Satellite glial cell
Satellite cells surrounding the cell bodies of sensory neurons
|NeuroLex ID||Satellite Cell|
Satellite glial cells are glial cells that cover the surface of nerve cell bodies in sensory, sympathetic and parasympathetic ganglia. Both satellite glial cells (SGCs) and Schwann cells – the cells that sheath some nerve fibers – are derived from the neural crest of the embryo during development. SGCs have been found to hold a variety of roles, including control over the microenvironment of sympathetic ganglia. They are thought to have a similar role to astrocytes in the central nervous system (CNS). They supply nutrients to the surrounding neurons and also have some structural function. Satellite cells also act as protective, cushioning cells. Additionally, they express a variety of receptors that allow for a range of interactions with neuroactive chemicals. Many of these receptors and other ion channels have recently been implicated in health issues including chronic pain and herpes simplex. There is much more to be learned about these cells, and research surrounding additional properties and roles of the SGCs is ongoing.
- 1 Anatomy
- 2 Function
- 3 Roles in health issues
- 4 Research directions
- 5 References
Satellite glial cells are the principle glial cells found in the peripheral nervous system, specifically in sensory, sympathetic, and parasympathetic ganglia. They compose the thin cellular sheaths that surround the individual neurons in these ganglia.
In an SGC, the cell body is denoted by the region containing the single, relatively large nucleus. Each side of the cell body extends outward, forming perineuronal processes. The region containing the nucleus has the largest volume of cytoplasm, making this region of the SGC sheath thicker. The sheath can be even thicker if multiple SGCs are layered on top of one another, each measuring 0.1 micrometres (3.9×10−6 in).
Despite their flattened shape, satellite glial cells contain all common organelles necessary to make cellular products and to maintain the homeostatic environment of the cell. The plasma membrane of SGCs is thin and not very dense, and it is associated with adhesion molecules, receptors for neurotransmitters and other molecules, and ion channels, specifically potassium ion channels. Within individual SGCs, there is both rough endoplasmic reticulum and smooth endoplasmic reticulum, but the latter is much less abundant. Most often the Golgi apparatus and the centrioles in an SGC are found in a region very close to the cell’s nucleus. On the other hand, mitochondria are found throughout the cytoplasm along with the organelles involved in autophagy and other forms of catabolic degradation, such as lysosomes, lipofuscin granules, and peroxisomes. Both microtubules and intermediate filaments can be seen throughout the cytoplasm, and most often they lie parallel to the SGC sheath. These filaments are found in greater concentrations at the axon hillock and at the beginning portion of an axon in an SGC of the sympathetic ganglia. In some SGCs of the sensory ganglia researchers have seen a single cilium that extends outward from the cell surface near the nucleus and into the extracellular space of a deep indentation in the plasma membrane. The cilium, however, only has the nine pairs of peripheral microtubules while it lacks the axial pair of microtubules, making its structure very similar to the cilia of neurons, Schwann cells, and astrocytes of the CNS.
In sensory ganglia
Satellite glial cells in sensory ganglia are laminar cells that most often lack any true processes extending from the cell body. In general an envelope of multiple SGCs completely surrounds each sensory neuron. The number of SGCs that make up the sheath increases proportionately with the volume of the neuron which it surrounds. Additionally, the volume of the sheath itself increases proportionately with the volume and surface area of the neuron’s somata. The distance of extracellular space between the sheath and the neuronal plasma membrane measures 20 nanometres (7.9×10−7 in), allowing the neuron and its SGC sheath to form a single anatomical and functional unit. These individual units are separated by areas of connective tissue. However, there are some sensory neurons that occupy the same space within connective tissue and are therefore grouped together in a “cluster” of two or three neurons. Most often each individual neuron in a cluster is still surrounded by its own SGC sheath, but in some cases it is missing. Some sensory neurons have small projections called microvilli that extend outward from their cell surfaces. Due to their close proximity to the SGC sheath, these microvilli of the neuronal plasma membrane reach into the grooves of the sheath, allowing for possible exchange of materials between the cells.
