To install click the Add extension button. That's it.

The source code for the WIKI 2 extension is being checked by specialists of the Mozilla Foundation, Google, and Apple. You could also do it yourself at any point in time.

4,5
Kelly Slayton
Congratulations on this excellent venture… what a great idea!
Alexander Grigorievskiy
I use WIKI 2 every day and almost forgot how the original Wikipedia looks like.
Live Statistics
English Articles
Improved in 24 Hours
Added in 24 Hours
Languages
Recent
Show all languages
What we do. Every page goes through several hundred of perfecting techniques; in live mode. Quite the same Wikipedia. Just better.
.
Leo
Newton
Brights
Milds

Intercellular cleft

From Wikipedia, the free encyclopedia

An intercellular cleft is a channel between two cells through which molecules may travel and gap junctions and tight junctions may be present. Most notably, intercellular clefts are often found between epithelial cells and the endothelium of blood vessels and lymphatic vessels, also helping to form the blood-nerve barrier surrounding nerves. Intercellular clefts are important for allowing the transportation of fluids and small solute matter through the endothelium.

YouTube Encyclopedic

  • 1/1
    Views:
    122 516
  • Three types of capillaries | Circulatory system physiology | NCLEX-RN | Khan Academy

Transcription

Let's talk about capillaries. There are actually three major different types of capillaries. I'm going to just kind of sketch out all three. I started with the continuous one. I just drew it out to save us a little bit of time. And the continuous capillary is actually the one that you see most commonly throughout the body. So that's why I wanted to start with this one. A couple of things you'll notice. You'll see that there are four nuclei, so four cells here, making up the part of the capillary we're looking at. And there's a red blood cell moving through it, right? And we actually have the cross section on the right side, so you can actually see, if we were to cut along that face that I've cut, this is what you'd actually see. Now there are two specific things I want to point out. One is that there's a little gap here between these two cells. I'm sketching it in yellow just to really point it out. And that gap is called an intercellular, because it's between cells-- intercellular cleft. So the intercellular cleft is that yellow streak that I just drew. And if I was to point it out on this cross section, it would be right there. You can see the little hole between the two where they don't really meet up. Now there are two more spots I want to point out. One right there and one right there in yellow. And they correspond to this spot and this spot. And there, there is actually really nice joining between the two cells, and we call them tight junctions. Kind of a good name for it, I suppose. You can kind of see why they would call it that. And these tight junctions are right there, labeled with my yellow arrows. Now the one thing I haven't drawn-- I'm going to just sketch out right here-- is in green. And this kind of is a layer beneath all these cells. So these cells are making up the wall of my capillary. But behind them, so that the blood actually doesn't see this layer, except for at the intercellular cleft, is a layer called the basement membrane. So this green stuff that I'm drawing for you, this is our basement membrane. And this basement membrane is basically like a foundation for a house. It's going to keep our cells kind of grounded and keep them in place. And that layer is largely made of protein. Let me now show you a second drawing that I did. This is our second type of capillary. This is a fenestrated capillary. You can see the major difference between this one and the first one is that the second one has little holes, or we call them fenestrations. So this is a fenestrated capillary. And these pores-- I'm going to just label them, and you can also call them pores or holes-- these pores are all over the capillary, right? So we still have, just as before, four cells, four nuclei, and one little red blood cell poking his way through. And you still have the intercellular cleft. So just to show you where it is on this one, it's right there where the two cells really don't meet up so nicely. There's a little gap there. And as before, there's going to be a basement membrane, so let me just kind of sketch out the basement membrane all the way around. And on this cross section, you can see now how I've tried to draw it as best I can to show you the pores, but you have to now get a little creative and see where that intercellular cleft is versus where the pores are. So whenever you're looking at the cross section, it's a little tricky, because you have to almost imagine it in three dimensions. Now the one thing that does help us is the fact that on the inside of these endothelial cells. I'm going to draw in blue a little layer of almost like a slime. And this slime layer is called glycocalyx. And what glycocalyx is is basically sugars that are attached to proteins. And this kind of sugary protein mix is all over the inside layer of these endothelial cells. And so what it does is it actually gets across these pores. So even though there's a pore there, you might get a little bit of glycocalyx spanning the pore. And it'll come across, and it'll look like that. The one place where you won't see it is in the intercellular cleft, because that's actually a real spot between cells. So if you have an intercellular cleft like you do here-- let me just draw the arrow down here, right there-- you won't see any glycocalyx there. So we call that little bit of glycocalyx that's bridging the pore, we call that the diaphragm. So these cells, or these fenestrated capillaries, actually have diaphragms over their pores. But I'm going to put a little star next to that, because sometimes you can find fenestrated capillaries that do not have this glycocalyx that's covering the inside. And they, therefore, do not have diaphragms. So this is something that is generally true, but not always true. So let me show you the third type of capillary then. Let me just show you this last drawing. And this is actually the largest of the capillaries. This one, we call this a discontinuous capillary. And another name for discontinuous capillaries, sometimes they call them sinusoids. So I'm just going to write that up here as well. Sinusoids. So these ones, often found in the liver-- that's kind of the most popular place, or sometimes the spleen as well, or bone marrow-- these ones are actually a few things. They are the largest ones. Let me just make a little list over here. They're very large, and they have a lot more of this intercellular cleft space. Look at all these gaps between the cells, right? And I'm just sketching it in yellow, just to highlight it. But there's a lot of gap here between the cells, meaning that these capillaries end up being very leaky. So in addition to being large, they're very leaky. And a final thing about these guys is that unlike the other two capillaries we just talked about, they have a basement membrane that is often incomplete. So sometimes there are whole areas that are missing basement membrane, just like that. You might have some basement membrane here and here, but you can see whole chunks are missing basement membrane. And maybe there's a bit of basement membrane over here. So let me write that as a third point. Incomplete-- I'm going to write BM for Basement Membrane. Incomplete basement membrane. So if this is the case, it'll be easier for things to kind of escape, even if you have a little glycocalyx here. I'm just drawing a layer of glycocalyx on our discontinuous sinusoid capillary. But even if you have this glycocalyx, because of the fact that you have so much of that intercellular cleft space and you don't have many of the tight junctions, it's going to be easier for things to get out. So moving down these three different types, you're getting more and more leaky as you go down. So just keep that in mind is that the leakiness of the vessel is increasing. In fact, the most leaky is this guy down here, the discontinuous type. So think with me for a second. Let's say you're a molecule in here, in the capillary, and you want to get out here into the tissue. What are the ways you can get there? One way would be if you actually just diffused across, right? So one way could be diffusion. And that would work really well if you're a molecule of oxygen or carbon dioxide. Diffusion works well for those molecules. But let's say you're not one of those molecules. Let's say you're a larger molecule, or a charged molecule, how would you get across? So a second way then to get across could be through a vesicle. Maybe you could get into a vesicle here in this cell, and the vesicle could transport you from being on the inside, which is where this X is, to where it can actually get deposited on the other side. And then, of course, it would still have to make its way through the basement membrane. But that's at least a way of getting past the cell. And so this is a second approach, maybe a vesicle could carry the molecule through. A third way could be through this intercellular cleft. Again, you still have to get across that basement membrane, but at least you can get across the cell by simply going around the cell. So maybe that intercellular cleft could be another ticket to freedom. So if you want to get around, you can go that way. That's a third way. So what's a fourth way? Well, now we have to kind of go down to our second drawing, the fenestrated one. And here. I would suggest maybe just going through-- that little x-- maybe just going through that pore. And you have to plow your way through the glycocalyx, if there is some there. But maybe that's another way is going through the fenestration. That could be another way across, right? So these are four ways for things on the inside to get to the outside. And as you look at this list that we made, these four options, you can see then that our idea around leakiness makes sense, because now, especially when you get down to the discontinuous vessels at the bottom, you've got large gaps between the cells, lots of intercellular clefts. You've got vesicles that can apply anywhere. Diffusion can apply anywhere. And you've got the fenestration. So really, every opportunity for things to get out of the capillaries is available in those discontinuous or sinusoid capillaries.

