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J Crocker

Publications and source records attributed to J Crocker.

214 records · Page 12Linked to original sources

The enzyme histochemistry of lymphoid and non-lymphoid cells of the human palatine tonsil: a basis for the study of lymphomas.

The distribution of various hydrolytic enzymes has been determined in 27 human palatine tonsils by means of conventional enzyme histochemical techniques, and lysozyme (muramidase) activity has been localised in eight tonsils by the unlabelled antibody peroxidase-antiperoxidase complex (PAP) method. The enzyme activities of various cell types are compared and the effect of various methods of fixation and processing discussed. The results suggest that arrangement of various histiocytic cells types within the tonsillar follicles and crypt epithelium is related to the processing of antigen. The PAP method for lysozyme demonstrates a smaller population of cells than is demonstrated by the alpha-naphthyl acetate esterase (ANAE) method. T-cells are demonstrated by the presence of dot-like ANAE activity in their cytoplasm. Large numbers of the lymphocytes of this type were located in the T-dependent areas of the tonsil, and are frequent beneath the crypt epithelium. The efferent lymphatic vessels appeared to contain an almost pure population of T-cells. The immunohistochemical method for lysozyme did not differentiate between T- and B-cell areas, dot-like activity being absent. As in other workers' studies on non-lymphoid cells of the murine spleen, several types of glass-adherent cells have been identified in short-term cell cultures from the human tonsil. True dendritic cells and branching macrophages differ in several ways (as in the mouse spleen). The tonsil is considered to be a useful control "reactive" lymphoid organ, to act as a baseline tissue in an extended study of morphology and enzyme histochemistry in the lymphomas.

Adolescent↗

The lining of branchial cysts studied by electron microscopy and enzyme histochemistry.

The lining of five branchial cysts from patients aged from 17 to 51 was studied by histochemical methods for non-specific acid esterase and acid phosphatase and by scanning and transmission electron microscopy. The stratified squamous epithelium was shown to be a specialised structure, with a few microvillous cells on the surface and an intra-epithelial network of channels containing lymphocytes, notable T cells, and mononuclear phagocytic cells. The appearance of the cyst lining was similar to that of the epithelium lining the crypts of palatine tonsils. The demonstration of a complex lympho-epithelial lining of the cysts does not settle the controversial question of their origin, but it must be taken into account by hypotheses explaining the development of branchial cysts.

Adult↗

Quantitative study of the immunoglobulin-containing cells in trephine samples of bone marrow.

Immunoglobulin (Ig) was demonstrated in paraffin sections of 12 trephine bone marrow biopsies by means of the unlabelled antibody peroxidase-antiperoxidase (PAP) method. The Ig-containing cells, which were counted with the Reichert-Jung (Kontron) MOP-AMO(3) user-controlled image-analyser, were found to constitute approximately 4.2% of all the nucleated cells in the marrow, a figure significantly higher than those reported by previous workers.

Bone Marrow↗

A study of nuclear diameters in lymph node imprints using the Zeiss Microvideomat.

The diameters of the cell nuclei were measured in imprint preparations of eight tonsils and 28 lymph nodes, each specimen being from a separate patient. The lymph nodes were from cases of Hodgkin's disease (HD), non-Hodgkin's lymphoma (NHL), and reactive benign states. The nuclear diameters were measured by means of an image-analysing device, the Zeiss Microvideomat. For accurate measurements, the cells had to be well separated, and tissue sections could not be used because the close juxtaposition of nuclei gave erroneous readings. However, cell imprints proved suitable. The results show that the mean nuclear diameters for the HD, NHL, and reactive groups differ and show a considerable scatter. However, the distributions for the NHL and reactive nodes are sufficiently different to suggest that the method may have diagnostic value for the former.

Adolescent↗

An immunohistochemical and clinicopathological study of granulocytic sarcoma ('chloroma').

A small series of granulocytic sarcomas (GS) or 'chloromas' has been studied by means of conventional histology and immunohistochemistry. The latter was found to be most useful in the diagnosis and characterization of these neoplasms, which are rare in Great Britain. Polytypic antisera to leukocyte elastase and cathepsin G have proved to be most useful, giving intense staining in all cases. These two markers are more specific than muramidase (lysozyme) and alpha 1-antitrypsin, since, unlike the latter two, they do not stain histiocytic cells. The results of staining with two monoclonal antisera, AGF 4.48 and AGF 4.36, are also described. In addition, the clinicopathological details of the seven cases are summarized and the literature is briefly surveyed.

Adult↗

Differences in adiponectin protein expression: effect of fat depots and type 2 diabetic status.

Adiponectin is an adipocyte-derived hormone associated with insulin sensitivity and atherosclerotic risk. As central rather than gluteofemoral fat is known to increase the risk of type 2 diabetes and cardiovascular disease, we investigated the mRNA and protein expression of adiponectin in human adipose tissue depots. RNA was extracted from 46 human adipose tissue samples from non-diabetic subjects aged 44.33 +/- 12.4 with a BMI of 28.3 +/- 6.0 (mean +/- SD). The samples were as follows: 21 abdominal subcutaneous, 13 omentum, 6 thigh; samples were also taken from diabetic subjects aged 66.6 +/- 7.5 with BMI 28.9 +/- 3.17; samples were: 6 abdominal subcutaneous; 3 thigh. Quantitative PCR and Western analysis was used to determine adiponectin content. Protein content studies determined that when compared with non-diabetic abdominal subcutaneous adipose tissue (Abd Sc AT) (values expressed as percentage relative to Abd Sc AT -100 %). Adiponectin protein content was significantly lower in non-diabetic omental AT (25 +/- 1.6 %; p < 0.0001, n = 6) and in Abd Sc AT from diabetic subjects (36 +/- 1.5 %; p < 0.0001, n = 4). In contrast, gluteal fat maintained high adiponectin protein content from non-diabetic patients compared with diabetic patients. An increase in BMI was associated with lower adiponectin protein content in obese ND Abd Sc AT (25 +/- 0.4 %; p < 0.0001). These findings were in agreement with the mRNA expression data. In summary, this study indicates that adiponectin protein content in non-diabetic subjects remains high in abdominal subcutaneous fat, including gluteal fat, explaining the high serum adiponectin levels in these subjects. Omental fat, however, expresses little adiponectin. Furthermore, abdominal and gluteal subcutaneous fat appears to express significantly less adiponectin once diabetic status is reached. In conclusion, the adipose tissue depot-specific expression of adiponectin may influence the pattern of serum adiponectin concentrations and subsequent disease risk.

Adipocytes↗

Pleural fluid cytology in lymphoplasmacytoid lymphoma with numerous intracytoplasmic immunoglobulin inclusions. A case report with immunocytochemistry.

Description is given of the cytology and immunocytochemistry of pleural fluid in a case of lymphoplasmacytoid lymphoma with unusually numerous IgM kappa intracytoplasmic inclusions. The therapeutic and prognostic importance of the distinction between this rare vacuolated cell form of lymphoma and metastatic adenocarcinoma is stressed, and the most helpful diagnostic features are discussed.

Aged↗