CAMBRIDGE, Mass. (February 10, 2008) Unlike the rest of the cells in your body, your red blood cells lack nuclei. That quirk dates back to the time when mammals began to evolve. Other vertebrates such as fish, reptiles, and birds, have red cells that contain nuclei that are inactive. Losing the nucleus enables the red blood cell to contain more oxygen-carrying hemoglobin, thus enabling more oxygen to be transported in the blood and boosting our metabolism.
Scientists have struggled to understand the mechanism by which maturing red blood cells eject their nuclei. Now, researchers in the lab of Whitehead Member Harvey Lodish have modeled the complete process in vitro in mice, reporting their findings in Nature Cell Biology online on February 10, 2008. The first mechanistic study of how a red blood cell loses its nucleus, the research sheds light on one of the most essential steps in mammalian evolution.
It was known that as a mammalian red blood cell nears maturity, a ring of actin filaments contracts and pinches off a segment of the cell that contains the nucleus, a type of cell division. The nucleus is then swallowed by macrophages (one of the immune systems quick-response troops). The genes and signaling pathways that drive the pinching-off process, however, were a mystery.
Using a cell-culture system we were actually able to watch the cells divide, go through hemoglobin synthesis and then lose their nuclei, says Lodish, who is also a professor of biology at Massachusetts Institute of Technology. We discovered that the proteins Rac 1, Rac 2 and mDia2 are involved in building the ring of actin filaments.
We were very interested in that Rac 1 and Rac 2 were involved in disposing the nuclei of red blood cells, says Peng Ji, lead author and postdoctoral researcher in the Lodish lab. These proteins are known for their role in creating actin fibers in many body cells, and a necessary component of many important cellular functi
|Contact: Cristin Carr|
Whitehead Institute for Biomedical Research