Dimensions of intercellular cleft

The dimensions of intercellular clefts vary throughout the body, however cleft lengths have been determined for a series of capillaries. The average cleft length for capillaries is about 20m/cm2. The depths of the intercellular clefts, measured from the luminal to the abluminal openings, vary among different types of capillaries, but the average is about 0.7 μm. The width of the intercellular clefts is about 20 nm outside the junctional region (i.e. in the larger part of the clefts). In intercellular clefts of capillaries, it has been calculated that the fractional area of the capillary wall occupied by the intercellular cleft is 20m/cm2 x 20 nm (length x width)= 0.004 (0.4%). This is the fractional area of the capillary wall exposed for free diffusion of small hydrophilic solutes and fluids5.

Communication via cleft

The intercellular cleft is imperative for cell-cell communication. The cleft contains gap junctions, tight junctions, desmosomes, and adheren proteins, all of which help to propagate and/or regulate cell communication through signal transduction, surface receptors, or a chemogradient. In order for a molecule to be taken into the cell either by endocytosis, phagocytosis, or receptor-mediated endocytosis, often that molecule must first enter through the cleft. The intercellular cleft itself is a channel, but what flows through the channel, like ions, fluid, and small molecules and what proteins or junctions give order to the channel is critical for the life of the cells that border the intercellular cleft.

Research utilizing cleft communication

Research at the cell level can deliver proteins, ions, or specific small molecules into the intercellular cleft as a means of injecting a cell. This method is especially useful in cell-to-cell propagation of infectious cytosolic protein aggregates. In one study, protein aggregates from yeast prions were released into a mammalian intercellular cleft and were taken up by the adjacent cell, as opposed to direct cell transfer. This process would be similar to the secretion and transmission of infectious particles through the synaptic cleft between cells of the immune system, as seen in retroviruses. Understanding the routes of intercellular protein aggregate transfer, particularly routes involving clefts is imperative in understanding the progressive spreading of this infection8.

