Quantifying the relationship between cell proliferation and morphology during development of the face

bioRxiv [Preprint]. 2023 May 12:2023.05.12.540515. doi: 10.1101/2023.05.12.540515.

Abstract

Morphogenesis requires highly coordinated, complex interactions between cellular processes: proliferation, migration, and apoptosis, along with physical tissue interactions. How these cellular and tissue dynamics drive morphogenesis remains elusive. Three dimensional (3D) microscopic imaging poses great promise, and generates elegant images. However, generating even moderate through-put quantified images is challenging for many reasons. As a result, the association between morphogenesis and cellular processes in 3D developing tissues has not been fully explored. To address this critical gap, we have developed an imaging and image analysis pipeline to enable 3D quantification of cellular dynamics along with 3D morphology for the same individual embryo. Specifically, we focus on how 3D distribution of proliferation relates to morphogenesis during mouse facial development. Our method involves imaging with light-sheet microscopy, automated segmentation of cells and tissues using machine learning-based tools, and quantification of external morphology via geometric morphometrics. Applying this framework, we show that changes in proliferation are tightly correlated to changes in morphology over the course of facial morphogenesis. These analyses illustrate the potential of this pipeline to investigate mechanistic relationships between cellular dynamics and morphogenesis during embryonic development.

Keywords: Convolutional Neural Networks; Developmental biology; Image segmentation; Light-Sheet imaging; Morphometrics; Mouse embryo.

Publication types

  • Preprint

Grants and funding

The work was supported by NIH NIDCR R01-DE019638 to R. M. and B. H., NSERC Discovery Grant ##238992 to B. H., a CIHR Foundation grant to B. H. and R. M. a CFI grant #36262 to BH as well as the Alberta Childrens Hospital Foundation. L.L. was supported by an Eyes High postdoctoral fellowship (University of Calgary), R.G. by a CIHR fellowship, M.V-G by an Alberta Children’s Hospital Research Institute Postdoctoral Fellowship and Alberta Innovates Postdoctoral Fellowship in Health Innovation, M.M. by a Cumming School of Medicine and McCaig Institute postdoctoral fellowship, E.B. by a Cumming School of Medicine and McCaig Institute postdoctoral fellowship, A.D. by a CIHR CGS-M studentship, A.M by an NSERC USRA, M.S. by an NSERC USRA, and N.F. by the Canada Research Chairs Program. This research was enabled in part by support provided by WestGrid and Compute Canada (www.computecanada.ca)