ヒトデ胚の圧力に対する細胞の反応を特定する研究(Study Pinpoints Cellular Response to Pressure in Sea Star Embryos)

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2024-04-07 カリフォルニア大学サンディエゴ校(UCSD)

カリフォルニア大学サンディエゴ校を含む国際チームが、組織の成長に伴う圧力変化に細胞が適応する新たな機構を発見しました。海洋生物であるヒトデの胚をモデルとして使用し、細胞がユニークな形「スキュートイド」を取ることが明らかになりました。この形状は、細胞分裂により細胞密度が増加したコンパクトな上皮組織内で発生し、圧力に耐えるために採用されるものです。この研究はがん研究などの応用への道を開く可能性があり、結果は「Development」に掲載されました。

<関連情報>

細胞密度の局所的・大域的変化が、増殖上皮における3次元充填の再編成を引き起こす Local and global changes in cell density induce reorganisation of 3D packing in a proliferating epithelium

Vanessa Barone,Antonio Tagua,Jesus Á. Andrés-San Román,Amro Hamdoun,Juan Garrido-García,Deirdre C. Lyons,Luis M. Escudero
Development  Published:07 May 2024
DOI:https://doi.org/10.1242/dev.202362

3D segmentation of sea star embryos over time: cell packing and morphological analysis at the cellular level. (A) Schematic representation of wild-type (top) and WT-comp (bottom) sea star embryos. (B) Maximum projections of a representative wild-type sea star embryo (top) or WT-comp embryo (bottom) expressing the membrane marker mYFP at 128-, 256- and 512-cell stages. Scale bars: 50 μm. (C) Computer rendering of the segmented sea star embryo at the 512-cell stage from a frontal (left) and lateral (right) perspective. (D) 3D representation of a four-cell motif with scutoid (top) or frusta (bottom) conformations. The apical and basal z-slices of the motives are shown. Coloured overlays show the section area for each cell in the corresponding 3D representation. (E-I) Quantifications of average scutoid frequency (E), surface ratio anisotropy (F), cell density (G), cell volume (H) and cell convexity (I). Wild type, n=150 timepoints, six embryos, four experiments; WT-comp, n=150 timepoints, six embryos, five experiments for all panels except F (where n=125 timepoints, five embryos, four experiments). Data are mean±s.d. Mann–Whitney tests with Bonferroni multiple comparisons correction (black) and Kruskal–Wallis tests with Dunn multiple comparisons correction (blue), except in F where one-way ANOVA test with Tukey multiple comparison correction was used (light blue); ns, non-significant; *P<0.05; **P<0.01; ***P<0.001.

ABSTRACT

Tissue morphogenesis is intimately linked to the changes in shape and organisation of individual cells. In curved epithelia, cells can intercalate along their own apicobasal axes, adopting a shape named ‘scutoid’ that allows energy minimization in the tissue. Although several geometric and biophysical factors have been associated with this 3D reorganisation, the dynamic changes underlying scutoid formation in 3D epithelial packing remain poorly understood. Here, we use live imaging of the sea star embryo coupled with deep learning-based segmentation to dissect the relative contributions of cell density, tissue compaction and cell proliferation on epithelial architecture. We find that tissue compaction, which naturally occurs in the embryo, is necessary for the appearance of scutoids. Physical compression experiments identify cell density as the factor promoting scutoid formation at a global level. Finally, the comparison of the developing embryo with computational models indicates that the increase in the proportion of scutoids is directly associated with cell divisions. Our results suggest that apico-basal intercalations appearing immediately after mitosis may help accommodate the new cells within the tissue. We propose that proliferation in a compact epithelium induces 3D cell rearrangements during development.

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