High-Throughput Label-Free Continuous Quantification of Muscle Stem Cell Proliferation and Myogenic Differentiation.

IF 4.2 3区 医学 Q2 CELL & TISSUE ENGINEERING
Stig Skrivergaard, Martin Krøyer Rasmussen, Margrethe Therkildsen, Jette Feveile Young
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引用次数: 0

Abstract

Background: Quantifying muscle satellite cell proliferation and differentiation is crucial for applications in muscle regeneration, disease modeling, and cultivated meat research. Traditional fluorescence-based assays, while sensitive, are labor-intensive, endpoint-restricted, and disruptive to myotube integrity.

Methods: In this study, we present a novel high-contrast brightfield (HCBF) imaging technique for high-throughput, label-free assessment of both satellite cell proliferation and myogenic differentiation. Using the BioTek Cytation 5 automated imager and Gen5 software (Agilent Technologies), we optimized imaging parameters to achieve continuous, highly time-resolved quantification in standard 96- and 384-well formats without any additional reagents or cell manipulation needed.

Results: Our approach enabled detailed kinetic profiling of satellite cell behavior, revealing myotube formation dynamics, species-specific media responses, optimal seeding conditions and the influence of mechanical factors on differentiation. We also demonstrated that serum-free media formulations could support efficient myotube formation in both bovine and porcine satellite cells, while having very different myotube kinetics and morphology than serum-containing samples. Furthermore, we highlighted the high degree of well-to-well variation and the sporadic formation and detachment of myotubes in culture, and the interesting phenomena of a second wave of myotubes being formed following detachment in serum-containing samples. Additionally, the 384-well format enabled a label-free screening method to assess clonal myogenicity of isolated satellite cells.

Conclusion: By eliminating the need for genetic labeling, invasive staining or specialized consumables, our high-throughput HCBF methodology advances myogenic research, offering new opportunities for efficient screening and highly detailed kinetic data acquisition for serum-free media development, drug discovery and pathophysiological testing for both cultivated meat and musculoskeletal research.

肌肉干细胞增殖和成肌分化的高通量无标记连续定量。
背景:量化肌肉卫星细胞的增殖和分化对于肌肉再生、疾病建模和培养肉研究的应用至关重要。传统的基于荧光的检测方法虽然敏感,但劳力密集,终点受限,并且破坏肌管的完整性。方法:在这项研究中,我们提出了一种新的高对比度明场(HCBF)成像技术,用于高通量,无标记评估卫星细胞增殖和肌源性分化。使用BioTek Cytation 5自动成像仪和Gen5软件(Agilent Technologies),我们优化了成像参数,以实现标准96孔和384孔格式的连续、高时间分辨率的定量,而无需任何额外的试剂或细胞操作。结果:我们的方法实现了卫星细胞行为的详细动力学分析,揭示了肌管形成动力学,物种特异性培养基反应,最佳播种条件以及机械因素对分化的影响。我们还证明了无血清培养基配方可以支持牛和猪卫星细胞中有效的肌管形成,而与含血清样品相比,具有非常不同的肌管动力学和形态。此外,我们强调了井与井之间的高度差异,培养中肌管的零星形成和脱离,以及在含血清样品中分离后形成第二波肌管的有趣现象。此外,384孔格式使无标记筛选方法能够评估分离卫星细胞的克隆肌原性。结论:通过消除对基因标记、侵入性染色或专门耗材的需要,我们的高通量HCBF方法推进了肌源性研究,为培养肉和肌肉骨骼研究的无血清培养基开发、药物发现和病理生理测试提供了高效筛选和高度详细的动力学数据获取的新机会。
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来源期刊
Stem Cell Reviews and Reports
Stem Cell Reviews and Reports 医学-细胞生物学
CiteScore
9.30
自引率
4.20%
发文量
0
审稿时长
3 months
期刊介绍: The purpose of Stem Cell Reviews and Reports is to cover contemporary and emerging areas in stem cell research and regenerative medicine. The journal will consider for publication: i) solicited or unsolicited reviews of topical areas of stem cell biology that highlight, critique and synthesize recent important findings in the field. ii) full length and short reports presenting original experimental work. iii) translational stem cell studies describing results of clinical trials using stem cells as therapeutics. iv) papers focused on diseases of stem cells. v) hypothesis and commentary articles as opinion-based pieces in which authors can propose a new theory, interpretation of a controversial area in stem cell biology, or a stem cell biology question or paradigm. These articles contain more speculation than reviews, but they should be based on solid rationale. vi) protocols as peer-reviewed procedures that provide step-by-step descriptions, outlined in sufficient detail, so that both experts and novices can apply them to their own research. vii) letters to the editor and correspondence. In order to facilitate this exchange of scientific information and exciting novel ideas, the journal has created five thematic sections, focusing on: i) the role of adult stem cells in tissue regeneration; ii) progress in research on induced pluripotent stem cells, embryonic stem cells and mechanism governing embryogenesis and tissue development; iii) the role of microenvironment and extracellular microvesicles in directing the fate of stem cells; iv) mechanisms of stem cell trafficking, stem cell mobilization and homing with special emphasis on hematopoiesis; v) the role of stem cells in aging processes and cancerogenesis.
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