Microfluorometry and image analysis of peritoneal mast cells reveal differences in the morphology and content of sulfated polyanions between normal and tumor-bearing mice

Mast cells (MC) are frequently increased in neoplasias. Recently, we observed that MC from peritoneal cavity of normal mice (NMC) and one of their mediators (heparin) decreased M3 tumor incidence and tumor cell proliferation in vitro, while MC from peritoneal cavity of tumor-bearing mice (TMC) had n...

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Autor principal: Bertolesi, G.E
Otros Autores: Stockert, J.C, De Cidre, L.L
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: 1997
Acceso en línea:Registro en Scopus
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100 1 |a Bertolesi, G.E. 
245 1 0 |a Microfluorometry and image analysis of peritoneal mast cells reveal differences in the morphology and content of sulfated polyanions between normal and tumor-bearing mice 
260 |c 1997 
270 1 0 |m Bertolesi, G.E.; Catedra de Histol. Animal (Lab 26), Departamento de Biologia, Facultad Ciencias Exactas Naturales, Buenos Aires 1428, Argentina 
506 |2 openaire  |e Política editorial 
504 |a Metcalfe, D.D., Mast cell mediators with emphasis on intestinal mast cells (1984) Allergy, 53, pp. 563-575 
504 |a Schwartz, L.B., Austen, K.F., Structure and function of the chemical mediators of mast cells (1984) Prog Allergy, 34, pp. 271-321 
504 |a Langer, J., Liebman, S., Monk, P.K., Pelletir, G.S., Mast cell mediators and peritoneal adhesion formation in the rats (1995) J Surg Res, 59, pp. 244-348 
504 |a Dabbous, M., Walker, R., Haney, L., Carter, L.M., Nicolson, G.L., Woolley, D.E., Mast cells and matrix degradation at sites of tumor invasion on rat mammary adenocarcinoma (1986) Br J Cancer, 54, pp. 459-464 
504 |a Roche, W., The nature and significance of tumor associated mast cells (1986) J Pathol, 148, pp. 175-182 
504 |a Rosengard, B.R., Mahalike, Cochrane, D., Mast cell secretion: Differences between immunologic and non immunologic stimulation (1986) Agents Actions, 19, pp. 3-4 
520 3 |a Mast cells (MC) are frequently increased in neoplasias. Recently, we observed that MC from peritoneal cavity of normal mice (NMC) and one of their mediators (heparin) decreased M3 tumor incidence and tumor cell proliferation in vitro, while MC from peritoneal cavity of tumor-bearing mice (TMC) had no effect. The purpose of this study was to evaluate the differences in morphology and content of sulfated glycosaminoglycans between NMC and TMC. Both were stained with Mayer's haematoxylin-Rubipy [tris (2,2'-bipyridine) ruthenium (II)] sequence, a specific technique to detect sulfated polysaccharides. Image processing and analysis (IPA) confirmed densitometric and microfluorometric studies and revealed several structural characteristics of MC. TMC were partially degranulated with smaller surface and greater perimeter than NMC. Shape factor, which reflects the sphericity grade of the cell (1 = spherical), was three-fold increased in TMC in relation to NMC (6.15 vs 1.76, respectively). Also, TMC had less than a half sulfated polysaccharides compared to NMC. We conclude that subcutaneous tumor grafts mediate degranulation of MC from peritoneal cavity with the consequent release of MC mediators such as heparin. This may be one of the factors for the absence of antitumoral effect of TMC.  |l eng 
593 |a Department of Biology, Fac. of Exact and Natural Sciences, University of Buenos Aires, Argentina 
593 |a Department of Biology, Faculty of Sciences, Autonomous University of Madrid, Spain 
593 |a Cátedra de Histol. Animal, Departamento de Biología, Ciudad Universitataria, Buenos Aires 1428, Argentina 
690 1 0 |a ADENOCARCINOMA 
690 1 0 |a HEPARIN 
690 1 0 |a IMAGE ANALYSIS 
690 1 0 |a MAST CELL 
690 1 0 |a TRIS (2,2'-BIPYRIDINE) RUTHENIUM (II) 
690 1 0 |a ADENOCARCINOMA 
690 1 0 |a ANIMAL CELL 
690 1 0 |a ARTICLE 
690 1 0 |a BREAST CARCINOMA 
690 1 0 |a IMAGE ANALYSIS 
690 1 0 |a MAST CELL DEGRANULATION 
690 1 0 |a MICROFLUOROMETRY 
690 1 0 |a MOUSE 
690 1 0 |a NONHUMAN 
690 1 0 |a PERITONEUM MAST CELL 
690 1 0 |a PRIORITY JOURNAL 
690 1 0 |a TUMOR GROWTH 
700 1 |a Stockert, J.C. 
700 1 |a De Cidre, L.L. 
773 0 |d 1997  |g v. 11  |h pp. 1221-1225  |k n. 6  |p INT. J. ONCOL.  |x 10196439  |t International Journal of Oncology 
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