An immunocytochemical method for quantification of lung tissue fibronectin

A technique to quantify tissue fibronectin was developed, using peroxidase-antiperoxidase immunocytochemistry and automated scanning light microscopy. This technique was developed using isolated perfused rat lungs, some of which were subjected to acute oxidant lung injury. Both injured and control lungs were perfused with solutions containing heterologous fibronectin. The technique clearly demonstrated differences in the amount of tissue fibronectin in injured and noninjured lung as well as differences between lungs exposed to fibronectin and those not exposed. The described technique offers a reliable method for quantifying tissue fibronectin and is sensitive enough to detect differences in tissue fibronectin under experimental conditions of acute lung injury.     

Natural antibody to a human bladder carcinoma cell line

Summary Sera from 144 healthy blood donors were screened for the presence of antibody against the bladder carcinoma cell line RT4 by means of an immune adherence assay. Only one serum (9241) demonstrated high activity with a titer of 1/124. Qualitative and quantitative absorption analyses were carried out with a wide variety of cells to characterize the specificity of the reaction. Cells used for absorption were both cultured and non-cultured and normal and malignant. The reactivity was absorbed by the bladder cancer cell lines RT4 and 5637 and the lung cancer cell line SK-LC-LL. In addition, surgically obtained urothelium from a patient with transitional cell carcinoma abrogated reactivity. No other absorbing cells removed the reactivity of serum 9241 for RT4. The antigen defined by this serologic reaction is heat-stable and trypsin-resistant, as demonstrated by using heated or trypsinized RT4 cells for absorption.This study shows that naturally occurring antibody directed toward cell surface antigens of tumor cells is present in some normal individuals. This finding is important in the evaluation of a possible causal relationship between the presence of antibody specific for tumor cell antigens and the development of neoplasia.     

Logistic growth curve of chickens: heritability of parameters

Parameters of the logistic function of growth, fit to individual body weight curves of two randombred control populations of each sex of chickens from hatching to 45 weeks of age, were evaluated. Growth-rate constant and age at the infection point in the curve were estimated by the method of sample quantiles from individual weekly body weights of 225 males and 281 females of the Rhode Island Red (RIR) line, and 164 males and 239 females of the White Leghorn (WL) line. Heritability estimates, based on correlation among full-sibs, of growth rate constant were 0.18 +/- 0.32 in males and 0.29 +/- 0.29 in females of the RIR line, and 0.41 +/- 0.40 in males and 0.46 +/- 0.32 in females of the WL line. Estimates of heritability of age at the inflection point were 0.36 +/- 0.44 in males and 0.42 +/- 0.32 in females of the RIR line, and 0.46 +/- 0.41 in males and 0.50 +/- 0.28 in females of the WL line. Observed variation for each trait probably does not provide evidence for heritable differences. No genetic correlations were evident among growth-rate constant, age at the point of inflection, and initial or maximum weight. According to these results, it does not appear that selection for growth-rate constant or age at the point of inflection will change the shape of the growth curve of these populations genetically. Moreover, correlated genetic change in initial or maximum weight would not be expected.     

Microanalytical determination of the activities of phospholipases A, C, and D and of their mixtures

In the course of studies on the catabolite repression of succinate dehydrogenase in yeast (1), the need arose to monitor simultaneously phospholipases A and D activities in broken cell preparations. Although a variety of assay methods are described in the literature for both of these enzymes, none of them appeared to provide a simple and unambiguous measure of both activities simultaneously at the very low enzyme concentrations and with the crude enzyme preparations used. Therefore, a method was developed, based on the use of uniformly labeled ¹⁴C-lecithin, which provides simple and relatively easy assays for phospholipases A, C, and D, as well as for mixtures of the three enzymes, and permits initial-rate measurements. Details are described in this paper. Comparison of the methods described with other assays for phospholipases is presented in the Discussion.