Program in Biological and Biomedical Sciences, Harvard Medical School, Boston, MA 02115, USA; Department of Molecular and Cellular Biology, Harvard University, Cambridge, MA 02138, USA.
Department of Molecular and Cellular Biology, Harvard University, Cambridge, MA 02138, USA.
Curr Biol. 2024 Jun 17;34(12):2672-2683.e4. doi: 10.1016/j.cub.2024.05.014. Epub 2024 May 31.
Cell division without cell separation produces multicellular clusters in budding yeast. Two fundamental characteristics of these clusters are their size (the number of cells per cluster) and cellular composition: the fractions of cells with different phenotypes. Using cells as nodes and links between mother and daughter cells as edges, we model cluster growth and breakage by varying three parameters: the cell division rate, the rate at which intercellular connections break, and the kissing number (the maximum number of connections to one cell). We find that the kissing number sets the maximum possible cluster size. Below this limit, the ratio of the cell division rate to the connection breaking rate determines the cluster size. If links have a constant probability of breaking per unit time, the probability that a link survives decreases exponentially with its age. Modeling this behavior recapitulates experimental data. We then use this framework to examine synthetic, differentiating clusters with two cell types, faster-growing germ cells and their somatic derivatives. The fraction of clusters that contain both cell types increases as either of two parameters increase: the kissing number and difference between the growth rate of germ and somatic cells. In a population of clusters, the variation in cellular composition is inversely correlated (r = 0.87) with the average fraction of somatic cells in clusters. Our results show how a small number of cellular features can control the phenotypes of multicellular clusters that were potentially the ancestors of more complex forms of multicellular development, organization, and reproduction.
细胞分裂而不进行细胞分离会在出芽酵母中产生多细胞簇。这些簇的两个基本特征是其大小(每个簇中的细胞数量)和细胞组成:不同表型细胞的分数。使用细胞作为节点,母细胞和子细胞之间的连接作为边,我们通过改变三个参数来模拟簇的生长和断裂:细胞分裂率、细胞间连接断裂的速率以及亲吻数(一个细胞的最大连接数)。我们发现,亲吻数设定了最大可能的簇大小。在这个限制以下,细胞分裂率与连接断裂率的比值决定了簇的大小。如果连接在单位时间内有一个恒定的断裂概率,那么连接存活的概率随着其年龄呈指数下降。这种行为的建模再现了实验数据。然后,我们使用这个框架来研究具有两种细胞类型(生长更快的生殖细胞及其体细胞衍生物)的合成、分化簇。包含两种细胞类型的簇的比例随着两个参数之一的增加而增加:亲吻数和生殖细胞与体细胞生长率之间的差异。在一群簇中,细胞组成的变化与簇中体细胞的平均分数呈负相关(r=0.87)。我们的研究结果表明,少量的细胞特征可以控制多细胞簇的表型,这些多细胞簇可能是更复杂形式的多细胞发育、组织和繁殖的祖先。