Franco-Martínez S, Niño-Moreno P, Bernal-Silva S, Baranda L, Rocha-Meza M, Portales-Cervantes L, Layseca-Espinosa E, González-Amaro R, Portales-Pérez D
Department of Immunology, Facultad de Medicina, UASLP, San Luis Potosí, SLP, Mexico.
Clin Exp Immunol. 2006 Nov;146(2):253-61. doi: 10.1111/j.1365-2249.2006.03213.x.
P2X(7) is a channel receptor gated by adenosine triphosphate (ATP) that is involved in the killing of intracellular mycobacteria. To explore further the role of P2X(7) in immunity against Mycobacterium tuberculosis, we studied its expression and function in 19 patients with pulmonary tuberculosis (TB) and 19 healthy contacts. Flow cytometry analysis showed a similar and variable expression of P2X(7) in TB patients and healthy subjects. In contrast, P2X(7) mARN levels were significantly higher in TB patients. When the function of the P2X(7) receptor in peripheral blood mononuclear cells (PBMC) was assessed by the effect of exogenous ATP on apoptosis, the uptake of the fluorescent marker Lucifer yellow or extracellular signal regulated kinase (ERK) phosphorylation, no significant differences were detected in patients and controls. However, mRNA macroarray analysis showed that upon stimulation with ATP, the PBMC from TB patients showed a significant induction of a higher number of cytokine genes (27 of 96), and a lower number of apoptosis genes (20 of 96) compared to healthy controls (17 and 76 genes, respectively). These results suggest that although the PBMC from TB patients do not show apparent abnormalities in the expression of P2X(7), and the intracellular signals generated through it, the pattern of gene expression induced by ATP in these cells is different from that found in healthy contacts. This phenomenon suggests a defective function of P2X(7) in the immune cells from TB patients, a condition that may contribute to the inability of these patients to eliminate the mycobacteria.
P2X(7)是一种由三磷酸腺苷(ATP)门控的通道受体,参与细胞内分枝杆菌的杀伤。为了进一步探究P2X(7)在抗结核分枝杆菌免疫中的作用,我们研究了其在19例肺结核患者和19名健康接触者中的表达及功能。流式细胞术分析显示,肺结核患者和健康受试者中P2X(7)的表达相似但存在差异。相比之下,肺结核患者中P2X(7)的mRNA水平显著更高。当通过外源性ATP对凋亡的影响、荧光标记物路西法黄的摄取或细胞外信号调节激酶(ERK)磷酸化来评估外周血单核细胞(PBMC)中P2X(7)受体的功能时,患者和对照组之间未检测到显著差异。然而,mRNA芯片分析显示,与健康对照组(分别为17个和76个基因)相比,用ATP刺激后,肺结核患者的PBMC中更多数量的细胞因子基因(96个中的27个)被显著诱导,而凋亡基因数量较少(96个中的20个)。这些结果表明,尽管肺结核患者的PBMC在P2X(7)的表达及其产生的细胞内信号方面未显示明显异常,但这些细胞中由ATP诱导的基因表达模式与健康接触者不同。这种现象表明肺结核患者免疫细胞中的P2X(7)功能存在缺陷,这种情况可能导致这些患者无法清除分枝杆菌。