PDL2/TCR Activator/CHO
CBP74065
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產(chǎn)品描述
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| I. Background | |
| Programmed Cell Death Protein 1 (PD-1)，一種在激活的 T 細(xì)胞上表達(dá)的受體，與其配 體 PD-L1 和 PD-L2 結(jié)合，負(fù)向調(diào)節(jié)免疫反應(yīng)。 PD-1 配體存在于大多數(shù)癌癥中，PD-1:PD- L1/2 相互作用會(huì)抑制 T 細(xì)胞活性，并使癌細(xì)胞逃避免疫監(jiān)視。 PD1/PDL1 信號(hào)轉(zhuǎn)導(dǎo)通路是 腫瘤免疫抑制的重要組成部分，可以抑制 T 淋巴細(xì)胞的興奮，增強(qiáng)腫瘤細(xì)胞的免疫耐受， 從而實(shí)現(xiàn)腫瘤免疫逃逸。PD1 與 PDL1 結(jié)合可以減弱 T 細(xì)胞介導(dǎo)的免疫監(jiān)視，導(dǎo)致免疫反 應(yīng)缺失，甚至導(dǎo)致 T 細(xì)胞凋亡。PD1/PDL1 抑制劑可解除抗腫瘤 T 細(xì)胞的免疫抑制，從而 導(dǎo)致 T 細(xì)胞增殖并滲透到腫瘤微環(huán)境中并誘導(dǎo)抗腫瘤反應(yīng)。PD-1:PD-L1/2 通路還參與調(diào)節(jié) 自身免疫反應(yīng)，使這些蛋白質(zhì)成為多種癌癥以及多發(fā)性硬化癥、關(guān)節(jié)炎、狼瘡和 I 型糖尿 病的有希望的治療靶點(diǎn)。酪氨酸磷酸酶 SHP2 是 T 細(xì)胞功能的關(guān)鍵調(diào)節(jié)因子，它介導(dǎo) TCR 下游的激活信號(hào)以及 PD-1 下游的抑制信號(hào)。 | |
| II. Description | |
PDL2 TCR Activator CHO 細(xì)胞作為 PD1 NFAT-Luc Jurkat 細(xì)胞的靶細(xì)胞，很好的模擬了 體內(nèi) PD1&PDL2 的信號(hào)轉(zhuǎn)導(dǎo)過程，原理見下圖所示。 Figure 1. PDL2 TCR Activator CHO 細(xì)胞模型原理圖
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| III. Introduction | |
| Host Cell: | CHO-K1 |
| Expressed gene: | PDL2 |
| Stability: | 32 passages (in-house test, that not means the cell line will be instable beyond the passages we tested.) |
| Synonym(s): | Programmed Cell Death 2 Ligand 2, PDL2, PD-L2, CD273, PDCDL1G2, B7-DC |
| Freeze Medium: | 90% FBS+10% DMSO |
| Culture Medium: | F12K+10%FBS+2ug/ml puromycin+500ug/ml hygromycin |
| Mycoplasma Testing: | Negative |
| Storage: | Liquid nitrogen |
| Application(s): | Functional(Report Gene) Assay |
| IV. Description of Host Cell Line | |
| Organism: | Cricetulus griseus, hamster, Chinese |
| Tissue: | Ovary |
| Disease: | Hamster Chinese ovary |
| Morphology: | Epitheloid cell |
| Growth Properties: | Adherent |
| Ⅴ. Representative Data | |
Figure 2.Recombinant PDL2/TCR Activator/CHO constitutively expressing PDL2.
Figure 3. Dose Responese of anti-PD1 neutralizing antibody in PD1 NFAT-Luc Jurkat (C16) with PDL2 TCR Activator CHO(C1).
