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完整小鼠胫骨的优化活体三光子成像将浆细胞运动与功能状态联系起来。

Optimized intravital three-photon imaging of intact mouse tibia links plasma cell motility to functional states.

作者信息

Rakhymzhan Asylkhan, Fiedler Alexander F, Günther Robert, Domingue Scott R, Wooldridge Laura, Leben Ruth, Cao Yu, Bias Anne, Roodselaar Jay, Köhler Ralf, Ulbricht Carolin, Heidelin Judith, Andresen Volker, Beckers Ingeborg, Haibel Astrid, Duda Georg, Hauser Anja E, Niesner Raluca A

机构信息

German Rheumatism Research Center - a Leibniz Institute, Biophysical Analytics, Berlin, Germany.

German Rheumatism Research Center - a Leibniz Institute, Immune Dynamics, Berlin, Germany.

出版信息

iScience. 2024 Sep 17;27(10):110985. doi: 10.1016/j.isci.2024.110985. eCollection 2024 Oct 18.

Abstract

Intravital deep bone marrow imaging is crucial to studying cellular dynamics and functions but remains challenging, and minimally invasive methods are needed. We employed a high pulse-energy 1650 nm laser to perform three-photon microscopy , reaching ≈400 μm depth in intact mouse tibia. Repetition rates of 3 and 4 MHz allowed us to analyze motility patterns of fast and rare cells within unperturbed marrow and to identify a bi-modal migratory behavior for plasma cells. Third harmonic generation (THG) was identified as a label-free marker for cellular organelles, particularly endoplasmic reticulum, indicating protein synthesis capacity. We found a strong THG signal, suggesting high antibody secretion, in one-third of plasma cells while the rest showed low signals. We discovered an inverse relationship between migratory behavior and THG signal, linking motility to functional plasma cell states. This method may enhance our understanding of marrow microenvironment effects on cellular functions.

摘要

活体深层骨髓成像对于研究细胞动力学和功能至关重要,但仍然具有挑战性,因此需要微创方法。我们使用高脉冲能量1650纳米激光进行三光子显微镜检查,在完整的小鼠胫骨中达到约400微米的深度。3兆赫和4兆赫的重复频率使我们能够分析未受干扰的骨髓中快速移动和罕见细胞的运动模式,并确定浆细胞的双峰迁移行为。三次谐波产生(THG)被确定为细胞器,特别是内质网的无标记标记,表明蛋白质合成能力。我们发现三分之一的浆细胞中有很强的THG信号,表明抗体分泌量高,而其余浆细胞则显示低信号。我们发现迁移行为与THG信号之间存在反比关系,将运动性与功能性浆细胞状态联系起来。这种方法可能会增强我们对骨髓微环境对细胞功能影响的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79d6/11466647/12c4e8740877/fx1.jpg

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