Zhang Yijia, Wang Zixu, Dong Yulan, Cao Jing, Chen Yaoxing
Laboratory of Anatomy of Domestic Animals, College of Veterinary Medicine, China Agricultural University, Beijing 100193, China.
Antioxidants (Basel). 2022 Apr 8;11(4):748. doi: 10.3390/antiox11040748.
Previous studies found that melatonin modulates a combination of green-and-blue-light-induced B-lymphocyte proliferation via its membrane receptors Mel1a and Mel1c. However, in addition to its membrane-bound receptors, melatonin also functions through binding to nuclear receptors RORα/RORβ/RORγ. In this study, we raised 120 chicks under 400-700 nm white (WW), 660 nm red (RR), 560 nm green (GG) and 480 nm blue light (BB) from P0 to P26. From P27 to P42, half of the chickens in green, blue and red were switched to blue (G→B), green (B→G) and red (R→B), respectively. We used immunohistochemistry, Western blotting, qRT-PCR, Elisa and MTT to investigate the influence of various monochromatic light combinations on the bursal B lymphocyte apoptosis and oxidative stress levels as well as estimate whether melatonin and its nuclear receptors were involved in this process. Consistent with the increase in the plasma melatonin concentration and antioxidant enzyme activity, we observed that G→B significantly decreased the , mRNA level, inhibited Bax, Caspase-3 and p-iκb, p-p65 protein expression, increased the IL-10 level and Nrf2, HO-1 protein expression, down-regulated the MDA and pro-inflammatory IL-6, TNF-α and IFN-γ levels in the bursa compared with WW, RR, GG, BB and R→B, respectively. Our in vitro results showed exogenous melatonin supplementation inhibited B-lymphocyte apoptosis, decreased IL-6, TNF-α, IFN-γ and ROS production, down-regulated , mRNA level and p-iκb and p-p65 protein expression, whereas it improved the IL-10 level and Nrf2 and the HO-1 protein expression in bursal B lymphocyte. Moreover, these responses were abrogated by RORα agonist SR1078 but were mimicked by RORα antagonist SR3335 or RORγ antagonist GSK2981278. In addition, p65 antagonist BAY reversed RORα/RORγ-mediated G→B-inhibited bursal B lymphocyte apoptosis. Overall, we concluded that melatonin nuclear RORα/RORγ mediates G→B-inhibited bursal B lymphocyte apoptosis via reducing oxidative stress and Nfκb expression.
先前的研究发现,褪黑素通过其膜受体Mel1a和Mel1c调节绿光和蓝光诱导的B淋巴细胞增殖。然而,除了其膜结合受体外,褪黑素还通过与核受体RORα/RORβ/RORγ结合发挥作用。在本研究中,我们将120只雏鸡从P0饲养至P26,饲养环境为400 - 700 nm白光(WW)、660 nm红光(RR)、560 nm绿光(GG)和480 nm蓝光(BB)。从P27至P42,绿色、蓝色和红色组中的半数鸡分别转换至蓝光(G→B)、绿光(B→G)和红光(R→B)环境。我们使用免疫组织化学、蛋白质免疫印迹法、qRT-PCR、酶联免疫吸附测定和MTT法来研究各种单色光组合对法氏囊B淋巴细胞凋亡和氧化应激水平的影响,并评估褪黑素及其核受体是否参与此过程。与血浆褪黑素浓度和抗氧化酶活性的增加一致,我们观察到与WW、RR、GG、BB和R→B相比,G→B显著降低了 、 mRNA水平,抑制了Bax、Caspase-3以及p-iκb、p-p65蛋白表达,增加了IL-10水平以及Nrf2、HO-1蛋白表达,下调了法氏囊中MDA以及促炎细胞因子IL-6、TNF-α和IFN-γ水平。我们的体外实验结果表明,外源性补充褪黑素可抑制B淋巴细胞凋亡,降低IL-6、TNF-α、IFN-γ和ROS的产生,下调 、 mRNA水平以及p-iκb和p-p65蛋白表达,同时提高法氏囊B淋巴细胞中IL-10水平以及Nrf2和HO-1蛋白表达。此外,RORα激动剂SR1078消除了这些反应,但RORα拮抗剂SR3335或RORγ拮抗剂GSK2981278模拟了这些反应。此外,p65拮抗剂BAY逆转了RORα/RORγ介导的G→B对法氏囊B淋巴细胞凋亡的抑制作用。总体而言,我们得出结论,褪黑素核受体RORα/RORγ通过降低氧化应激和Nfκb表达介导G→B对法氏囊B淋巴细胞凋亡的抑制作用。