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001-es BibID:	BIBFORM068948
Első szerző:	Antal-Szalmás Péter (laboratóriumi szakorvos)
Cím:	Diverging Pathways for Lipopolysaccharide and CD14 in Human Monocytes / Peter Antal-Szalmas, Miriam J. J. G. Poppelier, Roel Broekhuizen, Jan Verhoef, Jos A. G. van Strijp, Kok P. M. van Kessel
Dátum:	2000
ISSN:	0196-4763
Megjegyzések:	Background: CD14 is considered to be the major endotoxin(lipopolysaccharide [LPS]) binding molecule on humanmonocytes. It initiates cellular response, but its rolein the clearance of LPS is not well understood. Underconditions that ensure totally CD14-dependent LPS bindingon human monocytes, the internalization mechanismsof LPS and CD14 were studied.Methods: The uptake and intracellular distribution offluorescein isothiocyanate (FITC)-LPS and CD14 was determinedby flow cytometry, trypan blue quenching, andconfocal fluorescence microscopy. Incubation of surfacebiotinylatedcells with LPS at 37?C or 4?C and subsequentsubfractionation was used to further characterize CD14internalization. The amount of the intracellular CD14 wasestimated by CD14 enzyme-linked immunosorbent assay(ELISA).Results: The internalization rate of 10 ng/ml FITC-LPSwith 1% human serum was 1% of bound endotoxin perminute, whereas CD14 expression did not decrease at thesame time surface. We proved the presence of an intracellularCD14 pool (2.68 3 106 molecules per unstimulatedmonocyte) and could show that internalized FITCLPSmolecules can be found in different intracellularcompartments than CD14. Subfractionation of LPS-treatedbiotinylated monocytes showed no change in biotinylatedCD14 in the membrane fraction independently of theincubation temperature (37?C or at 4?C) used, indicatingthat these CD14 molecules were not taken up by an activeprocess.Conclusions: These data indicate the presence of a largeintracellular CD14 pool in monocytes with a yet unknownfunction, and suggest that LPS and CD14 molecules can beinternalized independently after association on the cellsurface.
Tárgyszavak:	Orvostudományok Klinikai orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban LPS internalization CD14
Megjelenés:	Cytometry 41 (2000), p. 279-288. -
További szerzők:	Poppelier, Miriam J. J. G Broekhuizen, Roel Verhoef, Jan Strijp, Jos A. G., van Kessel, Kok P. M., van
Internet cím:	Intézményi repozitóriumban (DEA) tárolt változat
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001-es BibID:	BIBFORM055878
Első szerző:	Antal-Szalmás Péter (laboratóriumi szakorvos)
Cím:	CD14/Fc fusion protein - an artificial antibody / Antal-Szalmás Péter, Vida András, Majoros László, Sümegi Andrea, Bácsi Attila, Vereb György, van Strijp Jos, van Kessel Kok
Dátum:	2012
Tárgyszavak:	Természettudományok Biológiai tudományok idézhető absztrakt
Megjelenés:	Cytometry. Part B, Clinical Cytometry 82 (2012), p. 410. -
További szerzők:	Vida András (1979-) (molekuláris biológus, genetikus) Majoros László (1966-) (szakorvos, klinikai mikrobiológus) Sümegi Andrea (1969-) (biológus) Bácsi Attila (1967-) (immunológus) Vereb György (1965-) (absztraktok, könyvfejezetek) Strijp, Jos A. G., van Kessel, Kok P. M., van
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001-es BibID:	BIBFORM038589
035-os BibID:	PMID:11590623
Első szerző:	Antal-Szalmás Péter (laboratóriumi szakorvos)
Cím:	A novel flow cytometric assay to quantify soluble CD14 concentration in human serum / Péter Antal-Szalmás, Ibolya Szöllősi, Gabriella Lakos, Emese Kiss, István Csípő, Andrea Sümegi, Sándor Sipka, Jos A. G. van Strijp, Kok P. M. van Kessel, Gyula Szegedi
Dátum:	2001
ISSN:	0196-4763
Megjegyzések:	BACKGROUND: CD14, the major lipopolysaccharide (LPS)-binding protein of myeloid cells, is found as a soluble molecule in human serum. Recent data describe the presence of elevated soluble CD14 (sCD14) concentration in various disorders, confirming disease activity. A novel, easy, and rapid flow cytometric assay was developed to measure sCD14 levels in serum. METHODS: The assay is based on the competition between membrane-expressed CD14 of isolated monocytes from healthy volunteers and sCD14 in the sample sera for binding to anti-CD14 monoclonal antibodies (mAb; 26ic or 60bca). The amount of cell-associated mAb is determined with a fluorescein isothiocyanate (FITC)-labeled anti-mouse conjugate and flow cytometry. The fluorescence signal is inversely proportional with the amount of serum sCD14. Using dilutions of a standard serum, the concentration of sCD14 in the samples is calculated and compared with results obtained by a commercial sCD14 enzyme-linked immunosorbent assay (ELISA). RESULTS: After optimization, the assay showed log-log linearity of 122.1-984.7 ng/ml sCD14 using mAb 26ic and 29.5-246.2 ng/ml sCD14 using mAb 60bca. It revealed similar results as the ELISA (mAb 26ic: r = 0.88, mAb 60bca: r = 0.92) and provided significantly elevated sCD14 levels in systemic lupus erythematosus patients compared with controls (26ic: 2,213 versus 1,676 ng/ml, P < 0.002; 60bca: 2,625 versus 1,907 ng/ml, P < 0.0002). Receiver operating characteristic curve analysis suggested a reasonable diagnostic efficacy of sCD14 quantification in this autoimmune disease. CONCLUSIONS: The method is easy, rapid, sensitive, and can be used in the follow-up of patients suffering from sepsis or chronic inflammatory disorders.
Tárgyszavak:	Orvostudományok Klinikai orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban egyetemen (Magyarországon) készült közlemény
Megjelenés:	Cytometry 45 : 2 (2001), p. 115-123. -
További szerzők:	Szöllősi Ibolya Lakos Gabriella (1963-) (laboratóriumi szakorvos, transzfúziológus, immunológus) Kiss Emese (1960-) (belgyógyász, immunológus) Csípő István (1953-) (vegyész) Sümegi Andrea (1969-) (biológus) Sipka Sándor (1945-) (laboratóriumi szakorvos) Strijp, Jos A. G., van Kessel, Kok P. M., van Szegedi Gyula (1936-2013) (belgyógyász, immunológus)
Internet cím:	Intézményi repozitóriumban (DEA) tárolt változat
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