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PubMed1963

A histochemical study of phagocytic and enzymatic functions of rabbit mononuclear and polymorphonuclear exudate cells and alveolar macrophages. I. Survey and quantitation of enzymes, and states of cellular activation.

The cytochrome oxidase (CO), aminopeptidase (AMP), succinic dehydrogenase (SD), acid phosphatase, esterase, and alkaline phosphatase of rabbit mononuclear (MN) and polymorphonuclear (PMN) peritoneal exudate cells and pulmonary alveolar macrophages (AM) - air dried on Mylar strips - were characterized by histochemical techniques with respect to stability, activators, inhibitors, and pH optima. A granule count method was established for the quantitation of these enzymes. For the acid phosphatase of MN, in which the most precise results were obtained, time, pH, substrate, and inhibitor curves resembled those commonly obtained biochemically. Five of these enzymes were usually more active in AM than MN, whereas the sixth, alkaline phosphatase, was not present in either cell type. AM also tended to consume more oxygen than MN and to divide more frequently. Since the most active cells in the population would be first involved in the host's defense against microbial agents, a comparison was made of the 10 per cent of the AM and MN with the highest enzymatic activities. No differences were found in the granule counts that were not reflected by the means. However, within a given AM population, cells containing ingested dust particles seemed to have higher enzymatic activities than those without particles. MN had greater acid phosphatase and SD activities than PMN and consumed more oxygen, but the CO, AMP, and esterase activites of both types of cells were of similar magnitude. PMN showed high alkaline phosphatase activity; MN showed none. A survey of the histochemical literature indicates that a positive correlation between the enzymatic and phagocytic activities of both MN and PMN exists in vivo.

Acid Phosphatase↗
PubMed1963

EFFECTS OF MALIGNANT EFFUSIONS ON THE MITOTIC INDEX OF L STRAIN MOUSE CELLS GROWN IN TISSUE CULTURE.

By employing a clone of L strain mouse fibroblasts (L(E)) which does not exhibit cell clumping and lysis (cytolytic antibody reaction), it was possible to screen for the presence of growth-regulating factors in human sera and effusions, exclusive of an antigen-antibody reaction. Under conditions of the test a mitotic index greater than 20% indicated the presence of a growth-promoting factor.A total of 11 pleural effusions was tested. Four of the eight malignant effusions possessed a growth-promoting factor, while none of the three non-malignant effusions or the one sample of human umbilical cord serum possessed such a factor. Overnight storage of the unfiltered effusions at 5 degrees C. resulted in complete loss of the growthpromoting activity.

Animals↗
PubMed1964

DETECTION OF PERICARDIAL EFFUSION BY RADIOISOTOPE HEART SCANNING.

A marked difference between the cardiac silhouette on the six-foot chest roentgenogram and the cardiac blood pool, determined by radioisotope scanning, has been shown to be consistent with pericardial effusion and/or thickening. It has also been observed that the cardiac blood pool is separated from the liver margin by the interposition of pericardial fluid and/or thickening. This separation was not demonstrated in the presence of a normal pericardium. To appreciate these features, 400 muc. of radioiodinated human serum albumin and 50 muc. of colloidal radiogold were used for scanning. The former outlind the blood pool and the latter demonstrated the position of the liver.

Exudates and Transudates↗