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Soltwedel, J. R.

Publications and source records attributed to Soltwedel, J. R..

2 recordsLinked to original sources

Tissue surface mechanics constrains proliferation-driven forces to guide mammalian body axis elongation

Mammalian embryos undergo complex morphogenetic changes after implantation in the uterus. The elongation of the body along a head-to-tail axis is a pivotal event, as it lays the foundation of the body plan. While genetic and biochemical aspects of mammalian body elongation have been uncovered, the physical mechanism of axial morphogenesis remains unknown, largely due to the inaccessibility of the implanted embryo to physical measurements and manipulations in utero. Gastruloids, a stem-cell-based embryo model of mammalian axial morphogenesis, lift such limitations. Combining live imaging, direct mechanical measurements, and chemical and mechanical perturbations, here we show that axis elongation in mouse and human gastruloids is guided by a posterior actin cap at the tissue surface that constrains the expansive forces of cell proliferation. Measurements of mechanical stresses using oil microdroplets, as well as inhibition of cell proliferation and myosin activity, show that the forces driving elongation arise from cell proliferation, and not from convergent extension movements. We find that isotropic tissue expansion is redirected into posterior elongation by the formation of a supracellular actin cap at the posterior tissue surface that restricts lateral tissue expansion. Finally, we show that posterior elongation in mouse embryos displays the key features of the physical elongation mechanism reported for mouse and human gastruloids. These findings reveal that mammalian body axis elongation, including human, occurs via a different physical mechanism from other vertebrate species.

biophysics↗

Gliding motility of the diatom Craspedostauros australis correlates with the intracellular movement of raphid-specific myosins

Raphid diatoms are one of the few eukaryotes capable of gliding motility, which is remarkably fast and allows for quasi-instantaneous directional reversals. Besides other mechanistic models, it has been suggested that an actomyosin system provides the force for diatom gliding. However, in vivo data on the dynamics of actin and myosin in diatoms are lacking. In this study we demonstrate that the raphe-associated actin bundles required for diatom movement do not exhibit a directional turnover of subunits and thus their dynamics do not contribute directly to force generation. By phylogenomic analysis we identified four raphid diatom-specific myosins in Craspedostauros australis (CaMyoA-D) and investigated their in vivo localization and dynamics through GFP-tagging. Only CaMyoB-D but not CaMyoA exhibited coordinated movement during gliding, consistent with a role in force generation. The characterization of raphid diatom-specific myosins lays the foundation for unraveling the molecular mechanisms that underlie the gliding motility of diatoms.

cell biology↗