In sympathetic ganglia
In the sympathetic ganglia, satellite glial cells are one of three main types of cells, the other two being the sympathetic ganglion neurons and small intensely fluorescent (SIF) cells. SIF cells of sympathetic ganglia are separated into groups, each of which is surrounded by an SGC sheath. The SGCs of the sympathetic ganglia come from the neural crest and do not proliferate during embryonic development until the neurons are present and mature, indicating that the neurons signal the division and maturation of the SGCs. The SGCs of sympathetic ganglia follow the same basic structure as the SGCs of sensory ganglia, except that sympathetic ganglia also receive synapses. Therefore, the SGC sheath of sympathetic neurons must extend even further to cover the axon hillock near the somata. Like the regions of the sheath near the glial nucleus, the regions of the sheath at the axon hillocks are thicker than those surrounding the rest of the neuron. This indicates that the SGCs play a role in the synaptic environment, thereby influencing synaptic transmission.
Differences from other glial cells
Many people liken SGCs to the astrocytes of the CNS because they share certain anatomical and physiological properties, such as the presence of neurotransmitter transporters and the expression of glutamine synthetase. However, there are distinguishing factors that put SGCs in their own distinct category of glial cells. SGCs most often surround individual sensory and parasympathetic neurons with a complete, unbroken sheath while most neurons of sympathetic ganglia lack a completely continuous SGC sheath, allowing for limited direct exchange of materials between the extracellular space of the neuron and the space within the connective tissue where the SGCs are situated. Furthermore, gap junctions exist between SGCs in the sheaths of adjacent neurons as well as between SGCs in the same sheath (reflexive gap junctions). These gap junctions have been identified through the use of electron microscopy and weight tracer markers, such as Lucifer yellow or neurobiotin. The degree to which SGCs are coupled to SGCs of another sheath or to SGCs of the same sheath is dependent on the pH of the cellular environment.
From studies on rats and mice, researchers have found that satellite glial cells express many neurotransmitter receptors, such as muscarinic acetylcholine and erythropoietin receptors. In order to differentiate between SGCs and other glial cells researchers have used markers to identify which proteins are found in different cells. Although SGCs express glial fibrillary acidic protein (GFAP)and different S-100 proteins, the most useful marker available today for SGC identification is glutamine synthetase (GS). The levels of GS are relatively low at rest, but they greatly increase if the neuron undergoes axonal damage. Furthermore, SGCs also possess mechanisms to release cytokines, adenosine triphosphate (ATP), and other chemical messengers.
Research is currently ongoing in determining the physiological role of satellite glial cells. Current theories suggest that SGCs have a significant role in controlling the microenvironment of the sympathetic ganglia. This is based on the observation that SGCs almost completely envelop the neuron and can regulate the diffusion of molecules across the cell membrane. It has been previously shown that when fluorescent protein tracers are injected into the cervical ganglion in order to bypass the circulatory system, they are not found on the neuron surface. This suggests that the SGCs can regulate the extracellular space of individual neurons. Some speculate that SGCs in the autonomic ganglia have a similar role to the blood–brain barrier as a functional barrier to large molecules.
SGCs role as a regulator of neuronal microenvironment is further characterized by its electrical properties which are very similar to that of astrocytes. Astrocytes have a well studied and defined role in controlling the microenvironment within the brain, therefore researchers are investigating any homologous role of SGCs within the sympathetic ganglia. An established mode of controlling the microenvironment in sensory ganglia is the uptake of substances by specialized transporters which carry neurotransmitters into cells when coupled with Na+ and Cl−. Transporters for glutamate and gamma-Aminobutyric acid (GABA) have been found in SGCs. They appear to be actively engaged in the control of the composition of the extracellular space of the ganglia. The enzyme glutamine synthetase, which catalyzes the conversion of glutamate into glutamine, is found in large amounts in SGCs. Additionally, SGCs contain the glutamate related enzymes glutamate dehydrogenase and pyruvate carboxylase, and thus can supply the neurons not only with glutamine, but also with malate and lactate.
