Cell migration and the mysterious role of cadherin

What do sled and clusters have in common? According to research by UC Santa Barbara’s Denise , they both travel in groups and need a leader to make sure they all follow in the same direction.

Montell, Duggan Professor of Molecular Cellular and Developmental Biology, and colleagues worked on three independent projects involving E-, a protein found in throughout the body. The researchers used fruit-fly ovaries to uncover the played by E-cadherin in collective . Their findings are reported today in the journal Cell.

According to traditional scientific dogma, E-cadherin acts like the mortar between bricks, holding cells together and preventing motility. Montell’s team found the opposite: Cadherin is actually promoting the ability of cells to move and migrate. “It’s doing it in three different ways in three different parts of the cell,” said. “In each spot in the cell, cadherin is doing something different and all of those function together to orchestrate the movement of cells.”

Montell’s team sought to understand the E-cadherin-mediated of these cells with three separate approaches that converged on one idea: the guidance of cell movement. “This kind of motility is similar to what do when they metastasize,” said, “and it’s part of the normal development of different tissues.”

One researcher studied the interaction between the lead cell and the following cells; hence, the sled-dog analogy. The lead cell is tethered by E-caderin to other cells in the cluster and pulls them in the proper direction in the same way the lead sled dog guides its team.

While E-cadherin is distributed throughout the cell cluster, the lead cell — determined by the strong force of E-cadherin that causes the cell to protrude in the direction of the movement — can communicate with the side and rear cells and prohibit them from protruding. This creates a front and back to the entire cluster of cells.

Lead author Danfeng Cai, a graduate student in the Denise Lab, suppressed cadherin in different cell types and analyzed the visible guidance defects by making movies of the migrating cells. When cells lacked E-cadherin, they were unable to migrate as an organized group, and the direction of their movement was random and irregular.

Another member of the research team designed an optical sensor of mechanical tension — a kind of microscopic spring — and inserted it into the cadherin protein. This enabled the measurement of force on the E-cadherin molecules. The results showed that even though the distribution of the protein was uniform, the force per molecule was stronger at the front. “It’s kind of amazing that you can make that measurement in living cells,” said.

In addition to highlighting E-cadherin’s in cell , the paper introduces new experimental tools the team used to probe and analyze E-cadherin in living tissue, the first

… Continue reading here.
Dogs News — Sciencedaily

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