首页 / 产品 / 蛋白 / 细胞因子、趋化因子与生长因子
纯度 | >95%SDS-PAGE. |
种属 | Human |
靶点 | IL22 |
Uniprot No | Q9GZX6 |
内毒素 | < 0.01EU/μg |
表达宿主 | E.coli |
表达区间 | 34-179aa |
氨基酸序列 | APISSHCRLD KSNFQQPYIT NRTFMLAKEA SLADNNTDVR LIGEKLFHGV SMSERCYLMK QVLNFTLEEV LFPQSDRFQP YMQEVVPFLA RLSNRLSTCH IEGDDLHIQR NVQKLKDTVK KLGESGEIKA IGELDLLFMS LRNACI |
预测分子量 | 17 kDa |
蛋白标签 | His tag N-Terminus |
缓冲液 | PBS, pH7.4, containing 0.01% SKL, 1mM DTT, 5% Trehalose and Proclin300. |
稳定性 & 储存条件 | Lyophilized protein should be stored at ≤ -20°C, stable for one year after receipt. Reconstituted protein solution can be stored at 2-8°C for 2-7 days. Aliquots of reconstituted samples are stable at ≤ -20°C for 3 months. |
复溶 | Always centrifuge tubes before opening.Do not mix by vortex or pipetting. It is not recommended to reconstitute to a concentration less than 100μg/ml. Dissolve the lyophilized protein in distilled water. Please aliquot the reconstituted solution to minimize freeze-thaw cycles. |
以下是关于IL-22重组蛋白的3篇代表性文献及其简要摘要:
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1. **文献名称**: *Interleukin-22: A cytokine produced by T, NK and NKT cell subsets, with importance in the innate immune defense and tissue protection*
**作者**: Sabat R, et al.
**摘要**: 该文献总结了IL-22的生物学功能,指出其由Th17、NK等细胞分泌,通过激活STAT3信号通路在黏膜屏障防御(如肠道、皮肤)中起关键作用,同时强调重组IL-22在实验模型中可减轻炎症并促进上皮修复。
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2. **文献名称**: *Therapeutic efficacy of IL-22 in experimental colitis: Role of STAT3 activation and microbiota regulation*
**作者**: Pickert G, et al.
**摘要**: 研究使用重组IL-22治疗小鼠结肠炎模型,发现其通过STAT3依赖机制增强肠上皮细胞再生,减少肠道通透性,并通过调节肠道菌群平衡缓解炎症,提示其作为炎症性肠病治疗潜力。
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3. **文献名称**: *IL-22 promotes fibroblast-mediated wound repair in the skin*
**作者**: Sugimoto K, et al.
**摘要**: 该研究证明重组IL-22通过激活皮肤成纤维细胞,促进胶原合成和角质形成细胞迁移,加速小鼠皮肤损伤修复,揭示了IL-22在慢性伤口愈合中的潜在应用价值。
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**备选文献**(如需第四篇):
4. **文献名称**: *Recombinant IL-22 protects against acetaminophen-induced liver injury via modulation of oxidative stress pathways*
**作者**: Ki SH, et al.
**摘要**: 实验显示重组IL-22通过上调抗氧化基因(如Nrf2)减轻对乙酰氨基酚诱导的小鼠肝损伤,抑制肝细胞凋亡并促进再生,提示其作为药物性肝损伤治疗的策略。
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以上文献涵盖IL-22在黏膜免疫、肠道炎症、皮肤修复及肝脏保护中的核心机制与应用,均为领域内经典研究。如需具体DOI或期刊年份可进一步补充。
Interleukin-22 (IL-22) is a member of the IL-10 cytokine family, primarily produced by immune cells such as T helper 17 (Th17) cells, group 3 innate lymphoid cells (ILC3s), and natural killer (NK) cells. It plays a dual role in modulating inflammatory responses and promoting tissue repair by targeting epithelial and stromal cells. Unlike many interleukins, IL-22 does not directly regulate immune cells but acts on non-hematopoietic cells expressing the IL-22 receptor complex (IL-22R1 and IL-10R2). This receptor is abundant at barrier surfaces, including the skin, gut, and lungs, making IL-22 critical for maintaining mucosal integrity, antimicrobial defense, and wound healing.
Recombinant IL-22 (rIL-22) is engineered through genetic cloning, often using mammalian or bacterial expression systems, to produce bioactive forms of the protein for research and therapeutic applications. Its therapeutic potential lies in its ability to enhance epithelial regeneration and mitigate damage in conditions like inflammatory bowel disease (IBD), acute liver injury, and pancreatitis. Preclinical studies highlight its efficacy in reducing mucosal inflammation and promoting tissue repair in animal models. However, IL-22's role is context-dependent; excessive or dysregulated signaling can exacerbate pathologies, such as psoriasis or certain cancers, by driving hyperproliferation or chronic inflammation.
Current research focuses on optimizing rIL-22 delivery and understanding its pleiotropic effects. Clinical trials explore its use in combination therapies or as a standalone treatment for gastrointestinal and metabolic disorders. Challenges include balancing its protective versus pro-inflammatory outcomes and minimizing off-target effects. Advances in protein engineering, such as PEGylation or fusion proteins, aim to improve its stability and bioavailability. As a therapeutic agent, rIL-22 represents a promising yet complex candidate, bridging immunology and regenerative medicine, with ongoing studies refining its clinical applications.
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