C5aR1/CHO
CBP71374
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| I. Background | |
| 補體 C5a 是由補體系統(tǒng)經 C5 轉化酶裂解 C5 產生的強效炎癥介質，作為核心過敏毒素 通過結合受體 C5aR1/C5aR2 驅動中性粒細胞趨化、氧化爆發(fā)及炎性因子（IL-6/TNF-α）釋 放，在膿毒癥中誘發(fā)“細胞因子風暴”，在自身免疫?。ㄈ珙愶L濕關節(jié)炎）中促進組織侵 蝕，在腫瘤微環(huán)境募集髓系抑制細胞（MDSC）介導免疫逃逸。 C5aR1（CD88）是補體過敏毒素 C5a 的高親和力 GPCR，主要表達于髓系細胞（中性 粒細胞、單核細胞、肥大細胞），通過激活 Gi/Gq 蛋白-PI3K/MAPK 通路驅動炎癥級聯(lián)反應。 |
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| II. Description | |
C5aR1 CHO 藥靶模型很好的模擬了體內 C5aR1 的信號轉導過程，原理見下圖所示。 Figure 1. C5aR1 CHO 細胞模型原理圖 |
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| III. Introduction | |
| Host Cell: |
CHO |
| Stability: | 20 passages (in-house test, that not means the cell line will be instable beyond the passages we tested.) |
| Freeze Medium: | 90% FBS+10% DMSO |
| Culture Medium: | F12K+10%FBS+5ug/ml puromycin |
| Mycoplasma Status: | Negative |
| Storage: | Liquid nitrogen immediately upon delivery |
| Application(s): |
Functional assay for C5aR1 |
| Transducer: | Gi |
| IV. Description of Host Cell Line | |
| Organism: | Hamster |
| Tissue: | Ovary |
| Morphology: | Epithelial |
| Growth Properties: | Adherent |
| V. Representative Data | |
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Figure 2. Recombinant C5aR1/CHO constitutively expressing C5aR1. |
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Figure 3. HTRF cAMP Assay With C5aR1 CHO Cell (C7). |
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