Unlike their adjacent neurons, SGCs do not have synapses but are equipped with receptors for a variety of neuroactive substances that are analogous to those found in neurons. Axon terminals as well as other parts of the neuron carry receptors to substances such as acetylcholine (ACh), GABA, glutamate, ATP, noradrenaline, substance P, and capsaicin that directly affect the physiology of these cells. Current research is revealing that SGCs are also able to respond to some of the same chemical stimuli as neurons. The research is ongoing and SGCs role in injury repair mechanisms is not yet fully understood.
Molecular characteristics of SGCs
|Molecule||Type of Ganglia||Method of Detection||Comments|
|Glutamine synthetase||Mouse TG||IHC||Catalyzes the condensation of glutamate and ammonia to form glutamine|
|GFAP||Rat DRG, TG||IHC||Upregulated by nerve damage|
|S100||Rat DRG||IHC||Upregulated by nerve damage|
|Endothelin ETB receptor||Rat, rabbit DRG||IHC, autoradiography||Blockers of ETs are shown to alleviate pain in animal models|
|Bradykinin B2 receptor||Rat DRG||Electrophysiology||Involved in the inflammatory process|
|P2Y receptor||Mouse TG||Ca2+ imaging, IHC||Contributes to nociception|
|ACh muscarinic receptor||Rat DRG||IHC, mRNA (ISH)||Role not well defined in sensory ganglia|
|NGF trkA receptor||Rat DRG||Immuno-EM||May play a role in response to neuronal injury|
|TGFα||Rat DRG||mRNA (ISH), IHC||Stimulates neural proliferation after injury|
|Erythropoietin receptor||Rat DRG||IHC|
|TNF-α||Mouse DRG, TG||IHC||Inflammatory mediator increased by nerve crush, herpes simplex activation|
|IL-6||Mouse TG||IHC||Cytokine released during inflammation, increased by UV irradiation|
|ERK||Rat DRG||IHC||Involved in functions including the regulation of meiosis, and mitosis|
|JAK2||Rat DRG||IHC||Signaling protein apart of the type II cytokine receptor family|
|Somatostatin sst1 receptor||Rat DRG||IHC||Somatostatin inhibits the release of many hormones and other secretory proteins|
|GABA transporter||Rat DRG||Autoradiography|
|Glutamate transporter||Rat DRG||mRNA (ISH), IHC, Autoradiography||Terminates the excitatory neurotransmitter signal by removal (uptake) of glutamate|
|Guanylate cyclase||Rat DRG, TG||IHC for cGMP||Second messenger that internalizes the message carried by intercellular messengers such as peptide hormones and NO|
|PGD synthase||Chick DRG||IHC||Known to function as a neuromodulator as well as a trophic factor in the central nervous system|
Roles in health issues
Glial cells, including SGCs, have long been recognized for their roles in response to neuronal damage and injury. SCGs have specifically been implicated in a new role involving the creation and persistence of chronic pain, which may involve hyperalgesia and other forms of spontaneous pain.
Secretion of bioactive molecules
SGCs have the ability to release cytokines and other bioactive molecules that transmit pain neuronally. Neurotrophins and tumor necrosis factor α (TNFα) are other cellular factors that work to sensitize neurons to pain. SGCs are present in the PNS in fewer numbers than other more well-known types of glial cells, like astrocytes, but have been determined to have an impact on nociception because of some of their physiological and pharmacological properties. In fact, just like astrocytes, SGCs have the ability to sense and regulate neighboring neuronal activity. First, after a period of nerve cell injury, SGCs are known to up-regulate GFAP and to undergo cell division. They have the ability to release chemoattractants, which are analogous to those released by Schwann cells and contribute to the recruitment and proliferation of macrophages. Additionally, several research groups have found that SGC coupling increases after nerve damage, which has an effect on the perception of pain, likely for several reasons. Normally, the gap junctions between SGCs are used in order to redistribute potassium ions between adjacent cells. However, in coupling of SGCs, the number of gap junctions greatly increases. This may possibly be to deal with larger amounts of ATP and glutamate, which eventually leads to increased recycling of the glutamate. The increased levels of glutamate lead to over excitation and an increase in nociception.
