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huIL33 Mouse
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huIL33 Mouse
製品名
huIL33 Mouse
製品ID
C001722
系統名
C57BL/6NCya-Il33em1(hIL33)/Cya
背景情報
C57BL/6NCya
状況
このマウス系統を論文で使用する場合は、「huIL33 Mouse(カタログ番号C001722)はサイアジェンから購入しました。」と引用してください。
HUGO-GT Humanized Models
Immune Target Humanized Mouse Models
Cytokine Gene Humanized Mouse Models
Safe Harbor Knock-in
製品タイプ
年齢
遺伝子型
性別
数量
標準的な配送方法では、少なくとも3匹のヘテロ接合体キャリアを保証しています。ホモ接合体キャリアや指定された性別の個体の繁殖サービスも利用可能です。
お見積もりについてはこちらまでご連絡ください
HUGO-GT Humanized Models
Immune Target Humanized Mouse Models
Cytokine Gene Humanized Mouse Models
Safe Harbor Knock-in
基本情報
検証 Data
関連リソース
基本情報
遺伝子名
遺伝子別名
DVS27, IL1F11, NF-HEV, NFEHEV, C9orf26
NCBI ID
染色体
Chr 9
MGI ID
さらに
系統詳細
IL33 encodes interleukin-33 (IL-33), a member of the IL-1 cytokine family that operates as a crucial "alarmin" molecule within the immune system [1]. Released by epithelial and endothelial cells, as well as other cell types, upon cellular damage or stress, IL-33 signals through its receptor, the IL1RL1/ST2 heterodimer, expressed on various immune cells, including Th2 cells, mast cells, basophils, eosinophils, and innate lymphoid cells type 2 (ILC2s). Receptor engagement activates downstream signaling pathways, notably NF-κB and MAPK, culminating in the production of type 2 cytokines such as IL-4, IL-5, and IL-13, thereby promoting Th2 cell differentiation and orchestrating type 2 immune responses critical for defense against helminths and in allergic inflammation [1-2]. Constitutive expression of IL-33 in barrier tissues positions it as a sentinel, contributing to tissue homeostasis and rapidly responding to environmental insults [3]. Aberrant expression and signaling of IL-33 have been strongly implicated in the pathogenesis of a spectrum of inflammatory conditions, including asthma, atopic dermatitis, allergic rhinitis, and inflammatory bowel disease, highlighting its significance as a potential therapeutic target in these disorders [4].
The huIL33 mouse is a humanized model constructed by replacing the sequence of the mouse Il33 gene in situ with the corresponding sequence from the human IL33 gene. The huIL33 mice can be used for studies on asthma, atopic dermatitis, allergic rhinitis, inflammatory bowel disease, and other inflammatory disorders, as well as for IL33-targeted drug development.
参考文献
Shakerian L, Kolahdooz H, Garousi M, Keyvani V, Kamal Kheder R, Abdulsattar Faraj T, Yazdanpanah E, Esmaeili SA. IL-33/ST2 axis in autoimmune disease. Cytokine. 2022 Oct;158:156015.
Kudo-Saito C, Miyamoto T, Imazeki H, Shoji H, Aoki K, Boku N. IL33 Is a Key Driver of Treatment Resistance of Cancer. Cancer Res. 2020 May 15;80(10):1981-1990.
Zhou Z, Yan F, Liu O. Interleukin (IL)-33: an orchestrator of immunity from host defence to tissue homeostasis. Clin Transl Immunology. 2020 Jun 17;9(6):e1146.
Cayrol C. IL-33, an Alarmin of the IL-1 Family Involved in Allergic and Non Allergic Inflammation: Focus on the Mechanisms of Regulation of Its Activity. Cells. 2021 Dec 30;11(1):107.
系統作製戦略
The sequences from ATG start codon to TAA stop codon of the endogenous mouse Il33 gene were replaced with the sequences from ATG start codon to TAG stop codon of the human IL33 gene.

Figure 1. Gene editing strategy of huIL33 Mice.
適用分野
IL33-targeted drug screening, development, and evaluation;
Research on the pathological mechanisms and therapeutic approaches of asthma, atopic dermatitis, allergic rhinitis, and inflammatory bowel disease;
Research on other inflammatory disorders.
検証 Data
1. Gene Expression
Lung, spleen, liver, and brain tissues were harvested from huIL33 and wild-type (WT) mice. Specific primers were used to detect human IL33 and mouse Il33 transcripts, with mGapdh serving as the internal control for calculating relative gene expression. Data are presented as mean ± SD. RT-qPCR results showed that human IL33 transcripts were detected in the lung, spleen, liver, and brain tissues of huIL33 mice, while mouse Il33 transcripts were undetectable. Conversely, WT mouse tissues expressed mouse Il33 but showed no detectable human IL33 expression. Based on the CT values, huIL33 mice may exhibit low expression levels.

Figure 2. RT-qPCR analysis of human IL33 and mouse Il33 transcript levels in the lung, spleen, liver, and brain of huIL33 and wild-type (WT) mice (7 weeks old, female, n=3).
2. Protein Expression
After intraperitoneal injection of LPS (10 mg/kg) for 4–6 hours, lung tissues were harvested from huIL33 mice and wild-type (WT) mice, followed by tissue homogenization. The protein expression levels of human IL-33 and murine IL-33 in the lung homogenate supernatants were measured by ELISA. Data are presented as mean±SD. ELISA results showed that human IL-33 protein was detected in the lung homogenate supernatants of huIL33 mice. A low level of human IL-33 was also detected in the lung homogenate supernatants of WT mice, which may be attributed to low-level cross-reactivity of the ELISA kit with endogenous murine IL-33, combined with the high sensitivity of the assay, resulting in a weak positive signal. Murine IL-33 protein was detectable in the lung homogenate supernatants of WT mice but was undetectable in those of huIL33 mice.

Figure 3. ELISA detection of human and murine IL33 protein expression in lung tissues from huIL33 and wild-type (WT) mice (6-week-old, female, n=5).
関連リソース
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