Seed Media Group

Reality is always more complicated than you think.

Profile

jake-head-shot.jpgJake Young is a MD/PhD student at Mount Sinai School of Medicine focusing in Neuroscience. He is due to graduate in 2032. He received a BS and a MS in Biological Sciences from Stanford University -- where he spent most of his time drinking heavily and building vegetable catapults instead of learning information that would now be eminently useful. When he is not failing terrifically to perform his sworn duties, he enjoys watching bad movies, ethnic food, and running.

Pure Pedantry is a blog about science -- social sciences and otherwise -- as well as academic and scientific culture. No one can live on science alone, so I also like to dwell on pop culture, periodically explore the humanities, and indulge in other types of geeky goodness.

Jake is joined periodically by two wonderful guest bloggers: Kara Contreary and Kate Seip. See the About Page.

DISCLAIMERS: 1) Jake Young is not a licensed physician (yet). He is merely a medical student. The information published on this site is not intended for use in medical decision making. Please seek advice from a licensed, medical professional before making any health decisions. 2) The opinions expressed are my own or those of my co-bloggers. They do not represent the views of SEED magazine or the educational establishments we currently attend.

Search this blog

Archives

Blogroll


raptor.jpg

« Do Women Need to Have Periods? | Main | Background to Sen. Tim Johnson's Condition »

Presynaptic Vesicles are Hemifused

Category: Synapses
Posted on: December 14, 2006 10:33 AM, by Jake Young

There has always been a bit of a debate as to whether the vesicles in the presynaptic nerve terminal that contain transmitter are just near the presynaptic membrane or are in fact hemifused with it.

At the presynapse, vesicles containing neurotransmitter are prepared and aligned by the presynaptic membrane -- the process of synaptic release needs to be very rapid. When an action potential travels down the axon, calcium flows into the presynaptic terminal. This calcium activates SNARE proteins that are involved both in docking the vesicles near the membrane and fusing them with the membrane. The vesicle fuses with the membrane, releasing its contents into the synapse.

This is incredibly fast, but scientists have long wondered whether it is fast because the vesicles are already hemifused. What does it mean to be hemifused? The membranes of both vesicles and cells are composed of lipid bilayers. The lipids are a lot like soap. They have a charged water-loving end and uncharged oil-like tail. The oil-like tails like to hug together in order for them to have as little contact with water as possible. The best arrangement for them to do this is a bilayer with the charged ends on the outsides and the tails oriented in towards the middle.

It would be possible for the vesicle to just be floating around intact and tethered to the membrane. However, it is also possible for part of the outer bilayer of the vesicle membrane to have already blended into the inner bilayer of the cell membrane. This would mean that the vesicle could release its contents even more quickly.

Unfortunately it is really difficult to check this proposition. Vesicles and synapses are incredibly small, requiring electron microscopy to even see. However, Zampighi et al, publishing in the Biophysical Journal, used conical electron tomography to show that the majority of docked vesicles are hemifused.

hemifused.jpg

This image shows a small number of vesicles. The blue vesicles are not docked. The red vesicles are hemifused. The white vesicle has fully fused with the membrane and is releasing its contents. The bottom panels show a reconstruction of what it would look like to see a vesicle fusing from outside the cell -- before and after fusion.

full-synapse.jpg

This image shows a larger view. The top panel is an electron micrograph showing the presynaptic and the postsynaptic terminal. The bottom panel color codes the constituents. The red vesicles are hemifused. The blue vesicles are not docked. The orange blobs are the presynaptic web. The white is the synaptic membranes in apposition. The brown is the postsynaptic density.

When the researchers did counts of the vesicles, they found that the vast majority that were docked. Of the docked vesicles about 75% were hemifused. This means that this hemifusion may be one of the reasons the synapse is so fast. For repeated activity you have other vesicles floating around, but for immediate use you have these vesicles ready to go.

Comments

So are the hemi-fused vesicles involved in "kiss-and-run" exocytosis or in some other mechanism?

Posted by: The neurophilosopher | December 14, 2006 12:22 PM

So the idea of "kiss and run" as I understand is suggesting that the vesicle fuses and releases its contents but remains largely intact before being endocytosed -- that it doesn't fully fuse into the membrane. As I understand it, it is more a statement of what happens after exocytosis than where the vesicle is before it.

I think that this shows that is certainly possible that "kiss and run" is happening. You don't really see any full vesicles sliding into the membrane in those pictures, and the fusion pore is very tiny.

Posted by: Jake Young | December 14, 2006 2:55 PM

Cool graphics and great succinct explanation of lipid bilayers. As a civilian, I've always thought of soap, but never seen it mentioned before.

Posted by: SkookumPlanet | December 15, 2006 3:48 PM

I'm sure we'll find that transmitter release, like every other aspect of brain function, is far more complex than we think it is. Full fusion, hemifusion, kiss-and-run, everything in between, and possibly even other novel ways.

Posted by: The neurophilosopher | December 15, 2006 4:35 PM

Speaking of kiss-and-run, I saw a talk recently by Jurgen Klingauf, who presented convincing evidence that the vast majority of vesicles at hippocampal glutamatergic synapses allow their transmembrane proteins to diffuse away from the vesicle upon fusion and intermix thoroughly with the pool in the plasma membrance before re-assorting prior to endocytosis. Very nice work.

Posted by: PhysioProf | December 15, 2006 7:01 PM

Did anyone of you heard about a forthcoming paper, which gives an overview about the recently known members of the CAZ (Cytomatrix of active zone)? I ask for clarification in respect to RIM1 anchoring, the role of ELKS, and the protein meshwork interactions from the 2007 point of view. There are so many changes in the processes of vesicle docking priming in the last year, what else? Im pretty unpatient about that.

Posted by: the big H | September 14, 2007 12:54 PM

14, 2006 10:33 AM?


Hallo?

Does this page still exists?

Posted by: big H | September 14, 2007 1:00 PM

Post a Comment

(Email is required for authentication purposes only. Comments are moderated for spam, your comment may not appear immediately. Thanks for waiting.)





Having problems commenting? (UPDATED)

Blogs in the Network

Advertisement

Top Five: Readers' Picks

Search All Blogs

Top Science Stories

powered by SEED - seedmagazine.com