Expression of receptors and ion channels
Various neuronal receptors present on SGCs have been named as participants in ATP-evoked pain signals, particularly the homomultimer P2X3 and the heteromultimer P2X2/3 purinoceptors. In general, the P2X family of receptors responds to neuronally released ATP. Each of the P2X subtypes are found in sensory neurons with the exception of the P2X7 receptor, which is selectively expressed by glial cells, including SGCs. The receptor has been implicated in the release of interleukin IL-1β from macrophages or microglia and astrocytes. The receptor likely has a part in the cascade of events that end with inflammation and neuropathic pain. It has been discovered that this receptor has an antagonist in the form of A-317491, which, when present, has the ability to reduce both the evoked and unprompted firing of various classes of spinal neurons, as well as to inhibit release of IL-1β. However, the outside influences of receptors P2X3 and P2Y1 are believed to complicate the interactions between P2X7 and its antagonist, making it a non-ideal target when using pharmacological strategy.
P2Y receptors are also found on both neurons and glial cells. Their role is less clear than that of the P2X receptors, but it has been noted they have several conflicting functions. In some cases, these receptors act as analgesics, as P2Y1 has the ability to inhibit the action of P2X3. In other cases, the receptors contribute to nociception through the modulation of the extracellular concentration of calcitonin gene related peptide (CGRP). These conflicting roles are being researched further so that they may serve as potential targets for the development of a variety of therapeutic drugs.
SGCs also express a specific type of channel, the Kir4.1 channel, which works to maintain the desired low extracellular K+ concentration in order to control hyperexcitability, which is known to cause migraines. Additionally, extracellular K+ concentration has been found to be controlled by guanine nucleoside guanosine (Guo). Guo, which may be involved in neuron-to-SGC communication and interaction in sensory ganglia, is also a potential target that could control the alterations of extracellular K+ concentration associated with chronic pain.
Sensory ganglia have been associated with infections from viruses like herpes simplex, which can exist in a dormant state within the ganglia for decades after the primary infection. When the virus becomes reactivated, blisters on the skin and mucous membranes appear. During the latent stage of the virus, the viruses are rarely located in the SGCs within the sensory ganglia, but the SGCs may still play an important role within the disease. It has been proposed that SGCs act to create walls to prevent the spread of the virus from infected to uninfected neurons. If this wall of protection was to break down, then the infection could become more widespread. This property may be explained by looking at the location and arrangement of the SGCs, as they are centered on the neurons, allowing them to protect the neurons. It has also been proposed that SGCs may have a job in ridding the ganglia of the virus and in protecting and repairing the nervous system after the virus has left the dormant stage.
The majority of the information available on the subject of SGCs comes from research which was focused on the sensory neurons that the SGCs surround rather than the SGCs themselves. In the future, researchers plan to give more time and attention to the SGCs, which have many supportive and protective functions essential for life. Neurotransmitter and hormone receptors on SGCs in situ rather than in culture will likely be explored and definitively characterized. Changes in the receptors caused by various mutations and diseases will also be explored in order to determine the impact of these conditions. Additionally, the mechanisms behind neuronal-SGC communication is essentially unidentified, though it is likely that the various receptors both the neurons and SGCs have are used for chemical signaling, perhaps with P2Y. Ca2+ and NO and their impacts must also be observed to gain further understanding of interactions between the two types of cells. Finally, the possibility of an influence of SGCs on synaptic transmission within autonomic ganglia provides another direction for future research.
- Hanani M (June 2005). "Satellite glial cells in sensory ganglia: from form to function". Brain Res. Brain Res. Rev. 48 (3): 457–76. doi:10.1016/j.brainresrev.2004.09.001. PMID 15914252.
- Hanani M (September 2010). "Satellite glial cells in sympathetic and parasympathetic ganglia: in search of function". Brain Res Rev 64 (2): 304–27. doi:10.1016/j.brainresrev.2010.04.009. PMID 20441777.
- Hall AK, Landis SC (September 1992). "Division and migration of satellite glia in the embryonic rat superior cervical ganglion". J. Neurocytol. 21 (9): 635–47. doi:10.1007/bf01191725. PMID 1403009.
- Shinder V, Devor M (September 1994). "Structural basis of neuron-to-neuron cross-excitation in dorsal root ganglia". J. Neurocytol. 23 (9): 515–31. doi:10.1007/bf01262054. PMID 7815085.
