利用膜置换陷阱阵列探测纳升肿瘤共培养物中的 T 细胞活化。

IF 1.5 4区 生物学 Q4 CELL BIOLOGY Integrative Biology Pub Date : 2024-01-23 DOI:10.1093/intbio/zyae014
Michael Yeh, Emanuel Salazar-Cavazos, Anagha Krishnan, Grégoire Altan-Bonnet, Don L DeVoe
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引用次数: 0

摘要

针对癌症的免疫反应本质上是随机的,在一个较大的淋巴细胞集合体中,少量的单个 T 细胞启动分子级联,导致肿瘤细胞毒性。这种肿瘤内变异性的一个潜在来源是免疫细胞对肿瘤细胞的不同反应能力。T细胞和肿瘤细胞的经典微孔共培养不足以可靠地培养和分析探究这种变异性所需的低细胞数,也无法再现在肿瘤中观察到的异质性小域。在这里,我们利用膜置换捕获阵列技术克服了传统微孔板在免疫动力学研究中的局限性。该微流体平台支持在连续灌流的情况下按需形成致密的纳米孔培养物,以反映肿瘤微环境,并实时监测每个纳米孔内 T 细胞的增殖和活化情况。该系统能选择性地排出细胞,通过荧光激活细胞分拣技术进行分析,从而将芯片上观察到的免疫反应变化与芯片外的 T 细胞活化定量联系起来。该技术为探究 T 细胞异质性的分子起源以及确定负责启动和传播肿瘤内免疫级联的特定细胞表型提供了新的可能性。启示盒 T细胞活化的差异性在抗癌免疫反应中起着关键作用。我们需要新的工具来揭示驱动成功的抗肿瘤免疫反应的机制,并支持利用促进有效免疫监视的罕见 T 细胞表型开发新型免疫疗法。为此,我们提出了一种微流体细胞培养平台,该平台能在纳升级孔阵列中探测不同的 T 细胞活化,并结合片外细胞分析,从而能高分辨率地观察肿瘤 / T 细胞共培养物内的可变免疫反应,其中包含的细胞组合比传统孔板研究小很多。
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Probing T-cell activation in nanoliter tumor co-cultures using membrane displacement trap arrays.

Immune responses against cancer are inherently stochastic, with small numbers of individual T cells within a larger ensemble of lymphocytes initiating the molecular cascades that lead to tumor cytotoxicity. A potential source of this intra-tumor variability is the differential ability of immune cells to respond to tumor cells. Classical microwell co-cultures of T cells and tumor cells are inadequate for reliably culturing and analyzing low cell numbers needed to probe this variability, and have failed in recapitulating the heterogeneous small domains observed in tumors. Here we leverage a membrane displacement trap array technology that overcomes limitations of conventional microwell plates for immunodynamic studies. The microfluidic platform supports on-demand formation of dense nanowell cultures under continuous perfusion reflecting the tumor microenvironment, with real-time monitoring of T cell proliferation and activation within each nanowell. The system enables selective ejection of cells for profiling by fluorescence activated cell sorting, allowing observed on-chip variability in immune response to be correlated with off-chip quantification of T cell activation. The technology offers new potential for probing the molecular origins of T cell heterogeneity and identifying specific cell phenotypes responsible for initiating and propagating immune cascades within tumors. Insight Box Variability in T cell activation plays a critical role in the immune response against cancer. New tools are needed to unravel the mechanisms that drive successful anti-tumor immune response, and to support the development of novel immunotherapies utilizing rare T cell phenotypes that promote effective immune surveillance. To this end, we present a microfluidic cell culture platform capable of probing differential T cell activation in an array of nanoliter-scale wells coupled with off-chip cell analysis, enabling a high resolution view of variable immune response within tumor / T cell co-cultures containing cell ensembles orders of magnitude smaller than conventional well plate studies.

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来源期刊
Integrative Biology
Integrative Biology 生物-细胞生物学
CiteScore
4.90
自引率
0.00%
发文量
15
审稿时长
1 months
期刊介绍: Integrative Biology publishes original biological research based on innovative experimental and theoretical methodologies that answer biological questions. The journal is multi- and inter-disciplinary, calling upon expertise and technologies from the physical sciences, engineering, computation, imaging, and mathematics to address critical questions in biological systems. Research using experimental or computational quantitative technologies to characterise biological systems at the molecular, cellular, tissue and population levels is welcomed. Of particular interest are submissions contributing to quantitative understanding of how component properties at one level in the dimensional scale (nano to micro) determine system behaviour at a higher level of complexity. Studies of synthetic systems, whether used to elucidate fundamental principles of biological function or as the basis for novel applications are also of interest.
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