The Harold L. Dorris Neurological Research Institute, Department of Molecular and Integrative Neurosciences, The Scripps Research Institute, La Jolla, CA 92037, USA.
Cytokine. 2011 Mar;53(3):311-9. doi: 10.1016/j.cyto.2010.11.017. Epub 2010 Dec 21.
CC Chemokine ligand 22 (Ccl22) is a selective, high affinity ligand at the CC chemokine receptor 4 (Ccr4). We have identified cDNAs encoding both ligand and receptor of the Ccl22-Ccr4 pair in cDNA libraries of the anterior hypothalamus/pre-optic area (AH/POA) by PCR. The AH/POA is the key brain region where endogenous pyrogens have been shown to act on warm sensitive neurons to affect thermogenesis in brown adipose tissue (BAT) and other thermogenically responsive tissues. We show that functional Ccr4 receptors are present in the AH/POA neurons as injection of Ccl22 into the POA but not to other hypothalamic nuclei induces an increase in core body temperature as measured by radiotelemetry. Indomethacin (5 mg/kg s.c) pre-treatment markedly reduced the hyperthermia evoked by POA injection of Ccl22 (10 ng/0.5 ul) and thus suggests that this hyperthermia is mediated through cyclooxygenase activation and thus likely through the formation and action of the pyrogen prostaglandin E2. The temperature elevation involves a decrease in the respiratory exchange ratio and increased activation of the brown adipose tissue as demonstrated by ¹⁸F-FDG-PET imaging. We describe a novel role to the ligand Ccl22 and its receptor Ccr4 in the anterior hypothalamus in temperature regulation that depends on the synthesis of the endogenous pyrogen, prostaglandin E2.
CC 趋化因子配体 22(Ccl22)是 CC 趋化因子受体 4(Ccr4)的选择性、高亲和力配体。我们通过 PCR 从下丘脑前区/视前区(AH/POA)的 cDNA 文库中鉴定出 Ccl22-Ccr4 对的配体和受体的 cDNA。AH/POA 是内源性热原作用于热敏神经元以影响棕色脂肪组织(BAT)和其他热敏组织产热的关键脑区。我们表明,功能性 Ccr4 受体存在于 AH/POA 神经元中,因为 Ccl22 注射到 POA 而不是其他下丘脑核中会导致核心体温升高,如放射性遥测测量所示。吲哚美辛(5mg/kg sc)预处理显著减少了 POA 注射 Ccl22(10ng/0.5μl)引起的高热,这表明这种高热是通过环氧化酶激活介导的,因此可能是通过形成和作用热原前列腺素 E2 介导的。体温升高涉及呼吸交换率降低和棕色脂肪组织的激活增加,如 ¹⁸F-FDG-PET 成像所示。我们描述了配体 Ccl22 和其受体 Ccr4 在调节体温方面在前下丘脑的新作用,这取决于内源性热原前列腺素 E2 的合成。