Morishita Yoshihiro, Kuroiwa Atsushi, Suzuki Takayuki
Laboratory for Developmental Morphogeometry, RIKEN Quantitative Biology Center, Kobe 650-0047, Japan RIKEN Center for Developmental Biology, Kobe 650-0047, Japan
Division of Biological Science, Graduate School of Science, Nagoya University Furo-cho, Chikusa-ku, Nagoya 464-8602, Japan.
Development. 2015 May 1;142(9):1672-83. doi: 10.1242/dev.109728. Epub 2015 Apr 9.
Tissue-level characterization of deformation dynamics is crucial for understanding organ morphogenetic mechanisms, especially the interhierarchical links among molecular activities, cellular behaviors and tissue/organ morphogenetic processes. Limb development is a well-studied topic in vertebrate organogenesis. Nevertheless, there is still little understanding of tissue-level deformation relative to molecular and cellular dynamics. This is mainly because live recording of detailed cell behaviors in whole tissues is technically difficult. To overcome this limitation, by applying a recently developed Bayesian approach, we here constructed tissue deformation maps for chick limb development with high precision, based on snapshot lineage tracing using dye injection. The precision of the constructed maps was validated with a clear statistical criterion. From the geometrical analysis of the map, we identified three characteristic tissue growth modes in the limb and showed that they are consistent with local growth factor activity and cell cycle length. In particular, we report that SHH signaling activity changes dynamically with developmental stage and strongly correlates with the dynamic shift in the tissue growth mode. We also found anisotropic tissue deformation along the proximal-distal axis. Morphogenetic simulation and experimental studies suggested that this directional tissue elongation, and not local growth, has the greatest impact on limb shaping. This result was supported by the novel finding that anisotropic tissue elongation along the proximal-distal axis occurs independently of cell proliferation. Our study marks a pivotal point for multi-scale system understanding in vertebrate development.
组织水平的变形动力学特征对于理解器官形态发生机制至关重要,尤其是分子活动、细胞行为与组织/器官形态发生过程之间的层级间联系。肢体发育是脊椎动物器官发生中一个研究充分的课题。然而,相对于分子和细胞动力学,对组织水平的变形仍知之甚少。这主要是因为在整个组织中实时记录详细的细胞行为在技术上具有难度。为克服这一限制,我们应用最近开发的贝叶斯方法,基于染料注射的快照谱系追踪,高精度构建了鸡胚肢体发育的组织变形图。所构建图谱的精度通过明确的统计标准得到验证。通过对图谱的几何分析,我们在肢体中识别出三种特征性的组织生长模式,并表明它们与局部生长因子活性和细胞周期长度一致。特别是,我们报告说,SHH信号活性随发育阶段动态变化,并且与组织生长模式的动态转变密切相关。我们还发现沿近端-远端轴存在各向异性的组织变形。形态发生模拟和实验研究表明,这种定向的组织伸长而非局部生长对肢体塑形的影响最大。这一结果得到了一项新发现的支持,即沿近端-远端轴的各向异性组织伸长独立于细胞增殖发生。我们的研究标志着脊椎动物发育多尺度系统理解的一个关键点。