RNF43 p.G659fs 通过 PI3K/AKT/mTOR 信号通路和 HLA-E 上调导致 MSI-high 结直肠癌中 NK 细胞功能障碍
RNF43 p.G659fs leads to natural killer cell dysfunction in MSI-high colorectal cancer through PI3K/AKT/mTOR signaling and HLA-E up-regulation.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:A Thermo-responsive collapse system for controlling heterogeneous cell localization, ratio and interaction for three-dimensional solid tumor modeling.
A Thermo-responsive collapse system for controlling heterogeneous cell localization, ratio and interaction for three-dimensional solid tumor modeling.
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利用工程化细胞毒性效应细胞的癌症免疫治疗已显示出巨大潜力。然而,现有体外模型的空间复杂性有限,这对试图在三维实体肿瘤样环境中验证现有效应细胞介导细胞毒性方法的机制研究构成了挑战。为了获得更多的实验控制,我们开发了一种利用形成温度响应性水凝胶的智能聚合物构建三维(3D)培养模型的方法。通过将细胞包埋在这些水凝胶中,我们构建了3D模型,可按需以指定比例组织多个细胞群体,并利用水凝胶的相变温和地定位它们。这些系统适用于低分辨率和高分辨率成像以评估细胞间相互作用,也适用于解离以进行单细胞分析。
我们将这种方法称为“层热塌缩”(TheCOS),并展示了其在按需创建层状和球状复杂细胞组装体中的应用。作为一项应用,我们利用TheCOS评估了自然杀伤(NK)细胞裂解颗粒脱颗粒方向性的影响。通过抑制动力蛋白来阻断裂解颗粒的汇聚和极化,已被证明可在单细胞悬液中诱导旁观者杀伤。利用TheCOS,我们表明由动力蛋白抑制诱导的裂解颗粒分散可在3D中维持,并导致多向杀伤,包括对非触发旁观者细胞的杀伤。通过对TheCOS实验进行成像,我们能够在模拟实体肿瘤环境中绘制与多向脱颗粒相关的“杀伤区”。TheCOS应允许测试改变细胞毒性机制的方法,以及生成广泛的人类肿瘤微环境,以加速肿瘤免疫治疗。
Cancer immunotherapy using engineered cytotoxic effector cells has demonstrated significant potential. The limited spatial complexity of existing in vitro models, however, poses a challenge to mechanistic studies attempting to approve existing approaches of effector cell-mediated cytotoxicity within a three-dimensional, solid tumor-like environment. To gain additional experimental control, we developed an approach for constructing three-dimensional (3D) culture models using smart polymers that form temperature responsive hydrogels.
By embedding cells in these hydrogels, we constructed 3D models to organize multiple cell populations at specified ratios on-demand and gently position them by exploiting the hydrogel phase transition. These systems were amenable to imaging at low- and high-resolution to evaluate cell-to-cell interactions, as well as to dissociation to allow for single cell analyses.
We have called this approach "thermal collapse of strata" (TheCOS) and demonstrated its use in creating complex cell assemblies on demand in both layers and spheroids. As an application, we utilized TheCOS to evaluate the impact of directionality of degranulation of natural killer (NK) cell lytic granules. Blocking lytic granule convergence and polarization by inhibiting dynein has been shown to induce bystander killing in single cell suspensions.
Using TheCOS we showed that lytic granule dispersion induced by dynein inhibition can be sustained in 3D and results in a multi-directional killing including that of non-triggering bystander cells. By imaging TheCOS experiments, we were able to map a "kill zone" associated with multi-directional degranulation in simulated solid tumor environments.
TheCOS should allow for the testing of approaches to alter the mechanics of cytotoxicity as well as to generate a wide-array of human tumor microenvironments to assist in the acceleration of tumor immunotherapy.
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