effect of the monocyte locomotion inhibitory factor (mlif) a natural anti-inflammatory produced by e. histolytica on apoptosis in human cd4 + t lymphocytes单核细胞运动的影响抑制因子(mlif)产生的一种天然的抗炎大肠阿米巴在人类cd4 + t淋巴细胞凋亡.pdfVIP

effect of the monocyte locomotion inhibitory factor (mlif) a natural anti-inflammatory produced by e. histolytica on apoptosis in human cd4 + t lymphocytes单核细胞运动的影响抑制因子(mlif)产生的一种天然的抗炎大肠阿米巴在人类cd4 + t淋巴细胞凋亡.pdf

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effectofthemonocytelocomotioninhibitoryfactor(mlif)anaturalanti-inflammatoryproducedbye.histolyticaonapoptosisinhumancd4tlymphocytes单核细胞运动的影响抑制因子(mlif)产生的一种天然的抗炎大肠阿米巴在人类cd4t淋巴细胞凋亡

Pharmacology Pharmacy, 2011, 2, 248-255 doi:10.4236/pp.2011.24032 Published Online October 2011 (http://www.SciRP.org/journal/pp) Effect of the Monocyte Locomotion Inhibitory Factor (MLIF) a Natural Anti-Inflammatory Produced by E. histolytica on Apoptosis in Human CD4+ T Lymphocytes 1 2 1 Sara Rojas-Dotor , Liliana Vargas-Neri , Francisco Blanco-Favela 1Unidad de Investigación Médica en Inmunología, Hospital de Pediatría, Centro Médico Nacional Siglo XXI Instituto Mexicano del Seguro Social, México City, México; 2Facultad de Química, Universidad Nacional Autónoma de México, México City, México. Email: srdotor@.mx Received June 4th, 2011; revised July 28th, 2011; accepted August 16th, 2011. ABSTRACT Apoptosis prevents the extravasation of intracellular material and the subsequent inflammatory response. Currently , it is not known whether Monocyte Locomotion Inhibitor Factor (MLIF), an anti-inflammatory pentapeptide, induces pro- grammed cell death. We evaluated the effect of MLIF on extrinsic and intrinsic apoptosis pathways human CD4+ T lymphocytes. Cells were cultured for 24 h in RPMI-1640 medium alone (control) or in RPMI medium containing MLIF alone, PMA alone, PMA + MLIF or actinomycin D. Annexin V/propidium iodide-stained cells in early apoptosis showed that cells treated with MLIF or PMA + MLIF were not significantly different from control cells in medium; in contrast, cells treated with PMA or PMA + MLIF demonstrated significant differences from the control in delayed apoptosis. Cytochrome c and caspase 3 levels in cells treated with MLIF showed no significant differences from control cells, however, compared to the control, cells treated with PMA and PMA + MLIF exhibited a significant increase in cytochrome c and caspase 3 levels, which demonstrates that this weak induction of cell death is re

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