The antiproliferative effect of a synthetic octapeptide, somatostatin analogue SMS 201-995 (SMS), and its capacity to bind were evaluated on human peripheral blood lymphocytes (PBL) activated by phytohemoagglutinin (PHA). We then addressed our work to investigate if SMS inhibits PHA activation of PBL by a cytostatic rather than a cytotoxic mechanism. Consequently, we studied the cell cycle distribution and the activation of caspase-3, measuring the presence of the cleavage product of poly(ADP-ribose) polymerases (PARP), and we evaluated the presence of apoptotic DNA by using a monoclonal antibody specific for the single-stranded regions of DNA. All our results indicate that SMS induces apoptosis in activated lymphocytes.

The apoptotic effect of somatostatin analogue SMS 201-995 on human lymphocytes / D. Lattuada, C. Casnici, A. Venuto, O. Marelli. - In: JOURNAL OF NEUROIMMUNOLOGY. - ISSN 0165-5728. - 133:1-2(2002 Dec), pp. 211-216. [10.1016/S0165-5728(02)00364-8]

The apoptotic effect of somatostatin analogue SMS 201-995 on human lymphocytes

D. Lattuada
Primo
;
O. Marelli
Ultimo
2002

Abstract

The antiproliferative effect of a synthetic octapeptide, somatostatin analogue SMS 201-995 (SMS), and its capacity to bind were evaluated on human peripheral blood lymphocytes (PBL) activated by phytohemoagglutinin (PHA). We then addressed our work to investigate if SMS inhibits PHA activation of PBL by a cytostatic rather than a cytotoxic mechanism. Consequently, we studied the cell cycle distribution and the activation of caspase-3, measuring the presence of the cleavage product of poly(ADP-ribose) polymerases (PARP), and we evaluated the presence of apoptotic DNA by using a monoclonal antibody specific for the single-stranded regions of DNA. All our results indicate that SMS induces apoptosis in activated lymphocytes.
Anti-Inflammatory Agents; Apoptosis; Humans; Caspase 3; Octreotide; Lymphocytes; Caspases; Chemotaxis, Leukocyte; Immunosuppressive Agents; Somatostatin; Cells, Cultured; Adult; DNA; Proteins; Middle Aged; Cell Cycle
Settore BIO/14 - Farmacologia
dic-2002
29-ott-2002
Article (author)
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/186710
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