Apoh-KO Mouse
一般名
Apoh-KO
製品ID
S-KO-01102
背景情報
C57BL/6NCya
系統ID
KOCMP-11818-Apoh-B6N-VA
状況
このマウス系統を論文で使用する場合は、「Apoh-KO Mouse(カタログ番号S-KO-01102)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
Apoh-KO
系統ID
KOCMP-11818-Apoh-B6N-VA
遺伝子名
製品ID
S-KO-01102
遺伝子別名
B2GPI, beta2-GPI, beta-2-GPI
遺伝子別名
C57BL/6NCya
NCBI ID
修正
Conventional knockout
染色体
Chr 11
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
ENSMUST00000000049
NCBIトランスクリプトID
NM_013475
ターゲット領域
Exon 2~3
有効領域の大きさ
~1.6 kb
遺伝子研究の概要
Apoh, also known as apolipoprotein H, is involved in lipid metabolism, regulating triglycerides, and is a component of HDL. It can bind free fatty acids, regulate the activity of many proteins involved in HDL metabolism, inhibit lipid transfer, and control the endogenous coagulation cascade. It also plays roles in complement and coagulation pathways [5,7].
In the context of antiphospholipid syndrome (APS), exosome-contained Apoh is associated with this disease. APS-exos, which contain Apoh, can cause APS-like birth outcomes, inhibit the migration and tube formation of human umbilical vein endothelial cells (HUVECs), and impair vascular development, leading to pregnancy complications. APOH-exos may play a role through the phospho-extracellular signal-regulated kinase pathway [1]. In addition, polymorphisms in the APOH gene are associated with susceptibility to recurrent pregnancy loss in women with APS [2].
In type 2 diabetic patients, Apoh plasma levels are significantly associated with triglycerides, components of triglyceride-rich lipoproteins, and RBP4 levels. Apoh is higher in type 2 diabetic patients with metabolic syndrome (MS) and with macrovascular disease, and the enhanced levels are due to increased liver synthesis [3]. In diabetic kidney disease (DKD) mice, the mRNA expression level of Apoh is declined [4]. Fructus arctii, a traditional medicinal plant, alleviates diabetic nephropathy progression by modulating cell proliferation and renal fibrosis via the Apoh/PPAR-γ pathway. Apoh overexpression suppresses high-glucose-induced cell proliferation and alleviates fibrosis in relevant cells [6].
In influenza-infected patients, low plasma levels of ApoH are associated with a worse prognosis, and adequate plasma levels of ApoH are protective against severe influenza and respiratory failure [7].
In summary, Apoh is crucial in lipid metabolism, HDL-related functions, and complement and coagulation pathways. Studies using models (such as mouse models in APS-related pregnancy complications, DKD, and diabetic nephropathy) have revealed its roles in various disease conditions, including APS, type 2 diabetes-related complications, DKD, and influenza-associated prognosis. These findings provide insights into the biological functions of Apoh and potential therapeutic targets for related diseases.
References:
1. Tan, Yuan, Bian, Yiding, Song, Yunfeng, Zhang, Qinhua, Wan, Xiaoping. 2021. Exosome-Contained APOH Associated With Antiphospholipid Syndrome. In Frontiers in immunology, 12, 604222. doi:10.3389/fimmu.2021.604222. https://pubmed.ncbi.nlm.nih.gov/34040601/
2. Deng, Xujing, Sang, Qing, Zhang, Ruixiu, Mu, Jian, Bao, Shihua. 2023. The association of APOH and NCF1 polymorphisms on susceptibility to recurrent pregnancy loss in women with antiphospholipid syndrome. In Journal of assisted reproduction and genetics, 40, 1703-1712. doi:10.1007/s10815-023-02829-5. https://pubmed.ncbi.nlm.nih.gov/37243946/
3. Castro, Antoni, Lázaro, Iolanda, Selva, David M, Simó, Rafael, Masana, Lluís. 2009. APOH is increased in the plasma and liver of type 2 diabetic patients with metabolic syndrome. In Atherosclerosis, 209, 201-5. doi:10.1016/j.atherosclerosis.2009.09.072. https://pubmed.ncbi.nlm.nih.gov/19878946/
4. Zhao, Jing, He, Kaiying, Du, Hongxuan, Zhou, Xiaochun, Wang, Jianqin. 2022. Bioinformatics prediction and experimental verification of key biomarkers for diabetic kidney disease based on transcriptome sequencing in mice. In PeerJ, 10, e13932. doi:10.7717/peerj.13932. https://pubmed.ncbi.nlm.nih.gov/36157062/
5. Deng, Siying, Xu, Yangkai, Zheng, Lemin. . HDL Structure. In Advances in experimental medicine and biology, 1377, 1-11. doi:10.1007/978-981-19-1592-5_1. https://pubmed.ncbi.nlm.nih.gov/35575917/
6. Zhang, Na, Chen, Anhui, Dong, Yuwei, Dou, Deqiang. 2025. Fructus arctii mitigates diabetic nephropathy via the Apoh/PPAR-γ pathway. In Molecular immunology, 181, 18-28. doi:10.1016/j.molimm.2025.02.017. https://pubmed.ncbi.nlm.nih.gov/40056629/
7. Garcinuño, Sara, Lalueza, Antonio, Gil-Etayo, Francisco Javier, Serrano, Antonio, Serrano, Manuel. 2024. Immune dysregulation is an important factor in the underlying complications in Influenza infection. ApoH, IL-8 and IL-15 as markers of prognosis. In Frontiers in immunology, 15, 1443096. doi:10.3389/fimmu.2024.1443096. https://pubmed.ncbi.nlm.nih.gov/39176097/
品質管理基準
精子検査
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。
環境基準:
SPF対応地域:
グローバル由来:
Cyagenお問い合わせ
カスタムの動物モデルに関するご相談は、下記のフォームにご記入いただき、ご連絡いただくか見積もりをご依頼ください。
Cyagenはお客様のプライバシーを大変重視しています。当社の最新の製品や情報をお届けしたいと思っています。お客様の設定をご確認ください。
これらの配信はいつでも解除できます。配信停止方法およびデータ保護の詳細は プライバシーポリシー をご確認ください。
以下のボタンをクリックすることで、このフォームにご入力いただいた個人情報をCyagenが保存・処理し、ご要望のコンテンツを提供することに同意されたことになります。
