School of Chemical Engineering, College of Engineering, Architecture and Technology, Oklahoma State University, Stillwater, Oklahoma.
Department of Veterinary Pathobiology, Center for Veterinary Health Sciences, Oklahoma State University, Stillwater, Oklahoma.
Tissue Eng Part A. 2019 Nov;25(21-22):1564-1574. doi: 10.1089/ten.TEA.2018.0347. Epub 2019 Aug 9.
Mast cells (MCs) play critical roles in the pathogenesis of IgE- and non-IgE-mediated immune responses, as well as host defense against parasites, bacteria, and viruses. Due to the effect of extracellular matrix components on tissue morphogenesis and cell behavior, utilizing a tissue model that mimics MC microenvironmental conditions has greater relevance for studies. For this work, MCs were developed within a connective tissue-equivalent model and cell function was examined in response to an allergen. MCs are located in proximity to fibroblasts and endothelial cells (ECs) that play a role in MC development and maturity. Accordingly, MC progenitors isolated from human peripheral blood were co-cultured with human primary fibroblasts in a 3D collagen matrix to represent the connective tissue. The matrix was coated with type IV collagen and fibronectin before seeding with primary human ECs, representing the capillary wall. The stem cell-derived cells demonstrated MC characteristics, including typical MC morphology, and the expression of cytoplasmic granules and phenotypic markers. Also, the generated cells released histamine in IgE-mediated reactions, showing typical MC functional phenotype in an immediate-type allergenic response. The created tissue model is applicable to a variety of research studies and allergy testing. Impact Statement Mast cells (MCs) are key effector and immunoregulatory cells in immune disorders; however, their role is not fully understood. Few studies have investigated human MCs in culture, due to the difficulties in isolating large numbers. Our study demonstrates, for the first time, the generation of cells exhibiting MC phenotypic and functional characteristics from hematopoietic stem cells within a connective tissue-equivalent model with ancillary cells. Utilizing the 3D matrix-embedded cells can advance our understanding of MC biological profile and immunoregulatory roles. The tissue model can also be used for studying the mechanism of allergic diseases and other inflammatory disorders.
肥大细胞(MCs)在 IgE 和非 IgE 介导的免疫反应的发病机制中以及宿主对寄生虫、细菌和病毒的防御中发挥关键作用。由于细胞外基质成分对组织形态发生和细胞行为的影响,利用模拟 MC 微环境条件的组织模型更有助于研究。在这项工作中,MC 是在结缔组织等效模型中发育的,并检测了它们对过敏原的反应。MC 位于靠近成纤维细胞和内皮细胞(ECs)的位置,这些细胞在 MC 的发育和成熟中发挥作用。因此,从人外周血中分离出的 MC 祖细胞与原代人成纤维细胞在 3D 胶原基质中共培养,以代表结缔组织。基质在接种原代人 ECs 之前用 IV 型胶原和纤连蛋白包被,代表毛细血管壁。由干细胞衍生的细胞表现出 MC 的特征,包括典型的 MC 形态以及细胞质颗粒和表型标志物的表达。此外,生成的细胞在 IgE 介导的反应中释放组胺,显示出在即刻型变应原反应中的典型 MC 功能表型。所创建的组织模型适用于各种研究和过敏测试。
影响说明肥大细胞(MCs)是免疫紊乱中的关键效应和免疫调节细胞;然而,其作用尚未完全了解。由于难以分离大量细胞,因此很少有研究在培养中研究人类 MC。我们的研究首次证明了在具有辅助细胞的结缔组织等效模型中,从造血干细胞生成表现出 MC 表型和功能特征的细胞。利用 3D 基质嵌入细胞可以促进我们对 MC 生物学特征和免疫调节作用的理解。该组织模型还可用于研究过敏疾病和其他炎症性疾病的发病机制。