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Soma (biology)

Soma (biology)

Animation in the reference.

Animation in the reference.

The soma (somas), perikaryon (pl. perikarya), neurocyton, or cell body is the bulbous, non-process portion of a neuron or other brain cell type, containing the cell nucleus. The word 'soma' comes from the Greek 'σῶμα', meaning 'body'. Although it is often used to refer to neurons, it can also refer to other cell types as well, including astrocytes,[1] oligodendrocytes,[2] and microglia.[3] There are many different specialized types of neurons, and their sizes vary from as small as about 5 micrometres to over 10 millimetre for some of the smallest and largest neurons of invertebrates, respectively.

The soma of a neuron (i.e., the main part of the neuron in which the dendrites branch off of) contains many organelles, including granules called Nissl granules, which are composed largely of rough endoplasmic reticulum and free polyribosomes.[4] The cell nucleus is a key feature of the soma. The nucleus is the source of most of the RNA that is produced in neurons. In general, most proteins are produced from mRNAs that do not travel far from the cell nucleus. This creates a challenge for supplying new proteins to axon endings that can be a meter or more away from the soma. Axons contain microtubule-associated motor proteins that transport protein-containing vesicles between the soma and the synapses at the axon terminals. Such transport of molecules towards and away from the soma maintains critical cell functions.

The axon hillock is a specialized domain of the neuronal cell body from which the axon originates. A high amount of protein synthesis occurs in this region, as it contains many Nissl granules (which are ribosomes wrapped in RER) andXXXX polyribosomes. Within the axon hillock, materials are sorted as either items that will enter the axon (like the components of the cytoskeletal architecture of the axon, mitochondria, etc.) or will remain in the soma. In addition, the axon hillock also has a specialized plasma membrane that contains large numbers of voltage-gated ion channels, since this is most often the site of action potential initiation.[4]

The survival of some sensory neurons depends on axon terminals making contact with sources of survival factors that prevent apoptosis. The survival factors are neurotrophic factors, including molecules such as nerve growth factor (NGF). NGF interacts with receptors at axon terminals, and this produces a signal that must be transported up the length of the axon to the nucleus. A current theory of how such survival signals are sent from axon endings to the soma includes the idea that NGF receptors are endocytosed from the surface of axon tips and that such endocytotic vesicles are transported up the axon.[5]

Structure of a typical neuron
Soma
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References

[1]
Citation Link//www.ncbi.nlm.nih.gov/pubmed/26814587Bazargani, N; Attwell, D (February 2016). "Astrocyte calcium signaling: the third wave". Nature Neuroscience. 19 (2): 182–9. doi:10.1038/nn.4201. PMID 26814587.
Sep 29, 2019, 6:50 AM
[2]
Citation Link//www.ncbi.nlm.nih.gov/pubmed/11274346Baumann, N; Pham-Dinh, D (April 2001). "Biology of oligodendrocyte and myelin in the mammalian central nervous system". Physiological Reviews. 81 (2): 871–927. doi:10.1152/physrev.2001.81.2.871. PMID 11274346.
Sep 29, 2019, 6:50 AM
[3]
Citation Link//www.ncbi.nlm.nih.gov/pubmed/22457705Kozlowski, C; Weimer, RM (2012). "An automated method to quantify microglia morphology and application to monitor activation state longitudinally in vivo". PLoS ONE. 7 (2): e31814. doi:10.1371/journal.pone.0031814. PMC 3294422. PMID 22457705.
Sep 29, 2019, 6:50 AM
[4]
Citation Linkopenlibrary.orgSquire, Larry; Berg, Darwin; Bloom, Floyd; du Lac, Sascha; Ghosh, Anirvan; Spitzer, Nicholas, eds. (2008). Fundamental Neuroscience (3rd ed.). Academic Press. ISBN 978-0-12-374019-9.
Sep 29, 2019, 6:50 AM
[5]
Citation Link//www.ncbi.nlm.nih.gov/pubmed/14699953Delcroix JD, Valletta J, Wu C, et al. (2004). Trafficking the NGF signal: implications for normal and degenerating neurons. Prog. Brain Res. Progress in Brain Research. 146. pp. 3–23. doi:10.1016/s0079-6123(03)46001-9. ISBN 9780444514721. PMID 14699953.
Sep 29, 2019, 6:50 AM
[6]
Citation Linkwww.ouhsc.eduHistology image: 3_09
Sep 29, 2019, 6:50 AM
[7]
Citation Linkdiscovery.ucl.ac.uk"Astrocyte calcium signaling: the third wave"
Sep 29, 2019, 6:50 AM
[8]
Citation Linkdoi.org10.1038/nn.4201
Sep 29, 2019, 6:50 AM
[9]
Citation Linkwww.ncbi.nlm.nih.gov26814587
Sep 29, 2019, 6:50 AM
[10]
Citation Linkdoi.org10.1152/physrev.2001.81.2.871
Sep 29, 2019, 6:50 AM
[11]
Citation Linkwww.ncbi.nlm.nih.gov11274346
Sep 29, 2019, 6:50 AM
[12]
Citation Linkwww.ncbi.nlm.nih.gov"An automated method to quantify microglia morphology and application to monitor activation state longitudinally in vivo"
Sep 29, 2019, 6:50 AM
[13]
Citation Linkdoi.org10.1371/journal.pone.0031814
Sep 29, 2019, 6:50 AM
[14]
Citation Linkwww.ncbi.nlm.nih.gov3294422
Sep 29, 2019, 6:50 AM
[15]
Citation Linkwww.ncbi.nlm.nih.gov22457705
Sep 29, 2019, 6:50 AM
[16]
Citation Linkdoi.org10.1016/s0079-6123(03)46001-9
Sep 29, 2019, 6:50 AM
[17]
Citation Linkwww.ncbi.nlm.nih.gov14699953
Sep 29, 2019, 6:50 AM
[18]
Citation Linkwww.ouhsc.eduHistology image: 3_09
Sep 29, 2019, 6:50 AM
[19]
Citation Linken.wikipedia.orgThe original version of this page is from Wikipedia, you can edit the page right here on Everipedia.Text is available under the Creative Commons Attribution-ShareAlike License.Additional terms may apply.See everipedia.org/everipedia-termsfor further details.Images/media credited individually (click the icon for details).
Sep 29, 2019, 6:50 AM