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拉曼显微光谱法识别THP-1细胞和外周血单核细胞来源巨噬细胞中的生化激活指纹图谱。

Raman Microspectroscopy Identifies Biochemical Activation Fingerprints in THP-1- and PBMC-Derived Macrophages.

作者信息

Feuerer Nora, Carvajal Berrio Daniel A, Billing Florian, Segan Sören, Weiss Martin, Rothbauer Ulrich, Marzi Julia, Schenke-Layland Katja

机构信息

Institute of Biomedical Engineering, Department for Medical Technologies and Regenerative Medicine, Eberhard Karls University Tübingen, 72076 Tübingen, Germany.

NMI Natural and Medical Sciences Institute at the University of Tübingen, 72770 Reutlingen, Germany.

出版信息

Biomedicines. 2022 Apr 25;10(5):989. doi: 10.3390/biomedicines10050989.

Abstract

(1) The monocytic leukemia cell line THP-1 and primary monocyte-derived macrophages (MDMs) are popular in vitro model systems to study human innate immunity, wound healing, and tissue regeneration. However, both cell types differ significantly in their origin and response to activation stimuli. (2) Resting THP-1 and MDMs were stimulated with lipopolysaccharide (LPS) and interferon γ (IFNγ) and analyzed by Raman microspectroscopy (RM) before and 48 h after activation. Raman data were subsequently analyzed using principal component analysis. (3) We were able to resolve and analyze the spatial distribution and molecular composition of proteins, nucleic acids, and lipids in resting and activated THP-1 and MDMs. Our findings reveal that proinflammatory activation-induced significant spectral alterations at protein and phospholipid levels in THP-1. In MDMs, we identified that nucleic acid and non-membrane-associated intracellular lipid composition were also affected. (4) Our results show that it is crucial to carefully choose the right cell type for an in vitro model as the nature of the cells itself may impact immune cell polarization or activation results. Moreover, we demonstrated that RM is a sensitive tool for investigating cell-specific responses to activation stimuli and monitoring molecular changes in subcellular structures.

摘要

(1) 单核细胞白血病细胞系THP-1和原代单核细胞衍生巨噬细胞(MDM)是研究人类固有免疫、伤口愈合和组织再生的常用体外模型系统。然而,这两种细胞类型在起源和对激活刺激的反应方面存在显著差异。(2) 用脂多糖(LPS)和干扰素γ(IFNγ)刺激静息的THP-1和MDM,并在激活前和激活后48小时通过拉曼光谱(RM)进行分析。随后使用主成分分析对拉曼数据进行分析。(3) 我们能够解析和分析静息及激活状态下的THP-1和MDM中蛋白质、核酸和脂质的空间分布及分子组成。我们的研究结果表明,促炎激活在THP-1的蛋白质和磷脂水平上引起了显著的光谱变化。在MDM中,我们发现核酸和非膜相关的细胞内脂质组成也受到了影响。(4) 我们的结果表明,为体外模型仔细选择合适的细胞类型至关重要,因为细胞本身的性质可能会影响免疫细胞极化或激活结果。此外,我们证明了RM是研究细胞对激活刺激的特异性反应以及监测亚细胞结构分子变化的灵敏工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a64/9139061/eb9234fa0ee0/biomedicines-10-00989-g001.jpg

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