Ccl5-KO Mouse
一般名
Ccl5-KO
製品ID
S-KO-04232
背景情報
C57BL/6JCya
系統ID
KOCMP-20304-Ccl5-B6J-VB
状況
このマウス系統を論文で使用する場合は、「Ccl5-KO Mouse(カタログ番号S-KO-04232)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
Ccl5-KO
系統ID
KOCMP-20304-Ccl5-B6J-VB
遺伝子名
製品ID
S-KO-04232
遺伝子別名
SISd, Scya5, RANTES, TCP228, MuRantes
遺伝子別名
C57BL/6JCya
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
ENSMUST00000035938
NCBIトランスクリプトID
NM_013653
ターゲット領域
Exon 2
有効領域の大きさ
~0.1 kb
遺伝子研究の概要
Ccl5, also known as RANTES (regulated on activation, normal T cell expressed and secreted), is a proinflammatory CC subfamily chemokine synthesized by T lymphocytes. It plays a role in immune regulation, being involved in processes such as cell migration and recruitment of immune cells. It may participate in multiple pathways related to inflammation and cancer-related events [3].
In various disease conditions, Ccl5 has been shown to have significant impacts. In pancreatic cancer, scRNA-seq analysis found CCL5-SDC1/4 receptor-ligand interactions between T cells and tumor cells, and CCL5 promoted tumor cell migration in vitro [1]. In glioma, CCL5 from glioma-associated microglia/macrophages regulated glioma migration and invasion via calcium-dependent matrix metalloproteinase 2 [2]. In chordoma, chordoma-secreted CCL5 promoted malignancy progression, macrophage recruitment, and M2 polarization, and CCL5 knockdown inhibited chordoma malignant progression [5]. In renal cancer, CCL5 promoted the epithelial-mesenchymal transition of circulating tumor cells through smad2/3, enhancing the malignant phenotype and facilitating lung metastasis [6]. However, in osteoarthritis, mice lacking CCL5 or CCR5 were not protected against OA, indicating that CCL5/CCR5 may not mediate monocyte recruitment, inflammation, and cartilage destruction in this disease [4].
In conclusion, Ccl5 is a crucial chemokine involved in immune-related processes and has a significant impact on the progression of several cancers, such as pancreatic, glioma, chordoma, and renal cancer. Its role in diseases like osteoarthritis seems to be different. The study of Ccl5, especially through gene knockout models in mouse studies, helps to understand its function in specific biological processes and disease conditions, providing potential therapeutic targets for these diseases.
References:
1. Chen, Kai, Wang, Yazhou, Hou, Yuting, Tian, Xiaodong, Yang, Yinmo. 2022. Single cell RNA-seq reveals the CCL5/SDC1 receptor-ligand interaction between T cells and tumor cells in pancreatic cancer. In Cancer letters, 545, 215834. doi:10.1016/j.canlet.2022.215834. https://pubmed.ncbi.nlm.nih.gov/35917973/
2. Yu-Ju Wu, Caren, Chen, Chia-Hua, Lin, Chun-Yen, Fang, Jia-You, Chen, Pin-Yuan. . CCL5 of glioma-associated microglia/macrophages regulates glioma migration and invasion via calcium-dependent matrix metalloproteinase 2. In Neuro-oncology, 22, 253-266. doi:10.1093/neuonc/noz189. https://pubmed.ncbi.nlm.nih.gov/31593589/
3. Barczak, Katarzyna, Droździk, Agnieszka, Bosiacki, Mateusz, Uriciuc, Willi Andrei, Baranowska-Bosiacka, Irena. 2023. CCL5's Role in Periodontal Disease: A Narrative Review. In International journal of molecular sciences, 24, . doi:10.3390/ijms242417332. https://pubmed.ncbi.nlm.nih.gov/38139161/
4. Raghu, Harini, Lepus, Christin M, Wang, Qian, Sokolove, Jeremy B, Robinson, William H. 2016. CCL2/CCR2, but not CCL5/CCR5, mediates monocyte recruitment, inflammation and cartilage destruction in osteoarthritis. In Annals of the rheumatic diseases, 76, 914-922. doi:10.1136/annrheumdis-2016-210426. https://pubmed.ncbi.nlm.nih.gov/27965260/
5. Xu, Jiuhui, Shi, Qianyu, Lou, Jingbing, Ren, Tingting, Tang, Xiaodong. . Chordoma recruits and polarizes tumor-associated macrophages via secreting CCL5 to promote malignant progression. In Journal for immunotherapy of cancer, 11, . doi:10.1136/jitc-2023-006808. https://pubmed.ncbi.nlm.nih.gov/37185233/
6. Guan, Yibing, Liu, Xueyi, Tian, Juanhua, Gao, Mei, Chong, Tie. 2024. CCL5 promotes the epithelial-mesenchymal transition of circulating tumor cells in renal cancer. In Journal of translational medicine, 22, 817. doi:10.1186/s12967-024-05297-2. https://pubmed.ncbi.nlm.nih.gov/39227943/
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