Up-regulation of fas and fasL pro-apoptotic genes expression in type 1 diabetes patients after autologous haematopoietic stem cell transplantation


Autoria(s): de Oliveira, G. L. V.; Malmegrim, K. C. R.; Ferreira, A. F.; Tognon, R.; Kashima, S.; Couri, C. E. B.; Covas, D. T.; Voltarelli, J. C.; de Castro, F. A.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

14/10/2013

14/10/2013

2012

Resumo

Type 1 diabetes (T1D) is a chronic autoimmune disease characterized by T cell-mediated destruction of pancreatic beta cells, resulting in insulin deficiency and hyperglycaemia. Recent studies have described that apoptosis impairment during central and peripheral tolerance is involved in T1D pathogenesis. In this study, the apoptosis-related gene expression in T1D patients was evaluated before and after treatment with high-dose immunosuppression followed by autologous haematopoietic stem cell transplantation (HDI-AHSCT). We also correlated gene expression results with clinical response to HDI-AHSCT. We observed a decreased expression of bad, bax and fasL pro-apoptotic genes and an increased expression of a1, bcl-xL and cIAP-2 anti-apoptotic genes in patients' peripheral blood mononuclear cells (PBMCs) compared to controls. After HDI-AHSCT, we found an up-regulation of fas and fasL and a down-regulation of anti-apoptotic bcl-xL genes expression in post-HDI-AHSCT periods compared to pre-transplantation. Additionally, the levels of bad, bax, bok, fasL, bcl-xL and cIAP-1 genes expression were found similar to controls 2 years after HDI-AHSCT. Furthermore, over-expression of pro-apoptotic noxa at 540 days post-HDI-AHSCT correlated positively with insulin-free patients and conversely with glutamic acid decarboxylase autoantibodies (GAD65) autoantibody levels. Taken together, the results suggest that apoptosis-related genes deregulation in patients' PBMCs might be involved in breakdown of immune tolerance and consequently contribute to T1D pathogenesis. Furthermore, HDI-AHSCT modulated the expression of some apoptotic genes towards the levels similar to controls. Possibly, the expression of these apoptotic molecules could be applied as biomarkers of clinical remission of T1D patients treated with HDI-AHSCT therapy.

Brazilian governmental agency: Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES, Coordination of the Advancement of Higher Education)

Brazilian governmental agency: Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES, Coordination of the Advancement of Higher Education)

Brazilian governmental agency: Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP, Foundation for the Support of Research in the State of Sao Paulo)

Brazilian governmental agency: Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP, Foundation for the Support of Research in the State of Sao Paulo)

Fundacao Hemocentro de Ribeirao Preto (FUNDHERP, Ribeirao Preto Blood Bank Foundation)

Fundacao Hemocentro de Ribeirao Preto (FUNDHERP, Ribeirao Preto Blood Bank Foundation)

Identificador

CLINICAL AND EXPERIMENTAL IMMUNOLOGY, MALDEN, v. 168, n. 3, supl. 1, Part 3, pp. 291-302, JUN, 2012

0009-9104

http://www.producao.usp.br/handle/BDPI/34491

10.1111/j.1365-2249.2012.04583.x

http://dx.doi.org/10.1111/j.1365-2249.2012.04583.x

Idioma(s)

eng

Publicador

WILEY-BLACKWELL

MALDEN

Relação

CLINICAL AND EXPERIMENTAL IMMUNOLOGY

Direitos

closedAccess

Copyright WILEY-BLACKWELL

Palavras-Chave #APOPTOSIS-RELATED GENES EXPRESSION #AUTOLOGOUS HAEMATOPOIETIC STEM CELL TRANSPLANTATION #BCL-2 FAMILY MEMBERS #DEATH RECEPTORS FAMILY MEMBERS #INHIBITORY APOPTOSIS PROTEINS #TYPE 1 DIABETES #SYSTEMIC-LUPUS-ERYTHEMATOSUS #ANTI-THYMOCYTE GLOBULIN #BCL-2 FAMILY PROTEINS #MULTIPLE-SCLEROSIS #NOD MICE #T-CELLS #RHEUMATOID-ARTHRITIS #AUTOIMMUNE-DISEASES #CENTRAL TOLERANCE #B-CELLS #IMMUNOLOGY
Tipo

article

original article

publishedVersion