- Villa G, Fumagalli M, Verderio C, Abbracchio MP, Ceruti S (February 2010). "Expression and contribution of satellite glial cells purinoceptors to pain transmission in sensory ganglia: an update". Neuron Glia Biol. 6 (1): 31–42. doi:10.1017/S1740925X10000086. PMID 20604978.
- Levin MJ, Cai GY, Manchak MD, Pizer LI (June 2003). "Varicella-zoster virus DNA in cells isolated from human trigeminal ganglia". J. Virol. 77 (12): 6979–87. doi:10.1128/jvi.77.12.6979-6987.2003. PMC 156183. PMID 12768016.
- Hanani M (February 2010). "Satellite glial cells: more than just 'rings around the neuron'". Neuron Glia Biol. 6 (1): 1–2. doi:10.1017/S1740925X10000104. PMID 20604976.
- Dixon JS (January 1969). "Changes in the fine structure of satellite cells surrounding chromatolytic neurons". Anat. Rec. 163 (1): 101–9. doi:10.1002/ar.1091630112. PMID 5763130.
- Pannese E (February 2010). "The structure of the perineuronal sheath of satellite glial cells (SGCs) in sensory ganglia". Neuron Glia Biol. 6 (1): 3–10. doi:10.1017/S1740925X10000037. PMID 20604977.
- Mirsky R, Jessen KR, Schachner M, Goridis C (December 1986). "Distribution of the adhesion molecules N-CAM and L1 on peripheral neurons and glia in adult rats". J. Neurocytol. 15 (6): 799–815. doi:10.1007/bf01625196. PMID 3819781.
- Hibino H, Horio Y, Fujita A, et al. (October 1999). "Expression of an inwardly rectifying K(+) channel, Kir4.1, in satellite cells of rat cochlear ganglia". Am. J. Physiol. 277 (4 Pt 1): C638–44. PMID 10516093.
- HESS A (December 1955). "The fine structure of young and old spinal ganglia". Anat. Rec. 123 (4): 399–423. doi:10.1002/ar.1091230403. PMID 13292772.
- Citkowitz E, Holtzman E (January 1973). "Peroxisomes in dorsal root ganglia". J. Histochem. Cytochem. 21 (1): 34–41. doi:10.1177/21.1.34. PMID 4694538.
- Pannese E (July 1964). "Number And Structure Of Perisomatic Satellite Cells Of Spinal Ganglia Under Normal Conditions Or During Axon Regeneration And Neuronal Hypertrophy". Z Zellforsch Mikrosk Anat 63: 568–92. doi:10.1007/bf00339491. PMID 14254752.
- Pannese E (1981). "The satellite cells of the sensory ganglia". Adv Anat Embryol Cell Biol 65: 1–111. PMID 7013430.
- Pannese E, Ledda M, Arcidiacono G, Rigamonti L (May 1991). "Clusters of nerve cell bodies enclosed within a common connective tissue envelope in the spinal ganglia of the lizard and rat". Cell Tissue Res. 264 (2): 209–14. doi:10.1007/BF00313957. PMID 1878941.
- Pannese E (2002). "Perikaryal surface specializations of neurons in sensory ganglia". Int. Rev. Cytol. 220: 1–34. doi:10.1016/S0074-7696(02)20002-9. PMID 12224547.
- Elfvin LG (January 1968). "A new granule-containing nerve cell in the inferior mesenteric ganglion of the rabbit". J. Ultrastruct. Res. 22 (1): 37–44. doi:10.1016/s0022-5320(68)90048-8. PMID 5653898.
- Elfvin LG (November 1971). "Ultrastructural studies on the synaptology of the inferior mesenteric ganglion of the cat. I. Observations on the cell surface of the postganglionic perikarya". J. Ultrastruct. Res. 37 (3): 411–25. PMID 4331152.
- Jasmin L, Vit JP, Bhargava A, Ohara PT (February 2010). "Can satellite glial cells be therapeutic targets for pain control?". Neuron Glia Biol. 6 (1): 63–71. doi:10.1017/S1740925X10000098. PMC 3139431. PMID 20566001.
