Moving cells can sense and respond to physical features of the microenvironment; however, in vivo, the significance of tissue topography is mostly unknown. Here, we usedDrosophilaborder cells, an established model for in vivo cell migration, to study how chemical and physical information influences path selection. Although chemical cues were thought to be sufficient, live imaging, genetics, modeling, and simulations show that microtopography is also important. Chemoattractants promote predominantly posterior movement, whereas tissue architecture presents orthogonal information, a path of least resistance concentrated near the center of the egg chamber. E-cadherin supplies a permissive haptotactic cue. Our results provide insight into how cells integrate and prioritize topographical, adhesive, and chemoattractant cues to choose one path among many.
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SNAP-tagging live cells via chelation-assisted copper-catalyzed azide–alkyne cycloaddition
The sequential biochemical (SNAP-tag) and chemical (chelation-assisted copper-catalyzed azide–alkyne cycloaddition) reactions are applied in membrane protein labeling on live cells. The second, chemical step is rapid (within 1 minute) without any ill-effect to the labeled cells.
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- Award ID(s):
- 1955262
- PAR ID:
- 10528593
- Publisher / Repository:
- Royal Chemical Society
- Date Published:
- Journal Name:
- Organic & Biomolecular Chemistry
- Volume:
- 21
- Issue:
- 36
- ISSN:
- 1477-0520
- Page Range / eLocation ID:
- 7419 to 7436
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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