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通过代谢物摄取和释放的差异缩放建立细胞大小依赖性生长速率。

Establishment of cell size-dependent growth rate via differential scaling of metabolite uptake and release.

作者信息

Meliala Ian, Chen Jingyuan, Lyu Jiahang, Björklund Mikael

机构信息

Centre for Cellular Biology and Signalling, Zhejiang University-University of Edinburgh Institute, Zhejiang University School of Medicine, Haining 314400, China.

University of Edinburgh Medical School, Biomedical Sciences, College of Medicine and Veterinary Medicine, University of Edinburgh, Edinburgh EH8 9JZ, United Kingdom.

出版信息

Proc Natl Acad Sci U S A. 2025 Jun 10;122(23):e2425347122. doi: 10.1073/pnas.2425347122. Epub 2025 Jun 6.

Abstract

Metabolism fuels cell growth and functions. While it is well established that cellular growth rate scales with cell size, how cells alter their metabolism as they change size remains largely unexplored. Here, we conducted a systematic analysis of cell size-dependent metabolism across the NCI60 cancer cell line panel comprising a diverse range of cell sizes. We demonstrate that cellular metabolism and growth rate display 2/3 allometric scaling due to differential scaling of overall nutrient uptake and waste metabolite release with respect to cell size, with waste elimination decreasing less rapidly than nutrient uptake rate as cells grow larger. This results in cell size-dependent growth rate and predicts a maximum cell size where net nutrient uptake equals zero and cell enlargement ceases despite active metabolism. We experimentally confirm this prediction and identify that electron acceptor demand constrains cell enlargement as evidenced by depletion of intracellular aspartate and scaling of aspartate uptake, which is more than proportional to cell volume. Overall, these findings may have implications for understanding cell size homeostasis, developmental biology, and the design principles of living organisms.

摘要

新陈代谢为细胞生长和功能提供能量。虽然细胞生长速率与细胞大小成比例这一点已得到充分证实,但细胞在大小变化时如何改变其新陈代谢在很大程度上仍未得到探索。在这里,我们对包含各种不同细胞大小的NCI60癌细胞系面板进行了细胞大小依赖性新陈代谢的系统分析。我们证明,由于总体营养物质摄取和废物代谢产物释放相对于细胞大小的差异缩放,细胞新陈代谢和生长速率呈现2/3异速生长缩放,随着细胞变大,废物清除的减少速度比营养物质摄取速率慢。这导致了细胞大小依赖性生长速率,并预测了一个最大细胞大小,在该大小下净营养物质摄取等于零,尽管有活跃的新陈代谢,细胞增大仍会停止。我们通过实验证实了这一预测,并确定电子受体需求限制了细胞增大,细胞内天冬氨酸的消耗和天冬氨酸摄取的缩放证明了这一点,天冬氨酸摄取的缩放与细胞体积的比例超过了正比关系。总体而言,这些发现可能对理解细胞大小稳态、发育生物学和生物体的设计原则具有启示意义。

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