(Press-News.org) VIDEO:
Nucleoli (green), small liquid-like nuclear bodies, are kept small and afloat by a fine actin mesh. When the mesh breaks, the nucleoli quickly being to fall and coalesce into larger...
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Everybody knows that cells are microscopic, but why? Why aren't cells bigger? The average animal cell is 10 microns across and the traditional explanation has been cells are the perfect size because if they were any bigger it would be difficult to get enough nutrients and energy to support them. Which is roughly where things stood until last year when Princeton bioengineers Marina Feric and Cliff Brangwynne published a paper in Nature Cell Biology (http://www.nature.com/ncb/journal/v15/n10/full/ncb2830.html) describing their probing of cellular inner space, the cell nucleus, and their discovery that gravity could limit cell size.
The researchers studied the mechanics of the cell nucleus using eggs from the African clawed frog, Xenopus laevis. (Bio factoid: scientists who work in Xenopus call each other "froggers.") As cells go, Xenopus eggs are enormous. The Xenopus egg nucleus alone is bigger than most of the cells found in humans. If the average human cell is the size of an average American house, frog eggs are the size of the Empire State Building! Feric and Brangwynne want to know more about the mechanics of these skyscraper-sized cells.
At the ASCB/IFCB meeting in Philadelphia, Feric and Brangwynne will take the gravity story one step further on December 8, describing how giant Xenopus egg cells manage to support thousands of membrane-less compartments inside the nucleus. Most cellular compartments are surrounded by membranes, but some aren't. They're like beer without a bottle or sheep without a fence. There's nothing to really support them or keep them separate. They don't seem to be affected by gravity either; otherwise, they would eventually all pool together at the bottom of the nucleus. But yet they don't.
One type of these membrane-less compartments are the nuclear bodies. They are liquid-like drops, made up of RNA and proteins. Inside the nucleus, they act like droplets of vinegar in oil, that is, whenever they get close together, they fuse and sink. And yet unlike the vinegar in salad dressing, all the little nuclear bodies in the nucleus don't clump into one big pool at the bottom. Feric and Brangwynne previously found that an actin mesh was preventing the nuclear bodies from clumping by keeping them small. But how strong was the mesh?
VIDEO:
Two different RNP droplets, nucleoli (red) and histone locus bodies (HLBs) (green), are suspended in the nucleus of the frog oocyte by a nuclear actin mesh. Disrupt the mesh...
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Feric and Brangwynne wanted to measure gravity's pull on nuclear bodies and against the actin mesh that contained them. They injected a tiny magnetic bead into the nucleus and turned on a magnet to add a known force. They found that the actin mesh in the nucleus is softer than jello, but like jello, with some prodding it returns to its original shape. Actin continues to hold up the nuclear bodies against gravity like pieces of fruit in a jello mold, but under rising force, the nuclear jello undergoes sheer thickening, a non-Newtonian property where a liquid becomes more viscous, a property that probably protects the nucleus. At a high enough force though, the actin mesh breaks and can no longer hold up the nuclear bodies.
This suggests that actin's mechanical properties are finely tuned to resist the force of gravity but also allow flexibility and rigidity of the cell nucleus to support life.
INFORMATION:
Nuclear actin counters gravity during cell growth
M. Feric1, C. Brangwynne2; Chemical Engineering, Princeton University, Princeton, NJ, 2Chemical and Biological Engineering, Princeton University, Princeton, NJ
Contacts
Marina Feric
feric.marina@gmail.com
Clifford P. Brangwynne
cbrangwy@Princeton.edu
The authors will present twice at ASCB.
Minisymposium 11: Organization, Quality Control and Remodeling of the Nuclear Boundary,
Monday, December 8
Lightning Talk, 6:19 to 6:25 pm
Room 113B
Poster Session: Actin and Actin-Associated Proteins 3
Tuesday, December 9
Board 162
Presentation 1650
Time 1:30 to 3:00 pm
Media Contacts
John Fleischman
jfleischman@ascb.org
513.706-0212 (mobile)
Carol Blymire
carol@carolblymire.com
301.332.8090 (mobile)
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