse effect on functional differentiation (lactogenesis) of the mammary cells. This inhibitory effect, however, was reversible. beta-Carotene, on the other hand, caused no apparent antagonistic effect on expression of the milk-protein genes in the isolated whole mammary organ in culture.

Actins↗

Hematological changes produced by lindane (gamma-HCH) in six species of birds.

Hematological changes were studied after oral administration of lindane (gamma-hexachlorocyclohexane) at 5 mg/kg body weight twice in 1 week in 6 species of agriculturally important birds: house sparrow, baya weaver bird, common myna, rose-ringed parakeet, blue rock pigeon and domestic duck. Lindane induced anemia in the birds as judged by reduced RBC count, hematocrit and hemoglobin content with corresponding changes in MCV, MCH and MCHC. Bleeding and clotting time were markedly prolonged. Splenic cell counts were decreased with marginal increase of splenic weight in most of the lindane fed birds. Total leucocyte counts were increased while the differential counts of WBC show marked heterophilia and eosinophilia with a decrease in monocyte, lymphocyte and basophil numbers. Domestic duck appears to be somewhat resistant compared to the wild birds studied. Besides anemia the results suggest both immunosuppression and stress effects and indicate that early hematological changes induced by lindane may serve as an initial warning for pesticide toxicity.

Animals↗

Nucleic acids in the spermatozoa of pure and strain crosses of White Leghorn cockerels.

Nucleic acids (DNA and RNA) were estimated in the spermatozoa of three pure strains (M, N and P) and three strain crosses (N X P, M X N and P X M) of White Leghorn cockerels. The average DNA content was 2.31 +/- 0.06 X 10(-9)mg/sperm. Most was found in the P X M strain cross and least in the P strain. The DNA content of the P strain was significantly lower than that in the other strains and it also had the lowest fertility and hatchability of all the strains. The average RNA content in poultry spermatozoa was 0.0522 +/- 0.0038 X 10(-9)mg/sperm. Again, most RNA was found in the P X M strain cross and least in the P strain. The P X M strain cross had a significantly higher RNA content than the rest of the strains. Thus, the P X M strain contained the most DNA and RNA whereas the P strain had least.

Animals↗

Estradiol modulation of pineal gland activity in the wild bandicoot rat, Bandicota bengalensis.

In the present study, the effect of estradiol dipropionate on the cytology and mitotic activity of the pineal gland was evaluated in adult ovariectomized and juvenile bandicoot rats, Bandicota bengalensis. Estradiol treatment for 5 days inhibited the ovariectomy-induced hypertrophy of the pineal gland, and increased the nuclear diameters of pinealocytes in juvenile males while having no effect on the pineal cytology of juvenile females. Estradiol injection induced mitosis in the pinealocytes of adult ovariectomized and juvenile bandicoot rats. Thus, estradiol exhibited a dual action (stimulatory and inhibitory) on the pineal gland of this wild rat.

Animals↗

Density of Culex vishnui and appearance of JE antibody in sentinel chicks and wild birds in relation to Japanese encephalitis cases.

In the District of Burdwan, a rural area of West Bengal State, India, Japanese encephalitis (JE) virus is endemic. In one village a longitudinal survey was conducted in order to find out whether associations could be established between the density of the vector mosquito Culex vishnui in two types of resting places, the incidence of infections in sentinel chicks exposed at monthly intervals, the prevalence of antibodies in wild birds and the occurrence of clinical infections in the human population. The experiment lasted from August 1981 till August 1982. Meteorologically a summer season (March-June), a rainy season (July-October) and a winter season (November-February) are distinguished. In the sentinel chicks infections were observed in all three seasons; in wild birds antibodies were prevalent throughout the year; these observations suggest perennial transmission of the virus in its maintenance cycle. Human infections were observed periodically with, in August 1982, a pronounced peak; this may point to fluctuations in the level of circulation of the virus in its maintenance cycle and spillover to the human population at times of peak circulation. The peaks may be related to the influx of young non-immune birds and newborn mammals into the animal population in summer. Further studies, including virus isolation attempts from mosquitoes and nestling birds, are required to prove this hypothesis.

Animals↗

A generally applicable improved method for preparation of single stranded cDNA probes from clones constructed in M13 vectors.

A generally applicable simplified procedure for the preparation of radiolabeled cDNA hybridization probes from cDNA clones in M13 (M13mp8) bacteriophage vectors is described. A cDNA copy of the insert DNA is synthesized by controlled reaction with the Klenow fragment of E. coli DNA polymerase I, primed with oligo-dT or sequencing primer. The cDNA is separated from the recombinant phage DNA template by alkaline gel electrophoresis. Sensitivity of the cDNAs was tested by quantitative measurement of specific mRNAs in solution hybridization under RNA (R0t analysis) or cDNA (RNA titration) excess conditions. The procedure permits measurement of mRNA levels as small as 0.00001-0.00006% in total RNA preparation. Cellular accumulation of hormone-induced mRNAs for the milk proteins, whey acidic protein and epsilon-casein was also measured using the cDNAs.

Animals↗