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拓扑结构和细胞核大小决定了生长中的肺类球体上的细胞堆积。

Topology and Nuclear Size Determine Cell Packing on Growing Lung Spheroids.

作者信息

Tang Wenhui, Huang Jessie, Pegoraro Adrian F, Zhang James H, Tang Yiwen, Kotton Darrell N, Bi Dapeng, Guo Ming

机构信息

Department of Mechanical Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA.

Center for Regenerative Medicine of Boston University and Boston Medical Center, Boston, Massachusetts, USA.

出版信息

Phys Rev X. 2025 Jan-Mar;15(1). doi: 10.1103/physrevx.15.011067. Epub 2025 Mar 21.

Abstract

Within multicellular living systems, cells coordinate their positions with spatiotemporal accuracy to form various tissue structures and control development. These arrangements can be regulated by tissue geometry, biochemical cues, as well as mechanical perturbations. However, how cells pack during dynamic three-dimensional multicellular architectures formation remains unclear. Here, examining a growing spherical multicellular system, human lung alveolospheres, we observe an emergence of hexagonal packing order and a structural transition of cells that comprise the spherical epithelium. Surprisingly, the cell packing behavior on the spherical surface of lung alveolospheres resembles hard-disks packing on spheres, where the less deformable cell nuclei act as effective "hard disks" and prevent cells from getting too close. Nucleus-to-cell size ratio increases during lung spheroids growth; as a result, we find more hexagon-concentrated cellular packing with increasing bond orientational order. Furthermore, by osmotically changing the compactness of cells on alveolospheres, we observe a more ordered packing when nucleus-to-cell size ratio increases, and vice versa. These more ordered cell packing characteristics are consistent with reduced cell dynamics, together suggesting that better cellular packing stabilizes local cell neighborhoods and may regulate more complex biological functions such as cellular maturation and tissue morphogenesis.

摘要

在多细胞生命系统中,细胞以时空精确性协调其位置,以形成各种组织结构并控制发育。这些排列可由组织几何形状、生化线索以及机械扰动来调节。然而,在动态三维多细胞结构形成过程中细胞如何堆积仍不清楚。在这里,通过研究一个不断生长的球形多细胞系统——人肺肺泡球,我们观察到六边形堆积秩序的出现以及构成球形上皮的细胞的结构转变。令人惊讶的是,肺肺泡球球形表面上的细胞堆积行为类似于球体上的硬磁盘堆积,其中较不易变形的细胞核充当有效的“硬磁盘”,防止细胞靠得太近。在肺球体生长过程中,核与细胞大小比增加;因此,我们发现随着键取向序增加,六边形集中的细胞堆积更多。此外,通过渗透改变肺泡球上细胞的致密性,我们观察到当核与细胞大小比增加时堆积更有序,反之亦然。这些更有序的细胞堆积特征与细胞动力学降低一致,共同表明更好的细胞堆积稳定了局部细胞邻域,并可能调节更复杂的生物学功能,如细胞成熟和组织形态发生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94fc/12122012/a20b62028f9a/nihms-2083588-f0005.jpg

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