Researchers in Japan, India and France have found that molecules move into and out of a specialized region of the cell membrane, called the 'raft domain', at unexpectedly fast rates. The discovery was made possible by developing fluorescent compounds that are structurally similar to a special class of lipids called sphingomyelins, and by using a home-built fluorescent microscope sensitive enough to detect single fluorescent molecules.
Sphingomyelins are key molecules for the signalling functions and the formation of raft domains. But how they mediate the domains' signalling functions was unknown.
A team of researchers led by Akihiro Kusumi and Kenichi Suzuki of Kyoto University's Institute for Integrated Cell-Material Sciences (iCeMS) developed fluorescent compounds that are structurally similar to sphingomyelins and behave in a similar way. To make these fluorescent 'analogs', they attached a hydrophilic (water-preferring) fluorescent molecule to the 'head' part of synthetic sphingomyelin, with a hydrophilic linker group between them, without modifying a critical positive charge in the head group. This arrangement ensured that the fluorescent molecule was placed away from the interior of the cell membrane and did not interfere with the function of the sphingomyelin it was attached to or with the function of the cell membrane.
When the fluorescent sphingomyelin analogs were incorporated into the cell membrane of live mammalian cells in culture, they continually and very dynamically entered and exited from the cell membrane's raft domains. Raft domains are extremely small, around 1/1,000th of the width of a human hair. But they occupy 10 to 20% of the cell membrane area. Quite unexpectedly, the sphingomyelins spent only 12 and 50 milliseconds inside the raft domain before and after extracellular immunostimulation respectively. For comparison, the eye blinks in about 400 milliseconds.
Discovering the very short residency times of sphingomyelins in raft domains represents a large paradigm shift in the research field of cell biology, molecular immunology and molecular neuroscience. Previously, most researchers in these fields believed that raft-associated lipids, including sphingomyelins, were stably localized in raft domains.
"The results suggest that the fluorescent sphingomyelin analogs developed here will be extremely useful for studying sphingomyelin interactions with many other raft-associated molecules and raft domains as well as for understanding the mechanisms of cell membrane signalling and of the invasion of various pathogens," the researchers conclude.
The paper "Raft-based sphingomyelin interactions revealed by new fluorescent sphingomyelin analogs" appeared on March 22, 2017 in Journal of Cell Biology, with doi: 10.1083/jcb.201607086
The Institute for Integrated Cell-Material Sciences (iCeMS) at Kyoto University in Japan aims to advance the integration of cell and material sciences, both traditionally strong fields at the university, in a uniquely innovative global research environment. ICeMS combines the biosciences, chemistry, materials science and physics to create materials for mesoscopic cell control and cell-inspired materials. Such developments hold promise for significant advances in medicine, pharmaceutical studies, the environment and industry. http://www.icems.kyoto-u.ac.jp
Journal of Cell Biology