Rbpj-flox Mouse
一般名
Rbpj-flox
製品ID
S-CKO-18031
背景情報
C57BL/6JCya
系統ID
CKOCMP-19664-Rbpj-B6J-VB
状況
このマウス系統を論文で使用する場合は、「Rbpj-flox Mouse(カタログ番号S-CKO-18031)はサイアジェンから購入しました。」と引用してください。
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。
基本情報
系統名
Rbpj-flox
系統ID
CKOCMP-19664-Rbpj-B6J-VB
遺伝子名
製品ID
S-CKO-18031
遺伝子別名
CBF1, RBP-J, RBPjk, Igkjrb, Rbpsuh, Igkrsbp, RBP-Jkappa, RBP-J kappa
遺伝子別名
C57BL/6JCya
NCBI ID
修正
Conditional knockout
染色体
Chr 5
表現型
アプリケーション
--
さらに
系統詳細
EnsemblトランスクリプトID
ENSMUST00000037618
NCBIトランスクリプトID
NM_009035
ターゲット領域
Exon 4
有効領域の大きさ
~1.8 kb
遺伝子研究の概要
Rbpj, also known as Recombination signal-binding protein for immunoglobulin kappa J region, is a crucial transcriptional regulator. It is the central player in the Notch signaling pathway. In the Notch cascade, it either forms an activator complex with the Notch intracellular domain (NICD) or a repressor complex with corepressors, and this balance is determined by the Notch receptor's activation state. Rbpj is vital for maintaining immune homeostasis and is involved in many biological processes [2,4].
In pancreatic cancer, conditional transgenic mouse models (Ptf1α-CreERT-driven) showed that RBPJ deficiency in adult pancreatic acinar cells doesn't affect their homeostasis but sensitizes them to KRAS-mediated pancreatic intraepithelial neoplasia initiation, promoting fibrotic stroma formation [1].
In epithelial ovarian cancer, deletion of Rbpj in endothelial cells of adult mice reduced monocyte-derived macrophage infiltration into the tumor microenvironment, affecting tumor-associated macrophage (TAM) education and EOC progression [3].
In brain arteriovenous malformation (bAVM) mouse models, deletion of endothelial Rbpj normalized Notch4-induced bAVM, and in an in vivo mouse model of Rbpj-mediated bAVM, Rbpj deficiency disrupted vascular remodeling via abnormal Apelin and Cdc42 activity [5,9].
In uveitis, targeted RBPJ knockdown in rats promoted M2 macrophage polarization through the mtROS-mediated Notch1-Jagged1-Hes1 signaling pathway, ameliorating uveitis [7].
In metabolic dysfunction-associated steatotic liver disease, Rbpj deficiency in mice blunted inflammatory macrophages and monocyte-derived KC differentiation, promoting protective Ly6Clo monocytes [8].
In T-cell fate regulation, targeting RBPJ enhanced functional and epigenetic reprogramming of Tex cells, improving antitumour effects [6].
In conclusion, Rbpj plays essential roles in multiple biological processes mainly through its function in the Notch signaling pathway. Gene knockout and conditional knockout mouse models have significantly contributed to understanding its role in diseases such as pancreatic cancer, epithelial ovarian cancer, bAVM, uveitis, metabolic-associated liver disease, and cancer immunotherapy. These studies provide insights into potential therapeutic strategies targeting Rbpj in these disease areas.
References:
1. Pan, Leiling, Mulaw, Medhanie A, Gout, Johann, Wagner, Martin, Oswald, Franz. 2023. RBPJ Deficiency Sensitizes Pancreatic Acinar Cells to KRAS-Mediated Pancreatic Intraepithelial Neoplasia Initiation. In Cellular and molecular gastroenterology and hepatology, 16, 783-807. doi:10.1016/j.jcmgh.2023.07.013. https://pubmed.ncbi.nlm.nih.gov/37543088/
2. Giaimo, Benedetto Daniele, Gagliani, Ellen K, Kovall, Rhett A, Borggrefe, Tilman. . Transcription Factor RBPJ as a Molecular Switch in Regulating the Notch Response. In Advances in experimental medicine and biology, 1287, 9-30. doi:10.1007/978-3-030-55031-8_2. https://pubmed.ncbi.nlm.nih.gov/33034023/
3. Alsina-Sanchis, Elisenda, Mülfarth, Ronja, Moll, Iris, Fischer, Andreas, Rodriguez-Vita, Juan. . Endothelial RBPJ Is Essential for the Education of Tumor-Associated Macrophages. In Cancer research, 82, 4414-4428. doi:10.1158/0008-5472.CAN-22-0076. https://pubmed.ncbi.nlm.nih.gov/36200806/
4. Chen, Shuaishuai, Zhao, Weibo, Du, Juping, Zhou, Yuanlin, Chen, Shiyong. 2024. The expression of RBPJ and its potential role in rheumatoid arthritis. In BMC genomics, 25, 899. doi:10.1186/s12864-024-10804-2. https://pubmed.ncbi.nlm.nih.gov/39350019/
5. Nielsen, Corinne M, Zhang, Xuetao, Raygor, Kunal, Bollen, Andrew W, Wang, Rong A. 2022. Endothelial Rbpj deletion normalizes Notch4-induced brain arteriovenous malformation in mice. In The Journal of experimental medicine, 220, . doi:10.1084/jem.20211390. https://pubmed.ncbi.nlm.nih.gov/36441145/
6. Zhou, Peipei, Shi, Hao, Huang, Hongling, Pruett-Miller, Shondra M, Chi, Hongbo. 2023. Single-cell CRISPR screens in vivo map T cell fate regulomes in cancer. In Nature, 624, 154-163. doi:10.1038/s41586-023-06733-x. https://pubmed.ncbi.nlm.nih.gov/37968405/
7. Qu, Ruyi, Peng, Yuan, Xu, Shuqin, Bi, Hongsheng, Guo, Dadong. 2024. RBPJ Knockdown Promotes M2 Macrophage Polarization Through Mitochondrial ROS-mediated Notch1-Jagged1-Hes1 Signaling Pathway in Uveitis. In Inflammation, 48, 133-150. doi:10.1007/s10753-024-02053-y. https://pubmed.ncbi.nlm.nih.gov/38761249/
8. Guo, Wei, Li, Ziyi, Anagnostopoulos, Gerasimos, Su, Bing, Ginhoux, Florent. 2024. Notch signaling regulates macrophage-mediated inflammation in metabolic dysfunction-associated steatotic liver disease. In Immunity, 57, 2310-2327.e6. doi:10.1016/j.immuni.2024.08.016. https://pubmed.ncbi.nlm.nih.gov/39317200/
9. Adhicary, Subhodip, Fanelli, Kayleigh, Nakisli, Sera, Pearce, Isaac, Nielsen, Corinne M. 2023. Rbpj Deficiency Disrupts Vascular Remodeling via Abnormal Apelin and Cdc42 (Cell Division Cycle 42) Activity in Brain Arteriovenous Malformation. In Stroke, 54, 1593-1605. doi:10.1161/STROKEAHA.122.041853. https://pubmed.ncbi.nlm.nih.gov/37051908/
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凍結前の精子濃度を測定し、精子の生存能力の判定します。
凍結後の精子では、各バッチから1本の凍結保存された精子を選び出し、体外受精に使用します。
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