Effect of prolactin on lymphocyte activation from systemic lupus erythematosus patients


Por: Chavez-Rueda K., Legorreta-Haquet V.Ma., Cervera-Castillo H., Sánchez L., Jara L.J., Zenteno E., Chavez-Sanchez L., Blanco-Favela F.

Publicada: 1 ene 2007
Resumen:
The aim was to explore the role of prolactin (PRL) in the lymphocyte activation process in systemic lupus erythematosus (SLE) patients in an in vitro model. Peripheral blood mononuclear cells (PBMCs) were isolated from SLE patients and healthy individuals. The mRNA for PRL and its receptor obtained by standard techniques, with an appropriate primer, were subjected to polymerase chain reaction (PCR) and visualized. The PBMCs were cultured with (a) medium alone as a negative control, (b) unspecific mitogen as a positive control, (c)PRLalone, (d) mitogen plus PRL, (e) mitogen plus antibody anti-PRL, and (f ) mitogen plus a nonrelated antibody. Then CD69 and CD154 were determined by flow cytometry analysis. Twelve inactive and 15 active SLE patients were studied. Twenty-five percent of the active patients displayed hyperprolactinemia. Under basal conditions CD69 expression was associated with disease activity. The PBMCs activated in vitro were capable of producing and secreting PRL, measured by mRNA and Nb2 assay. In a similar way, the mRNA for the PRL receptor was visualized. Cells from SLE patients cultivated with PRL alone did not display increased CD69 and CD154 expression. The addition of PRL to the unspecific stimulated culture does not have an additive effect. In contrast, the addition of antibodies against PRL in order to block the autocrine PRL resulted in a striking reduction of CD69 and CD154 expression. © 2007 New York Academy of Sciences.

Filiaciones:
Chavez-Rueda K.:
 Pediatric Hospital, Centro Medico Nacional Siglo XXI, IMSS, México, D.F., Mexico

Legorreta-Haquet V.Ma.:
 Pediatric Hospital, Centro Medico Nacional Siglo XXI, IMSS, México, D.F., Mexico

Cervera-Castillo H.:
 Rheumatology Department, HGZ25, IMSS, México, D.F., Mexico

Sánchez L.:
 Rheumatology Department, Hospital de Especialidades Centro Medico Nacional Siglo XXI, IMSS, México, D.F., Mexico

Jara L.J.:
 Rheumatology Department, Hospital de Especialidades Centro Medico Nacional la Raza, IMSS, México, D.F., Mexico

Zenteno E.:
 Biochemistry Department, Medicine Faculty, Autonomous National University of Mexico, UNAM, Mexico, D.F., Mexico

Chavez-Sanchez L.:
 Pediatric Hospital, Centro Medico Nacional Siglo XXI, IMSS, México, D.F., Mexico

Blanco-Favela F.:
 Pediatric Hospital, Centro Medico Nacional Siglo XXI, IMSS, México, D.F., Mexico

 Immunology Research Unit, Hospital de Pediatría, Centro Médico Nacional Siglo XXI, Av. Cuahutemoc 330 Col. Doctores, CP: 03020 IMSS, México, D.F., Mexico
ISSN: 00778923
Editorial
BLACKWELL PUBLISHING, 9600 GARSINGTON RD, OXFORD OX4 2DQ, OXEN, ENGLAND, Estados Unidos America
Tipo de documento: Conference Paper
Volumen: 1108 Número:
Páginas: 157-165
WOS Id: 000249051600018
ID de PubMed: 17893982