- Ichikawa H, Jacobowitz DM, Sugimoto T (February 1997). "S100 protein-immunoreactive primary sensory neurons in the trigeminal and dorsal root ganglia of the rat". Brain Res. 748 (1–2): 253–7. doi:10.1016/S0006-8993(96)01364-9. PMID 9067472.
- Allen DT, Kiernan JA (April 1994). "Permeation of proteins from the blood into peripheral nerves and ganglia". Neuroscience 59 (3): 755–64. doi:10.1016/0306-4522(94)90192-9. PMID 8008217.
- Ten Tusscher MP, Klooster J, Vrensen GF (June 1989). "Satellite cells as blood-ganglion cell barrier in autonomic ganglia". Brain Res. 490 (1): 95–102. doi:10.1016/0006-8993(89)90434-4. PMID 2474362.
- Bowery NG, Brown DA, Marsh S (August 1979). "gamma-Aminobutyric acid efflux from sympathetic glial cells: effect of 'depolarizing' agents". J. Physiol. (Lond.) 293: 75–101. PMC 1280703. PMID 501652.
- Alvarez-Leefmans FJ, León-Olea M, Mendoza-Sotelo J, Alvarez FJ, Antón B, Garduño R (2001). "Immunolocalization of the Na(+)-K(+)-2Cl(-) cotransporter in peripheral nervous tissue of vertebrates". Neuroscience 104 (2): 569–82. doi:10.1016/S0306-4522(01)00091-4. PMID 11377856.
- Berger UV, Hediger MA (June 2000). "Distribution of the glutamate transporters GLAST and GLT-1 in rat circumventricular organs, meninges, and dorsal root ganglia". J. Comp. Neurol. 421 (3): 385–99. doi:10.1002/(SICI)1096-9861(20000605)421:3<385::AID-CNE7>3.0.CO;2-S. PMID 10813794.
- Miller KE, Richards BA, Kriebel RM (August 2002). "Glutamine-, glutamine synthetase-, glutamate dehydrogenase- and pyruvate carboxylase-immunoreactivities in the rat dorsal root ganglion and peripheral nerve". Brain Res. 945 (2): 202–11. doi:10.1016/S0006-8993(02)02802-0. PMID 12126882.
- Julius D, Basbaum AI (September 2001). "Molecular mechanisms of nociception". Nature 413 (6852): 203–10. doi:10.1038/35093019. PMID 11557989.
- Gosselin RD, Suter MR, Ji RR, Decosterd I (October 2010). "Glial cells and chronic pain". Neuroscientist 16 (5): 519–31. doi:10.1177/1073858409360822. PMC 3017463. PMID 20581331.
- Steiner I (August 1996). "Human herpes viruses latent infection in the nervous system". Immunol. Rev. 152: 157–73. doi:10.1111/j.1600-065X.1996.tb00915.x. PMID 8930672.
- LaVail JH, Topp KS, Giblin PA, Garner JA (August 1997). "Factors that contribute to the transneuronal spread of herpes simplex virus". J. Neurosci. Res. 49 (4): 485–96. doi:10.1002/(SICI)1097-4547(19970815)49:4<485::AID-JNR9>3.0.CO;2-4. PMID 9285524.
- Wilkinson R, Leaver C, Simmons A, Pereira RA (August 1999). "Restricted replication of herpes simplex virus in satellite glial cell cultures clonally derived from adult mice". J. Neurovirol. 5 (4): 384–91. doi:10.3109/13550289909029479. PMID 10463860.
- Elson K, Speck P, Simmons A (May 2003). "Herpes simplex virus infection of murine sensory ganglia induces proliferation of neuronal satellite cells". J. Gen. Virol. 84 (Pt 5): 1079–84. doi:10.1099/vir.0.19035-0. PMID 12692271.
- Weick M, Cherkas PS, Härtig W, et al. (2003). "P2 receptors in satellite glial cells in trigeminal ganglia of mice". Neuroscience 120 (4): 969–77. doi:10.1016/S0306-4522(03)00388-9. PMID 12927203.