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细胞温度测量在探测生化途径中的考虑因素。

Cellular Thermometry Considerations for Probing Biochemical Pathways.

机构信息

Department of Mechanical Science and Engineering, University of Illinois at Urbana-Champaign, Urbana, IL, 61801, USA.

出版信息

Cell Biochem Biophys. 2021 Jun;79(2):359-373. doi: 10.1007/s12013-021-00979-w. Epub 2021 Apr 2.

Abstract

Temperature is a fundamental thermodynamic property that can serve as a probe of biochemical reactions. Extracellular thermometry has previously been used to probe cancer metabolism and thermoregulation, with measured temperature changes of ~1-2 K in tissues, consistent with theoretical predictions. In contrast, previous intracellular thermometry studies remain disputed due to reports of >1 K intracellular temperature rises over 5 min or more that are inconsistent with theory. Thus, the origins of such anomalous temperature rises remain unclear. An improved quantitative understanding of intracellular thermometry is necessary to provide a clearer perspective for future measurements. Here, we develop a generalizable framework for modeling cellular heat diffusion over a range of subcellular-to-tissue length scales. Our model shows that local intracellular temperature changes reach measurable limits (>0.1 K) only when exogenously stimulated. On the other hand, extracellular temperatures can be measurable (>0.1 K) in tissues even from endogenous biochemical pathways. Using these insights, we provide a comprehensive approach to choosing an appropriate cellular thermometry technique by analyzing thermogenic reactions of different heat rates and time constants across length scales ranging from subcellular to tissues. Our work provides clarity on cellular heat diffusion modeling and on the required thermometry approach for probing thermogenic biochemical pathways.

摘要

温度是一种基本的热力学性质,可以作为生化反应的探针。 细胞外测温法以前曾用于探测癌症代谢和体温调节,在组织中测量到的温度变化约为 1-2 K,与理论预测一致。 相比之下,由于在 5 分钟或更长时间内出现超过 1 K 的细胞内温度升高的报告,以前的细胞内测温研究仍存在争议,这些报告与理论不一致。 因此,这种异常温度升高的原因尚不清楚。 为了为未来的测量提供更清晰的视角,有必要对细胞内测温进行更定量的理解。 在这里,我们开发了一种可推广的框架,用于在亚细胞到组织的各种长度尺度上对细胞热扩散进行建模。 我们的模型表明,只有在外源性刺激下,局部细胞内温度变化才会达到可测量的极限(>0.1 K)。 另一方面,即使来自内源性生化途径,细胞外温度也可以在组织中进行测量(>0.1 K)。 利用这些见解,我们通过分析不同热率和时间常数的产热反应,在从亚细胞到组织的各种长度尺度上,提供了一种选择合适细胞测温技术的综合方法。 我们的工作为细胞热扩散建模以及探测产热生化途径所需的测温方法提供了明确性。

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