Clec4a3-KO Mouse
一般名
Clec4a3-KO
製品ID
S-KO-17836
背景情報
C57BL/6JCya
系統ID
KOCMP-73149-Clec4a3-B6J-VB
状況
このマウス系統を論文で使用する場合は、「Clec4a3-KO Mouse(カタログ番号S-KO-17836)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
Clec4a3-KO
系統ID
KOCMP-73149-Clec4a3-B6J-VB
遺伝子名
製品ID
S-KO-17836
遺伝子別名
Dcir3, 3110037K17Rik
遺伝子別名
C57BL/6JCya
NCBI ID
修正
Conventional knockout
染色体
Chr 6
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
ENSMUST00000088468
NCBIトランスクリプトID
NM_153197
ターゲット領域
Exon 4
有効領域の大きさ
~1.4 kb
遺伝子研究の概要
Clec4a3, also known as Dendritic cell inhibitory receptor 3 (DCIR3), is a C-type lectin receptor belonging to the mouse dendritic cell immunoreceptor (DCIR) family. C-type lectin receptors are important for initiating and shaping immune responses. Clec4a3 is involved in the regulation of lymphocyte trafficking, motor neuron survival, and may play a role in innate immunity and antigen-presenting processes [3,5,6].
In a study on pulmonary arterial hypertension, Clec4a3 was identified as one of the hub genes associated with the dysregulated B-cell receptor signaling pathway and humoral immune response [2]. In rat models of ventral root avulsion, genetic variability in the Aplec cluster containing Clec4a3 regulated motor neuron survival and T-cell infiltration into the spinal cord [3]. In microglial transcriptome studies of neonatal and adult mice after spinal cord injury, Clec4a3 was selected as one of the hub genes for further validation, suggesting its potential role in injury-related processes [4]. In a study on a novel exosome-like nanosystem for liver cancer, Clec4a3 expression was downregulated in M2 macrophages after treatment, which may be related to the regulation of the tumor immune microenvironment [1].
In conclusion, Clec4a3 plays important roles in immune-related processes, including lymphocyte trafficking, humoral immunity, and microglial-related responses in injury, as well as in the regulation of the tumor immune microenvironment. Studies on Clec4a3 using animal models have provided insights into its functions in various disease-related conditions such as pulmonary arterial hypertension, spinal cord injury, and liver cancer.
References:
1. Chen, Yichi, Li, Xudong, Shang, Haitao, Wu, Bolin, Cheng, Wen. 2024. Mechanism exploration of synergistic photo-immunotherapy strategy based on a novel exosome-like nanosystem for remodeling the immune microenvironment of HCC. In Nano convergence, 11, 31. doi:10.1186/s40580-024-00441-6. https://pubmed.ncbi.nlm.nih.gov/39141072/
2. Chen, Yuanrong, Wu, Chaoling, Wang, Xiaoping, Zhong, Yiming, Xiao, Genfa. 2022. Weighted gene co-expression network analysis identifies dysregulated B-cell receptor signaling pathway and novel genes in pulmonary arterial hypertension. In Frontiers in cardiovascular medicine, 9, 909399. doi:10.3389/fcvm.2022.909399. https://pubmed.ncbi.nlm.nih.gov/36277750/
3. Lindblom, Rickard P F, Aeinehband, Shahin, Parsa, Roham, Diez, Margarita, Piehl, Fredrik. 2013. Genetic variability in the rat Aplec C-type lectin gene cluster regulates lymphocyte trafficking and motor neuron survival after traumatic nerve root injury. In Journal of neuroinflammation, 10, 60. doi:10.1186/1742-2094-10-60. https://pubmed.ncbi.nlm.nih.gov/23656637/
4. Jiang, Qi, Xue, Shiyuan, Pan, Xiaojing, Hu, Die, Fu, Haitao. 2025. Differential changes in the microglial transcriptome between neonatal and adult mice after spinal cord injury. In Scientific reports, 15, 13708. doi:10.1038/s41598-025-98429-7. https://pubmed.ncbi.nlm.nih.gov/40258965/
5. Hey, Ying-Ying, O'Neill, Helen C. 2016. Antigen Presenting Properties of a Myeloid Dendritic-Like Cell in Murine Spleen. In PloS one, 11, e0162358. doi:10.1371/journal.pone.0162358. https://pubmed.ncbi.nlm.nih.gov/27654936/
6. Nesterovitch, Andrew B, Arbieva, Zarema, Toth, Daniel M, Tharp, Michael D, Glant, Tibor T. 2016. A differential gene expression study: Ptpn6 (SHP-1)-insufficiency leads to neutrophilic dermatosis-like disease (NDLD) in mice. In Journal of dermatological science, 83, 17-25. doi:10.1016/j.jdermsci.2016.03.005. https://pubmed.ncbi.nlm.nih.gov/27020408/
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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。
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グローバル由来:
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