Division of Chemical, Systems, and Synthetic Biology, Department of Integrative Biomedical Sciences, Institute of Infectious Disease & Molecular Medicine, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.
Radboud Institute for Molecular Life Sciences (RIMLS), Radboud University Medical Center, Nijmegen, Netherlands.
Front Immunol. 2021 May 11;12:662565. doi: 10.3389/fimmu.2021.662565. eCollection 2021.
Mammals face and overcome an onslaught of endogenous and exogenous challenges in order to survive. Typical immune cells and barrier cells, such as epithelia, must respond rapidly and effectively to encountered pathogens and aberrant cells to prevent invasion and eliminate pathogenic species before they become overgrown and cause harm. On the other hand, inappropriate initiation and failed termination of immune cell effector function in the absence of pathogens or aberrant tissue gives rise to a number of chronic, auto-immune, and neoplastic diseases. Therefore, the fine control of immune effector functions to provide for a rapid, robust response to challenge is essential. Importantly, immune cells are heterogeneous due to various factors relating to cytokine exposure and cell-cell interaction. For instance, tissue-resident macrophages and T cells are phenotypically, transcriptionally, and functionally distinct from their circulating counterparts. Indeed, even the same cell types in the same environment show distinct transcription patterns at the single cell level due to cellular noise, despite being robust in concert. Additionally, immune cells must remain quiescent in a naive state to avoid autoimmunity or chronic inflammatory states but must respond robustly upon activation regardless of their microenvironment or cellular noise. In recent years, accruing evidence from next-generation sequencing, chromatin capture techniques, and high-resolution imaging has shown that local- and long-range genome architecture plays an important role in coordinating rapid and robust transcriptional responses. Here, we discuss the local- and long-range genome architecture of immune cells and the resultant changes upon pathogen or antigen exposure. Furthermore, we argue that genome structures contribute functionally to rapid and robust responses under noisy and distinct cellular environments and propose a model to explain this phenomenon.
哺乳动物为了生存,需要面对并克服内源性和外源性的挑战。典型的免疫细胞和屏障细胞,如上皮细胞,必须迅速有效地对遇到的病原体和异常细胞作出反应,以防止它们过度生长并造成伤害。另一方面,如果没有病原体或异常组织,免疫细胞效应功能的不当启动和失效终止会导致许多慢性、自身免疫和肿瘤疾病。因此,精细控制免疫效应功能以提供对挑战的快速、强大反应是至关重要的。重要的是,免疫细胞由于与细胞因子暴露和细胞-细胞相互作用有关的各种因素而表现出异质性。例如,组织驻留的巨噬细胞和 T 细胞在表型、转录和功能上与它们的循环对应物不同。事实上,即使是同一环境中的相同细胞类型,由于细胞噪声,即使在协调一致时也表现出明显的转录模式,尽管在单细胞水平上是稳健的。此外,免疫细胞必须保持静息状态以避免自身免疫或慢性炎症状态,但无论其微环境或细胞噪声如何,都必须在激活时做出强烈反应。近年来,下一代测序、染色质捕获技术和高分辨率成像的累积证据表明,局部和长程基因组结构在协调快速和强大的转录反应中起着重要作用。在这里,我们讨论了免疫细胞的局部和长程基因组结构以及病原体或抗原暴露后的变化。此外,我们认为基因组结构有助于在嘈杂和不同的细胞环境下快速而强大的反应,并提出了一个解释这一现象的模型。