When biologists disabled proteins critical for cell movement, the result was dramatic. The membrane, normally a smooth surface enveloping the cell, erupted in spiky projections. This image, which is part of the Life: Magnified exhibit, resembles a supernova. Although it looks like it exploded, the cell pictured is still alive.
To create the image, Rong Li and Praveen Suraneni, NIH-funded cell biologists at the Stowers Institute for Medical Research in Kansas City, Missouri, disrupted two proteins essential to movement in fibroblasts—connective tissue cells that are also important for healing wounds. The first, called ARPC3, is a protein in the Arp2/3 complex. Without it, the cell moves more slowly and randomly . Inhibiting the second protein gave this cell its spiky appearance. Called myosin IIA (green in the image), it’s like the cell’s muscle, and it’s critical for movement. The blue color is DNA; the red represents a protein called F-actin.
Li and Suraneni are studying cell movement because it’s vital throughout development. In embryos, cells wriggle to their correct location. In the developing brain, neurons migrate to settle in their designated brain structure. Immune cells move toward bacterial and viral invaders—and skin fibroblasts squirm toward injuries to patch wounds.
Disrupting the proteins crucial for movement can wreak havoc: immune diseases, birth deformities, and even death. On the other hand, blocking cell movement could actually be beneficial in certain circumstances. For example, when a cancer cell breaks away from its primary tumor and migrates, resettling in another part of the body—called metastasis—the results can be deadly.
The views, opinions and positions expressed by these authors and blogs are theirs and do not necessarily represent that of the Bioethics Research Library and Kennedy Institute of Ethics or Georgetown University.