Murao Yoshinori, Isayama Kenji, Saito Fukuki, Hirakawa Akihiko, Nakatani Toshio
Department of Emergency and Critical Care Medicine, Kansai Medical University, Osaka 570-8507, Japan.
J Trauma. 2009 Nov;67(5):975-82. doi: 10.1097/TA.0b013e3181b83b7a.
Hemorrhagic shock and resuscitation induce immunosuppression. CD4CD25 regulatory T cells and gammadeltaT cells may affect these immunosuppressive conditions. Hypertonic saline resuscitation reduces damage to organs and apoptosis and also restores immunosuppressive condition. We investigated how hypertonic saline resuscitation affected the induction of CD4CD25 regulatory T cells and gammadeltaT cells, and their apoptosis after hemorrhagic shock and resuscitation, and its relationship to inducible nitric oxide synthase (iNOS) (nitric oxide production).
Male inbred C57BL6/J mice 8-week to 12-week-old as wild type and iNOS gene knock out (iNOS-/-), weighing 20 g to 35 g, were used. Hemorrhagic shock model of +/-40 mm Hg for 60 minutes was setup. Animals were randomly assigned to the following four resuscitation group: (1) wild HS: resuscitation with hypertonic saline (4 mL/Kg of 7.5% NaCl) and shed blood (SB), (2) wild 2LR: resuscitation with lactated Ringer's solution (two times the volume of the SB) and SB, (3) iNOS knockout HS, and (4) iNOS knockout 2LR. Untreated groups for wild and iNOS knockout mice were designated as control groups. Samples of thymus and spleen were harvested at 2 hours, 6 hours, 24 hours, and 48 hours after resuscitation. CD4CD25 regulatory T cells and gammadeltaT cells were analyzed using three-color flow cytometry.
(1) gammadelta T cells increased earlier at 24 hours and CD4CD25 regulatory T cells increased later at 48 hours compared with controls in spleen of wild type (p < 0.01). (2) Hypertonic saline resuscitation suppressed gammadelta T cells compared with 2LR at 24 hours in iNOS knockout mice in spleen (p < 0.05). Hypertonic saline resuscitation increased apoptosis of CD4CD25 regulatory T cells at 48 hours in iNOS knockout mice in spleen (p < 0.01). (3) CD4CD25 regulatory T cells of iNOS knockout both in HS and 2LR groups at 48 hours decreased compared with wild type both in HS and 2LR groups in spleen (p < 0.01). (4) Apoptotic gammadelta T cells both in spleen and thymus in iNOS knockout mice at 48 hours increased compared with those in wild type (p < 0.05, respectively, except gammadelta T cells 2LR in spleen: p = 0.058).
gammadelta T cells increased earlier at 24 hours, whereas CD4CD25 regulatory T cells increased later at 48 hours in spleen of wild type. Hypertonic saline was effective without the presence of iNOS, i.e., decreased gammadelta T cells at 24 hours and increased apoptosis of CD4CD25 regulatory T cells at 48 hours. CD4CD25 regulatory T cells at 48 hours without iNOS decreased compared with those of wild type. gammadelta T cells at 48 hours induced apoptosis under the condition without iNOS in spleen and thymus. iNOS worked as an accelerating factor for immunosuppressive condition, affected apoptosis, and immunoenhancing effect by hypertonic saline.
失血性休克及复苏可导致免疫抑制。CD4CD25调节性T细胞和γδT细胞可能影响这些免疫抑制状态。高渗盐水复苏可减少器官损伤和细胞凋亡,还可恢复免疫抑制状态。我们研究了高渗盐水复苏对失血性休克及复苏后CD4CD25调节性T细胞和γδT细胞的诱导、其凋亡的影响,以及与诱导型一氧化氮合酶(iNOS)(一氧化氮生成)的关系。
使用8至12周龄、体重20至35克的雄性近交系C57BL6/J小鼠作为野生型和iNOS基因敲除(iNOS-/-)小鼠。建立±40mmHg持续60分钟的失血性休克模型。动物被随机分为以下四个复苏组:(1)野生型高渗盐水组:用高渗盐水(4mL/Kg的7.5%NaCl)和自体失血(SB)进行复苏;(2)野生型乳酸林格液组:用乳酸林格液(SB体积的两倍)和SB进行复苏;(3)iNOS基因敲除高渗盐水组;(4)iNOS基因敲除乳酸林格液组。野生型和iNOS基因敲除小鼠的未处理组作为对照组。复苏后2小时、6小时、24小时和48小时采集胸腺和脾脏样本。使用三色流式细胞术分析CD4CD25调节性T细胞和γδT细胞。
(1)与野生型对照组相比,野生型脾脏中γδT细胞在24小时时较早增加,而CD4CD25调节性T细胞在48小时时较晚增加(p<0.01)。(2)在iNOS基因敲除小鼠脾脏中,与乳酸林格液复苏组相比,高渗盐水复苏在24小时时抑制了γδT细胞(p<0.05)。在iNOS基因敲除小鼠脾脏中,高渗盐水复苏在48小时时增加了CD4CD25调节性T细胞的凋亡(p<0.01)。(3)与野生型高渗盐水组和乳酸林格液组相比,iNOS基因敲除高渗盐水组和乳酸林格液组在48小时时的CD4CD25调节性T细胞均减少(p<0.01)。(4)与野生型相比,iNOS基因敲除小鼠在48小时时脾脏和胸腺中的γδT细胞凋亡均增加(脾脏中γδT细胞乳酸林格液组除外,p = 0.058,其余p<0.05)。
野生型脾脏中γδT细胞在24小时时较早增加,而CD4CD25调节性T细胞在48小时时较晚增加。在没有iNOS的情况下,高渗盐水是有效的,即在24小时时减少γδT细胞,在48小时时增加CD4CD25调节性T细胞的凋亡。与野生型相比,48小时时没有iNOS的情况下CD4CD25调节性T细胞减少。在没有iNOS的情况下,48小时时脾脏和胸腺中的γδT细胞诱导凋亡。iNOS作为免疫抑制状态的加速因子,影响细胞凋亡以及高渗盐水的免疫增强作用。