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Query: UMLS:C0276640 (TEM)
 20,729 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

The ultimobranchial cysts in the thyroid of the adult guinea pig are identified by a cytochemical method. The ultimobranchial tissue has the shape of an irregular cyst, with non-specific esterase activity that is resistent to HgCl2 inhibition. The TEM reveals five different types of epithelial cell in the cyst wall: 1. cells with deeply invaginated nuclei and of varying shape, from flat to cylindrical but most of them cuboidal. 2. Mucous cells that are tall and similar to goblet cells. 3. Tall cells with big granules that have a dense core. 4. Ciliated cells similar to those in the respiratory tract. 5. C-cells crowded with the small dense granules typical for the cell type. The cyst is enveloped by rather coarse collagen fibers and many wide sinusoids.
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PMID:Fine structure of the ultimobranchial cysts in the thyroid of the adult guinea pig. 92 41

In a leukaemic patient presenting a septicaemia treated with ceftazidime and amikacin, two clinical Escherichia coli isolates distinguished by their level of resistance to oxyimino-beta-lactams were isolated at an interval of 24 h. The isolates were identified by biotyping and esterase electrophoretic typing and the two host strains were shown to be identical. However, each of these strains exhibited a different transferrable extended-spectrum beta-lactamase. These enzymes had different pI values (5.25 and 5.58), but were both blaTEM-1 mutants. The enzyme with pI 5.25 was identical to TEM-101 (TEM-12) (serine 162 substitution). The enzyme with pI 5.58 showed an additional amino acid substitution (lysine residue instead of an arginine at position 237) and was denominated TEM-23. These data indicate that point-mutations can be successively cumulated in vivo by blaTEM mutants, leading to expression of beta-lactamases with increased hydrolysis rates.
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PMID:Two variants of transferrable extended-spectrum TEM-beta-lactamase successively isolated from a clinical Escherichia coli isolate. 150 39

We developed a method for avoiding contamination by fibroblasts when cultures of peritoneal cells are initiated. Macrophages were identified by immunogold detection [light microscope, transmission (TEM) and scanning (SEM) electron microscopes] of membrane antigens (Mac-1+, Thy-1,2-), non-specific esterase activity and ultrastructural features (TEM). As compared with controls, the yield of peritoneal macrophages was 2- and 12-fold higher, respectively, in acutely and chronically infected mice. In all, 30 "chronic", 18 "acute" and 18 control cultures were followed up. At a given cell-density seeding, the decline of control, "acute" and "chronic" cultures starts at about day 10, 15, and 27, respectively. In "chronic" cultures only, fibroblast-like cells appear from day 6 onwards; their number increases with time. Cells showing characters intermediary between macrophages and fibroblasts were observed. We suggest that fibroblast-like cells result from the in vitro transdifferentiation of a limited number of in vivo committed macrophages.
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PMID:Schistosomiasis and in vitro transdifferentiation of murine peritoneal macrophages into fibroblastic cells. 251 39

Cell surface markers, enzymatic patterns, proliferation characteristics and metastatic behaviour of the DSA/2 derived SL2 lymphoma were determined. SL2 cells are sensitive to a heterologous antiserum to murine T-cells and to allo-antisera for Thy 1.2 and TL 1.2.3. They show acid-phosphatase, betaglucuronidase, acid-alpha-naphthytesterase and non-specific esterase staining. The reactions for ATP-ase, and 5'nucleotidase were negative. The SL2 tumour cells can be transplanted in vivo, growing rapidly both as an ascites or a solid tumour, and can be grown in vitro as a suspension culture (doubling time about 18 hours). One hundred cells kill an animal after i.p. transplantation, while 1,000 cells kill an animal after s.c. transplantation. Histopathological examination combined with TEM shows that SL2 metastasizes rapidly, especially after i.p. injection. The metastasizing cells reach the blood vessels in the lung septa and extravascular positions in the liver.
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PMID:Staging, growth properties and metastatic behaviour of a transplantable murine T-cell lymphoma. 612 81

This review is based on the findings of multiparameter studies performed on cells obtained from over 200 cases of leukemia and illustrates the wide range of laboratory tests currently available for cell phenotype identification. Immunological techniques are not discussed and the review deals mainly with light and electron microscopic cytochemistry, transmission (TEM) and scanning electron microscopy (SEM). The importance of light microscopic cytochemistry is clearly demonstrated. In particular, paranuclear acid phosphatase, non-specific esterase (NSE) and diaminopeptidase staining are recommended as reliable T-cell markers. Ultrastructural identification of unclassified leukemic cells using techniques to detect myeloperoxidase, acid phosphatase, platelet peroxide (PPO) and NSE, is shown to be of great importance in cases of early myelo-monoblastic differentiation with negative light microscopic cytochemistry. SEM is also shown to be a reliable means of distinguishing lymphoid and non-lymphoid leukemia when some degree of differentiation is present. However SEM does not appear to contribute in the diagnosis of unclassified leukemia. The new scanning immunoelectron microscopy (SIEM) technique employing heteroantisera or monoclonal antibodies conjugated to latex microspheres (immunolatex) to detect surface receptors and specific antigens is also illustrated. This technique displays the topography of surface antigens on the cell surface of leukemic cells in 3-dimension and facilitates simultaneous visualization of the surface architecture of the labelled cells.
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PMID:Cytochemistry and ultrastructure in lymphoma and leukemia: utility in the diagnosis of different leukemias and the recognition of subtypes of lymphoproliferative disorders. 637 13

