Intercellular communication
Intercellular communication (ICC) refers to the various ways and structures that biological cells use to communicate with each other directly or through their environment. Often the environment has been thought of as the extracellular spaces within an animal. More broadly cells may also communicate with other animals, either of their own group or species, or other species in the wider ecosystem. Different types of cells use different proteins and mechanisms to communicate with one another using extracellular signalling molecules or electric fluctuations which could be likened to an intercellular ethernet.[2] Components of each type of intercellular communication may be involved in more than one type of communication[2] making attempts at clearly separating the types of communication listed somewhat futile. Broadly speaking, intercellular communication may be categorized as being within a single animal, or between an animal and other animals in the ecosystem in which it lives. In this article intercellular communication has been further collated into various areas of research rather than by functional or structural characteristics.
Communication within an organism
Cell signalling
Molecular cell signaling
Single celled organisms will sense their environment to seek food and may send out signals to other cells to behave symbiotically or reproduce. A classic example of this is the
Cell junctions
Complex organisms may have molecules to hold the cells together which can also be involved in intercellular communication. Some binding molecules are termed the extracellular matrix and may involve longer molecules like cellulose for the cell wall in plants or collagen in animals. When the membranes of two cells are close they may form special types of cell junction which come in five broad types, adherens, desmosomes, gap, tight and tricellular junctions. Adherens, desmosomes, tight and tricellular junctions, serve structural roles. The structures they form also form parts of complex protein signaling pathways.[6] In one respect tight junctions play a generic role in cell signaling in that they may form a tight zip around cells forming an barrier to stop even small unwanted signalling molecules getting between cells.[7] Otherwise signalling molecules may spread to another group of cells which are not requiring the signal or allow signalling molecules escape to quickly from where they are needed.
Pannexins, connexins, innexins
Pannexins, connexins, and innexins are transmembrane proteins that are all named after the Latin term nexus, meaning to connect. They are grouped as they all share a similar structure of 4 transmembrane domains crossing the cell membrane in a similar way but they do not all share enough sequence homology to allow them to be considered directly related.[2][8] Earlier investigations involving the connexins demonstrated cells forming a direct connection with each other using groups of connexins but not connections with the cell exterior. As such they were not considered to participate in the extracellular cell signalling at the time. Later studies made it apparent connexins could connect directly to the cell exterior meaning they are a conduit for the release an uptake of signalling molecules from the environment external to the cell.[9] Furthermore, pannexins appear to do this to such an extent they may rarely if ever participate in direct cell to cell coupling.[10] As indicated on the pannexin/innexin/connexin tree illustrated many animals do not appear to have pannexins/innexins/connexins, perhaps indicating there may be other similar proteins still to be discovered that serve to aid intercellular communication in these animals.[2]
Direct links between cells
Septal pores
In
Most
Plasmodesmata in plants
Plant cells usually have thick cell walls which need to be crossed if neighboring cells are to communicate directly. Plasmodesmata form a pipe through the cell wall forming an ICC. The pipe has another smaller membranous pipe concentric to it connecting the endoplasmic reticulum of the two cells via a tube called the desmotubule. The larger pipe also contains cytoskeletal and other elements. It is presumed viruses use plasmodesmata as a route through the cell walls to spread through the plant.[14]
Gap junctions in animals
Gap junctions can form intercellular links, effectively a tiny direct regulated "pipe" called a connexon pair between the cytoplasms of the two cells that form the junction. 6 connexins make a connexon, 2 connexons make a connexon pair so 12 connexin proteins build each tiny ICC. This ICC allows two cells to communicate directly while being sealed from the outside world.[15] Cells may form one or thousands of these tiny ICCs between them and their other neighbors, potentially forming large networks of directly linked cells. The connexon pairs form ICCs that can transport water, many other molecules up to around 1000 atoms in size[16] and can be very rapidly signaled to turn on and off as required. These ICCs are also communicating electrical signals that can be rapidly turned on and off. To add to their versatility there are a range of these ICC types due to their being over 20 different connexins with different properties that can combine with each other in a variety of ways. The variety of potential signaling combinations that results is enormous. A much studied example of gap junctions electrical signalling abilities is in the electrical synapses found on nerves.[17][18][19] In heart muscle gap junctions function to coordinate the beating of the heart. Adding even further to their versatility gap junctions can also function to form a direct connection to the exterior of a cell paralleling the functioning of the protein cousin the pannexins which are explained elsewhere.
Intercellular bridge
Intercellular bridges are larger than gap junction ICCs so are able to allow the movement of not only small signaling molecules but also large DNA molecules or even whole cell organelles. They are maintained between two cells allowing them to exchange cytoplasmic contents and are frequently observed when cells need intimate communication such as when they are reproducing. They are found in
Cell fusion
Cells that require a more permanent, extensive cytoplasmic linkage may fuse with each other to varying degrees in many cases forming one large cell or syncytium. This happens extensively during the development of
Vesicles
Lipid membrane bound vesicles of a large range of sizes are found inside and outside of cells, containing a huge variety of things ranging from food to invading organisms, water to signaling molecules. Using an electrical nerve impulse from a neuron of a neuromuscular junction to stimulate a muscle to contract is an example of very small[24] (about 0.05μm) vesicles being directly involved in regulating intercellular communication. The neuron produces thousands of tiny vesicles, each containing thousands of signalling molecules. One vesicle is released close to the muscle every second or so when resting. When activated by a nerve impulse more than 100 vesicles will be released at once, hundreds of thousands of signalling molecules, causing a significant contraction of the muscle fiber. All this happens in a small fraction of a second.
Generally small vesicles used to transport signalling molecules released from the cell are termed exosomes[25][26][27] or simply extracellular vesicles (EV),[28] and in addition to their importance to the organism they are also important for biosensors.[24] Extracellular vesicles can be released from malignant cancer cells. These extracellular vesicles have been shown to contain gap junction proteins over-expressed in the malignant cells that spread to non-cancerous cells appearing to enhance the spread of the malignancy.[29] Vesicles are also associated with the transport of materials outside of the cell to enable growth and repair of tissues in the extracellular matrix.[30][31] In situations such as these they may be given special designations such as Matrix Vesicles (MV).
Examples of larger vesicles are in regulatory secretary pathways in