Film Reviews

Vision of Juazeiro . 1970. Directed by Eduardo Escorel
Chichicastenango . 1987. A video by Claudia Feldmar
Comalapa: Traditions and Textures . 1987. A video by Claudia Feldmar
Holy Week in Antigua, Guatemala . 1987. A video by Claudia Feldmar
Sacred Games: Ritual Warfare in a Maya Village . 1988. A film by Thor Anderson
Peru—When the World Turned Dark . 1988. Produced by Maria Luisa Lobo and directed by Gianfranco Annichini     

Defenses against oxidative stress in the Antarctic scallop Adamussium colbecki and effects of acute exposure to metals

Since a general pathway of toxicity induced bypollutants is the enhancement of reactive oxygenspecies, biochemical responses associated withvariations in the antioxidant cellular system havebeen often proposed as biomarkers ofpollutant-mediated toxicity associated with oxidativestress. Antarctic organisms live in an extremeenvironment characterized by low water temperature,high level of dissolved oxygen, presence of ice andstrong seasonal changes in light intensity andavailability of food, conditions which could influenceboth the formation of reactive oxygen species and themechanisms for their removal. In this respect andconsidering the utility of this as a key species formonitoring marine Antarctic environment it was ofinterest to investigate the antioxidant defense systemof the scallop Adamussium colbecki.The parameters examined in the digestive gland of thescallop were the concentration of glutathione and theactivity of several glutathione dependent andantioxidant enzymes (glyoxalase I and II, glutathioneS-transferases, glutathione peroxidases, glutathionereductase, catalase, superoxide dismutase). Very highlevels of catalase suggest a possible adaptation toAntarctic extreme conditions, while the highactivities of glutathione S-transferases are moreprobably related to the feeding behavior of Pectinids.Enzymes from Adamussium colbecki generallyappeared to be active at low temperatures but, with afew exceptions, their activities increased with risingtemperature. Exposure of A. colbecki tosublethal concentrations of Cu or Hg resulted in asignificant reduction in the levels of totalglutathione and in the activity of catalase andglutathione S-transferases. Antioxidant responses ofA. colbecki could represent a useful tool inassessing the biological impact of environmentalpollutants in the Antarctic ecosystems.     

Purification and characterization of a protein inhibitor of calcium-dependent proteases from rat liver

Soluble extracts of rat liver contain a protein inhibitor of calcium-dependent proteases. The inhibitor has an apparent M_r = 250,000 and is separated from the calcium-dependent proteases by gel-filtration chromatography in the presence of EGTA. The inhibitor has been purified by affinity chromatography using a calcium-dependent protease covalently linked to Affi-Gel 15. The inhibitor specifically binds to this affinity resin in a calcium-dependent manner and elutes in the presence of EDTA or EGTA. The purified inhibitor appears as a single protein with M_r = 125,000 on sodium dodecyl sulfate-polyacrylamide gel electrophoresis. Presumably it is a dimer under nondenaturing conditions. The inhibitor inhibits each of two calcium-dependent proteases from rat liver and from other tissues and species. However, it has no effect on any other protease tested.     

Immunoglobulin classes of human serum antibodies in vaginal candidiasis

The titre and immunoglobulin class of antibodies against Candida albicans in serum from 60 non-pregnant women was determined. IgG titres up to 132, IgA titres up to 18, and IgM titres up to 14 were detected in 30 women with vaginal candidiasis. Similar titres were found in 20 women harbouring yeasts in the mouth or rectum, and in 10 women who were not harbouring yeasts in the vagina, mouth or rectum. Serum fractionation confirmed that antibodies to C. albicans are found in the three immunoglobulin classes and that these antibodies reside in highest titre in the IgG class. No secretory IgA antibodies against C. albicans were detected in the serum of these women.     

Immunospecificity of nuclear antigens in chicken erythroid cells

Summary Specific antisera were produced against chicken reticulocyte dehistonized chromatin. The antisera reacts strongly with chicken reticulocyte chromatin, but only marginally with chicken erythrocyte chromatin. There is no reticulocyte antigen detected in chicken liver. Reticulocyte maturation is accompanied by a gradual decrease in the chromatin immunological activity and template capacity. The reduction of immunological activity is due to the change of chromatin conformation during erythrocyte maturation. Dehistonization and sonication of erythrocyte chromatin raises the erythrocyte chromatin immunological activity to levels similar to those of reticulocyte chromatin. The erythrocyte nuclear antigens are class specific, not being found in frog erythroid cell or murine Friend leukemia cell chromatins.     

Maintenance and induction of morphological differentiation in dissociated mammary epithelium on floating collagen membranes

Summary Dissociated normal mammary epithelial cells from prelactating mice were plated on different substrates in various medium-serum-hormone combinations to find conditions that would permit maintenance of morphological differentiation. Cells cultured on floating collagen membranes in medium containing insulin, hydrocortisone and prolactin maintain differentiation through 1 month in culture. The surface cells form a continuous epithelial pavement. Some epithelial cells below the surface layer rearrange themselves to form alveolus-like structures. Cells at both sites display surface polarization; microvilli and tight junctions are present at their medium-facing or luminal surface and a basal lamina separates the epithelial components from the gel and stromal cells. Occasinal myoepithelial cells, characterized by myofilaments and plasmalemmal vesicles, are identified at the basal surface of the secretory epithelium. In contrast, cells cultured on plastic, glass or collagen gels attached to Petri dishes form a confluent epithelial sheet showing surface polarization, but lose secretory and myoepithelial specializations. If these dedifferentiated cells are subsequently maintained on floating collagen membranes, they redifferentiate. There is little DNA synthesis in cells on collagen gels, in contrast to Petri-dish controls. Protein synthesis in cells on floating collagen membranes increases over T₀ values and remains constant through 7 days in culture whereas it decreases on attached gels; however, if the gels are freed to float, protein synthesis increases sharply and parallels that seen on floating membranes. The work was supported by USPHS Grants CA-05388 and CA-05045 from the National Cancer Institute, DHEW.     

Insulin-like growth factors, IGF-1, IGF-2 and somatomedin C trigger cell proliferation in mammalian epithelial cells cultured in a serum-free medium

A single insulin-like growth factor which constitutes part of a defined serum-free medium is sufficient to stimulate DNA synthesis and mitosis in mammalian lens epithelial cells. Rabbit lenses were cultured in KEI-4, a medium which mimics rabbit aqueous humor, or in KEI-4 containing insulin growth factor I (IGF I), insulin growth factor II (IGF II) or somatomedin C. The magnitude of DNA synthesis and mitosis was evaluated on whole mount preparations of the epithelium at various times of culture. IGF I and II, the most highly purified of the insulin-like growth factors, and somatomedin C were equipotent lens mitogens, were active at the ng level, were more mitogenic toward lens epithelial cells than insulin, and initiated cell proliferation throughout the normally amitotic central region of the lens epithelium. The time course of the mitotic response elicited by the insulin-like growth factors was identical to that noted in lenses cultured in medium supplemented with serum or insulin. The present results, coupled with those of other investigators, suggest that insulin-like factors may regulate cell division in the mammalian lens in vivo.