Cultures derived from thymus fragments of embryonic (18-19 day old), newborn or one month old C57BL mice have been characterized functionally l(phagocytic and nonspecific esterase activities) and morphologically by means of light, scanning (SEM) and transmission (TEM) electron microscopy. The observations show the heterogeneity of the cell populations composing the monolayers. After a few days incubation macrophages appear as the predominating cell type, while epithelial cells usually constitute no more than 30% of the cells. Experiments designed to determine the fate of lymphocytes adhering to the monolayers lead us to believe (on the basis of SEM morphometric analysis) that the survival of lymphocytes attached either to thymic macrophages or to epithelial cells is improved during the first days of coculture. This survival enhancement does not, however, appear to be a specific inductive effect since a similar survival increase is found when lymphocytes adhere to non-thymic cells. In contrast with the monolayer, the explant provides a three-dimensional culture system able to preserve intact thymic microenvironmental conditions since numerous lymphocytes are found even in five week old cultures which were not overlaid with thymocytes or spleen cells.
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PMID:Thymic microenvironment and cultures derived from mouse thymic explants. A morphological study. 697 Jun 22

Resistance to organophosphates in Culex mosquitoes is typically associated with increased activity of non-specific esterases. The commonest phenotype involves two elevated esterases, A2 and B2, while some strains have elevation of esterase B1 alone. Overexpression of the two B esterase electromorphs is due to gene amplification. Full-length cDNAs coding for amplified esterase B genes from a resistant Cuban strain (MRES, with amplified B1 esterase) and a Sri Lankan strain (PelRR, with amplified B2 esterase) of C. quinquefasciatus have been sequenced. In addition, a partial-length cDNA coding for a B esterase from an insecticide-susceptible Sri Lankan strain (PelSS) has been sequenced. All the nucleotide sequences and the inferred amino acid sequences show a high level of identify (> 95% at the nucleotide and amino acid level), confirming that they are an allelic series. The two B1 esterase nucleotide sequences (MRES and the previously published TEM-R [Mouches, Pauplin, Agarwal, Lemieux, Herzog, Abadon, Beyssat-Arnaouty, Hyrien, De Saint Vincent, Georghiou and Pasteur (1990) Proc. Natl. Acad. Sci. U.S.A. 87, 2574-2578]) showed the lowest identity, and restriction-fragment-length-polymorphism analysis of the two strains was different. On the basis of these data we suggest that the two electrophoretically identical B1 esterase isoenzymes from California and Cuba have been amplified independently. Alternatively, if amplification has occurred only once, the original amplification has not occurred recently.
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PMID:The independent gene amplification of electrophoretically indistinguishable B esterases from the insecticide-resistant mosquito Culex quinquefasciatus. 753 Apr 48

Cisplatin is a potent anti-cancer agent which has been shown to activate Kupffer cells. These activated macrophages demonstrate an increase in extensions, lysosomes, and peroxisomes increasing their anti-tumor activity. Wistar rats were treated with cisplatin (9 mg/kg) and sections of liver were excised for light and electron microscopic analysis at 1, 6, 15, and thirty days post treatment. Non-specific esterase staining was used to differentiate Kupffer cells using light microscopy, morphologic criteria were used for TEM analysis. Liver sections taken 6 days post treatment showed the greatest number of activated macrophages, with the highest degree of activation. Interaction between natural killer cells and Kupffer cells was only seen 6 days post treatment. These results show that cisplatin's ability to enhance the immune system requires several days post treatment to reach maximum potency.
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PMID:Histochemical and morphological identification of Kupffer cells activated by cisplatin. 1036 46

We have investigated the tissue distribution of overproduced esterases A (A1 and A2) and B (B1 and B2) in strains of Culex pipiens L. by immunocytochemistry. S-LAB mosquitoes, lacking overproduced esterases, were used as reference. Tissues showing a strong specific reaction (fluorescence) were observed with anti-esterase A1 antiserum in S54 (with A1) and BOUAKE (with A2) strains, and with anti-esterase B1 antiserum in TEM-R and EDIT (with B1) and BOUAKE (with B2) strains. Overproduction of esterases A and B was tissue-specific. The most constant pattern for the two types of esterases was their overproduction in the alimentary canal and Malpighian tubes, although fluorescence varied in intensity depending on strains and developmental stages. There was no difference in the tissue distribution of esterases Al and A2. In contrast, esterases B pattern was highly variable among strains. Differences between TEM-R and EDIT were explained by the different overall overproduction and number of copies of the amplified gene (10-fold higher in TEM-R). The most striking difference in esterase B1 and B2 tissue localization concerned the nervous system where neurons were intenisely fluorescent in TEM-R and EDIT (B1), but not in BOUAKE (B2). All esterase B positive tissues in TEM-R contained large quantities of esterase B1 mRNA (in situ hybridization), indicating that at least part of the protein revealed by immunochemistry was produced in the tissues where it was observed. Our results are discussed in terms of the protection that the different esterases can confer during exposition to organophosphorous insecticides.
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PMID:Tissue localization of overproduced esterases in the mosquito Culex pipiens (Diptera: Culicidae). 1176 76

The fine structure of the epithelium lining the tympanic cavity of the chicken was studied by TEM and SEM. In addition, the distribution of nonspecific esterase activity in the epithelium was investigated by TEM. Ultrastructural study revealed the presence of disk-like apical protrusions of the epithelial cells, previously not observed in other cell types. The protrusions contained some cytoplasmic organelles and were characterized by a ring-shaped thickening around their periphery. The ring was made up of a granulo-filamentous material. Our observations clearly indicate the existence of an apocrine secretory mechanism, consisting of a progressive detachment of disk-like protrusions from the apex of the epithelial cells. The ultracytochemical study demonstrated nonspecific esterase activity on the epithelial surface and in the secretory vesicles. We propose that nonspecific esterase is a marker for middle ear surfactant in birds.
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PMID:Ultrastructural and ultracytochemical study of the middle ear epithelium in the chicken, Gallus gallus domesticus. 1265 18


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