Reindl Wolfgang, Weiss Susanne, Lehr Hans-Anton, Förster Irmgard
II Medizinische Klinik and Poliklinik, Klinikum rechts der Isar, Munich, Germany.
Immunology. 2007 Jan;120(1):19-27. doi: 10.1111/j.1365-2567.2006.02473.x.
Dysregulated cytokine responsiveness by myeloid cells can be a trigger for the development of chronic inflammation as well as inflammatory bowel disease. Thus, mice with a myeloid-specific defect in signal transducer and activator of transcription (Stat) 3 develop spontaneous colitis secondary to the inability of myeloid cells to respond to the immunosuppressive cytokine interleukin-10. We now examined whether the inflammation caused by Stat3-deficient macrophages is cell autonomous or dependent on their interaction with lymphocytes. For this purpose, myeloid-specific Stat3-deficient mice (LysMcre/Stat3(flox) mice) were intercrossed with RAG-1 knockout mice to generate LysMcre/Stat3(flox) RAG(-/-) mice. In these mutants and LysMcre/Stat3(flox) littermate control mice we determined the onset and severity of spontaneous chronic enterocolitis, and the reaction to dextran sodium sulphate (DSS)-induced epithelial damage, as well as to lipopolysaccharide (LPS) challenge. In contrast to LysMcre/Stat3(flox) mice, LysMcre/Stat3(flox) RAG(-/-) animals are protected from chronic enterocolitis. Although they respond to oral dextran sulphate with acute colitis symptoms, the inflammation heals similarly to wild type mice whereas LysMcre/Stat3(flox) mice exhibit continued colitis pathology. In addition, the hyperreactivity of LysMcre/Stat3(flox) mice to LPS-challenge in vivo was less severe in the absence of lymphocytes. Despite clear differences in the strength of inflammatory responses, macrophages of both LysMcre/Stat3(flox) mice and LysMcre/Stat3(flox) RAG(-/-) animals exhibited increased costimulatory capacity. In conclusion, our findings demonstrate that Stat3-deficient myeloid cells alone are not capable of inducing the severe pathology seen in LysMcre/Stat3(flox) mice. Yet when these cells can interact with lymphocytes their increased costimulatory potential will trigger an overshooting inflammatory response.
髓样细胞细胞因子反应失调可能是慢性炎症以及炎症性肠病发展的触发因素。因此,转录信号转导子与激活子(Stat)3存在髓样特异性缺陷的小鼠会继发自发性结肠炎,这是由于髓样细胞无法对免疫抑制性细胞因子白细胞介素-10作出反应所致。我们现在研究了Stat3缺陷型巨噬细胞引起的炎症是细胞自主性的还是依赖于它们与淋巴细胞的相互作用。为此,将髓样特异性Stat3缺陷型小鼠(LysMcre/Stat3(flox)小鼠)与RAG-1基因敲除小鼠杂交,以产生LysMcre/Stat3(flox) RAG(-/-)小鼠。在这些突变体和LysMcre/Stat3(flox)同窝对照小鼠中,我们确定了自发性慢性小肠结肠炎的发病情况和严重程度,以及对葡聚糖硫酸钠(DSS)诱导的上皮损伤、脂多糖(LPS)刺激的反应。与LysMcre/Stat3(flox)小鼠不同,LysMcre/Stat3(flox) RAG(-/-)动物可免受慢性小肠结肠炎的影响。尽管它们对口服葡聚糖硫酸钠会出现急性结肠炎症状,但炎症的愈合情况与野生型小鼠相似,而LysMcre/Stat3(flox)小鼠则表现出持续的结肠炎病理变化。此外,在没有淋巴细胞的情况下,LysMcre/Stat3(flox)小鼠体内对LPS刺激的高反应性也不那么严重。尽管炎症反应强度存在明显差异,但LysMcre/Stat3(flox)小鼠和LysMcre/Stat3(flox) RAG(-/-)动物的巨噬细胞共刺激能力均有所增强。总之,我们的研究结果表明,仅Stat3缺陷的髓样细胞不足以诱发LysMcre/Stat3(flox)小鼠中所见的严重病理变化。然而,当这些细胞能够与淋巴细胞相互作用时,其增强的共刺激潜能将引发过度的炎症反应。