Transport in intercellular cleft

Endothelial tight junctions are most commonly found in the intercellular cleft and provide for regulation of diffusion through the membranes. These links are most commonly found in the most apical aspect of the intercellular cleft. They prevent macromolecules from navigating the intercellular cleft and limit the lateral diffusion of intrinsic membrane proteins and lipids between the apical and basolateral cell surface domains. In the intercellular clefts of capillaries, tight junctions are the first structural barriers a neutrophil encounters as it penetrates the interendothelial cleft, or the gap linking the blood vessel lumen with the subendothelial space2. In capillary endothelium, plasma communicates with the interstitial fluid through the intercellular cleft. Blood plasma without the plasma proteins, red blood cells, and platelets pass through the intercellular cleft and into the capillary7.

Capillary intercellular clefts

Most notably, intercellular clefts are described in capillary blood vessels. The three types of capillary blood vessels are continuous, fenestrated, and discontinuous, with continuous being the least porous of the three and discontinuous capillaries being extremely high in permeability. Continuous blood capillaries have the smallest intercellular clefts, with discontinuous blood capillaries having the largest intercellular clefts, commonly accompanied with gaps in the basement membrane6.Often, fluid is forced out of the capillaries through the intercellular clefts. Fluid is push out through the intercellular cleft at the arterial end of the capillary because that's where the pressure is the highest. However, most of this fluid returns into the capillary at the venous end, creating capillary fluid dynamics. Two opposing forces achieve this balance; hydrostatic pressure and colloid osmotic pressure, using the intercellular clefts are fluid entrances and fluid exits4. In addition, the size of the intercellular clefts and pores in the capillary will influence this fluid exchange. The larger the intercellular cleft, the lesser the pressure and the more fluid will flow out the cleft. This enlargement of the cleft is caused by contraction of capillary endothelial cells, often by substances such as histamine and bradykinin. However, smaller intercellular clefts do not help this fluid exchange3. Along with fluid, electrolytes are also carried through this transport in the capillary blood vessels4. This mechanism of fluid, electrolyte, and also small solute exchange is especially important in renal glomerular capillaries3.

Intercellular cleft and BHB

Intercellular clefts also play a role in the formation of the blood-heart barrier (BHB). The intercellular cleft between endocardial endotheliocytes is 3 to 5 times deeper than the clefts between myocardial capillary endotheliocytes. Also, these clefts are often more twisting and have one or two tight junctions and zona adherens interacting with a circumferential actin filament band and several connecting proteins7. These tight junctions localize to the luminal side of the intercellular clefts, where the glycocalyx, which is important in cell–cell recognition and cell signaling, is more developed. The organization of the endocardial endothelium and the intercellular cleft help to establish the blood-heart barrier by ensuring an active transendothelial physicochemical gradient of various ions1.

References

  1. Thiriet, M. (2015). Interactions between cardiac cell populations. In Diseases of the cardiac pump (1st ed., Vol. 7, pp. 59–61). Paris: Springer.
  2. Gabrilovich, D. (2013). Mechanisms of neutrophil migration. In The neutrophils new outlook for old cells (3rd ed., pp. 138–144). London: Imperial College Press;.
  3. Klabunde, R. (2014, April 30). Mechanisms of capillary exchange. Retrieved 2015, from http://www.cvphysiology.com/Microcirculation/M016.htm
  4. Marieb, E.N. (2003). Essentials of Human Anatomy and Physiology (Seventh ed.). San Francisco: Benjamin Cummings. ISBN 0-8053-5385-2.
  5. Chien, S. (1988). Mathematical models of intercellular clefts. In Vascular endothelium in health and disease (Vol. 242, pp. 3–5). New York City, New York: Plenum Press.
  6. Capillaries. (n.d.). Retrieved from http://www.udel.edu/biology/Wags/histopage/vascularmodelingpage/circsystempage/capillaries/capillaries.html
  7. Silberberg, A.(1988). Structure of the interendothelial cell cleft. Biorheology, 25(1–2),303–18.
  8. Hofmann, J., Denner, P., Naussbaum- Krammer, C., Kuhn, P., Suhre, M., Scheibel, T., ... Vorberg, I. (2013). Cell-to-cell propagation of infectious cytosolic protein aggregates. Proceedings of the National Academy of Sciences of the United States of America, 110(15), 5951–5956–5951–5956. doi:10.1073/pnas.1217321110

External links

This page was last edited on 9 March 2023, at 09:24
Basis of this page is in Wikipedia. Text is available under the CC BY-SA 3.0 Unported License. Non-text media are available under their specified licenses. Wikipedia® is a registered trademark of the Wikimedia Foundation, Inc. WIKI 2 is an independent company and has no affiliation with Wikimedia Foundation.