Immunometabolic Properties of Tissue-Resident Alveolar Macrophages Depend on ex vivo Culturing Conditions

IF 2.1 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Olga A. Namakanova, Anastasia S. Yakovleva, Ekaterina O. Gubernatorova, Tamara V. Pukhalskaia, Sergei A. Nedospasov, Marina S. Drutskaya
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引用次数: 0

Abstract

Alveolar macrophages (AMs) comprise the predominant immune cell population in the lungs, maintaining homeostasis and providing the first line of immune defense against various respiratory diseases. Most studies focus on macrophages differentiated from bone marrow precursors in vitro. However, the ontogeny of the tissue-resident macrophages and the lung microenvironment significantly determine their properties and functions, fundamentally distinguishing AMs from the cells derived in vitro. The use of AMs ex vivo, which maximally preserves their original phenotype and proliferative potential, is the most physiological and informative approach for studying various aspects of innate immune responses in lung diseases. Improving methods for their isolation and culturing remains an important task for obtaining relevant data on the functions of these cells. In this study, we evaluated the effect of enzymatic treatment, the most common method for detaching cultured AMs, on their phenotype. It was found that enzymatic treatment led to the decrease in production of GM-CSF and VEGF by the AMs mediators of myeloid cell differentiation and maturation, and angiogenesis, respectively, both in the non-activated state and in response to one of the most common allergens – house dust mite extract (HDM). Enzymatic treatment promoted the formation of a pro-inflammatory phenotype, manifested by the increased production of IL-6, as well as chemokines CCL4 and CCL5, which attract monocytes and lymphocytes to the site of inflammation, along with the trend toward increased expression of the M1-associated genes such as Nos2 and Cd38, in response to HDM. Thus, enzymatic detachment of the tissue-resident AMs promotes M1 polarization, which predetermines a more pronounced response to the allergen in vitro. The presented data highlight disadvantages of the enzymatic treatment of AMs, increasing the risk of artifacts, and affecting reliability of the experimental results.

组织驻留肺泡巨噬细胞的免疫代谢特性取决于体外培养条件
肺泡巨噬细胞(AMs)是肺中主要的免疫细胞群,维持体内平衡,并提供抵抗各种呼吸系统疾病的第一道免疫防线。大多数研究都集中在骨髓前体细胞体外分化的巨噬细胞上。然而,组织内巨噬细胞的个体发生和肺微环境显著地决定了它们的特性和功能,从根本上区分了AMs与体外来源的细胞。体外使用AMs可以最大限度地保留其原始表型和增殖潜力,是研究肺部疾病中先天免疫反应各个方面的最生理和信息丰富的方法。改进它们的分离和培养方法仍然是获得这些细胞功能相关数据的重要任务。在这项研究中,我们评估了酶处理(分离培养的AMs的最常用方法)对其表型的影响。研究发现,在非激活状态和对最常见的过敏原之一——尘螨提取物(HDM)的反应下,酶处理分别导致髓细胞分化、成熟和血管生成的AMs介质中GM-CSF和VEGF的产生减少。酶处理促进了促炎表型的形成,表现为IL-6以及吸引单核细胞和淋巴细胞到炎症部位的趋化因子CCL4和CCL5的产生增加,以及响应HDM的m1相关基因如Nos2和Cd38的表达增加的趋势。因此,组织内的酶解am促进了M1极化,这预先决定了对体外过敏原的更明显的反应。提出的数据突出了酶处理AMs的缺点,增加了伪影的风险,并影响了实验结果的可靠性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Biochemistry (Moscow)
Biochemistry (Moscow) 生物-生化与分子生物学
CiteScore
4.70
自引率
3.60%
发文量
139
审稿时长
2 months
期刊介绍: Biochemistry (Moscow) is the journal that includes research papers in all fields of biochemistry as well as biochemical aspects of molecular biology, bioorganic chemistry, microbiology, immunology, physiology, and biomedical sciences. Coverage also extends to new experimental methods in biochemistry, theoretical contributions of biochemical importance, reviews of contemporary biochemical topics, and mini-reviews (News in Biochemistry).
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