Co-culture of multiple myeloma cell lines and bone marrow mesenchymal stem cells in a 3D microgel environment

IF 6 2区 医学 Q2 MATERIALS SCIENCE, BIOMATERIALS Materials Science & Engineering C-Materials for Biological Applications Pub Date : 2025-07-01 Epub Date: 2025-02-28 DOI:10.1016/j.bioadv.2025.214243
M. Inmaculada García-Briega , Júlia Plá-Salom , Sandra Clara-Trujillo , Laia Tolosa , Lourdes Cordón , Amparo Sempere , José Luís Gómez Ribelles
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Abstract

This study reproduces the complex relationships between tumour plasma cells and their bone marrow microenvironment in multiple myeloma in vitro. These relationships are established both with other cells and with the extracellular matrix and are key factors in tumour progression, generating resistance to antitumour drugs in the cellular and non-cellular environments. This paper proposes a 3D microenvironment model designed to capture the main components of the multiple myeloma tumour microenvironment. Multiple myeloma cells (MMCs) were dispersed in a microgel medium formed by gel-textured microspheres. The proteins and polysaccharides considered important in the interaction of the MMCs with their non-cellular environment were successfully grafted onto the surface of the microspheres, while human mesenchymal stem cells (MSCs) were cultured in a pellet with non-functionalised microspheres. The MSCs pellet was placed in the well plate together with the microgel and the MMCs and orbitally shaken to maintain them in suspension. The viability, cell cycle and proliferation of the RPMI8226, MM1S and U266 multiple myeloma cell lines and the direct adhesion of MMCs to the MSC pellet were quantified. The results revealed that all three cell lines are able to grow satisfactorily. In addition, the normal behaviour of the MMCs is not modified in any of the culture conditions studied.

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多发性骨髓瘤细胞系与骨髓间充质干细胞在三维微凝胶环境中的共培养
本研究在体外再现了多发性骨髓瘤肿瘤浆细胞与其骨髓微环境之间的复杂关系。这些关系既与其他细胞建立,也与细胞外基质建立,是肿瘤进展的关键因素,在细胞和非细胞环境中产生抗肿瘤药物耐药性。本文提出了一个三维微环境模型,旨在捕捉多发性骨髓瘤肿瘤微环境的主要组成部分。多发性骨髓瘤细胞(MMCs)分散在凝胶微球形成的微凝胶培养基中。在mmc与其非细胞环境相互作用中被认为是重要的蛋白质和多糖被成功地移植到微球表面,而人间充质干细胞(MSCs)被培养在具有非功能化微球的颗粒中。将MSCs颗粒与微凝胶和MSCs一起置于孔板中,并进行轨道振荡以保持其悬浮状态。定量测定RPMI8226、MM1S和U266多发性骨髓瘤细胞系的活力、细胞周期和增殖以及mmc与MSC颗粒的直接粘附。结果表明,这三种细胞系都能令人满意地生长。此外,在研究的任何培养条件下,MMCs的正常行为都没有改变。
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来源期刊
CiteScore
17.80
自引率
0.00%
发文量
501
审稿时长
27 days
期刊介绍: Biomaterials Advances, previously known as Materials Science and Engineering: C-Materials for Biological Applications (P-ISSN: 0928-4931, E-ISSN: 1873-0191). Includes topics at the interface of the biomedical sciences and materials engineering. These topics include: • Bioinspired and biomimetic materials for medical applications • Materials of biological origin for medical applications • Materials for "active" medical applications • Self-assembling and self-healing materials for medical applications • "Smart" (i.e., stimulus-response) materials for medical applications • Ceramic, metallic, polymeric, and composite materials for medical applications • Materials for in vivo sensing • Materials for in vivo imaging • Materials for delivery of pharmacologic agents and vaccines • Novel approaches for characterizing and modeling materials for medical applications Manuscripts on biological topics without a materials science component, or manuscripts on materials science without biological applications, will not be considered for publication in Materials Science and Engineering C. New submissions are first assessed for language, scope and originality (plagiarism check) and can be desk rejected before review if they need English language improvements, are out of scope or present excessive duplication with published sources. Biomaterials Advances sits within Elsevier''s biomaterials science portfolio alongside Biomaterials, Materials Today Bio and Biomaterials and Biosystems. As part of the broader Materials Today family, Biomaterials Advances offers authors rigorous peer review, rapid decisions, and high visibility. We look forward to receiving your submissions!
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