Biology:Cytoplasm
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| The animal cell | |
 Components of a typical animal cell:
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In cell biology, the cytoplasm describes all material within a eukaryotic cell, enclosed by the cell membrane, except for the cell nucleus. The material inside the nucleus and contained within the nuclear membrane is termed the nucleoplasm. The main components of the cytoplasm are the cytosol (a gel-like substance), the organelles (the cell's internal sub-structures), and various cytoplasmic inclusions. The cytoplasm is about 80% water and is usually colorless.[1]
The submicroscopic ground cell substance, or cytoplasmic matrix, that remains after the exclusion of the cell organelles and particles is groundplasm. It is the hyaloplasm of light microscopy, a highly complex, polyphasic system in which all resolvable cytoplasmic elements are suspended, including the larger organelles such as the ribosomes, mitochondria, plant plastids, lipid droplets, and vacuoles.
Many cellular activities take place within the cytoplasm, such as many metabolic pathways, including glycolysis, photosynthesis, and processes such as cell division. The concentrated inner area is called the endoplasm and the outer layer is called the cell cortex, or ectoplasm.
Movement of calcium ions in and out of the cytoplasm is a signaling activity for metabolic processes.[2]
In plants, movement of the cytoplasm around vacuoles is known as cytoplasmic streaming.
History
The term was introduced by Rudolf von Kölliker in 1863, originally as a synonym for protoplasm, but later it has come to mean the cell substance and organelles outside the nucleus.[3][4]
There has been certain disagreement on the definition of cytoplasm, as some authors prefer to exclude from it some organelles, especially the vacuoles[5] and sometimes the plastids.[6]
Physical nature
It remains uncertain how the various components of the cytoplasm interact to allow movement of organelles while maintaining the cell's structure. The flow of cytoplasmic components plays an important role in many cellular functions which are dependent on the permeability of the cytoplasm.[7] An example of such function is cell signalling, a process which is dependent on the manner in which signaling molecules are allowed to diffuse across the cell.[8] While small signaling molecules like calcium ions are able to diffuse with ease, larger molecules and subcellular structures often require aid in moving through the cytoplasm.[9] The irregular dynamics of such particles have given rise to various theories on the nature of the cytoplasm.
As a sol-gel
There has long been evidence that the cytoplasm behaves like a sol-gel.[10] It is thought that the component molecules and structures of the cytoplasm behave at times like a disordered colloidal solution (sol) and at other times like an integrated network, forming a solid mass (gel). This theory thus proposes that the cytoplasm exists in distinct fluid and solid phases depending on the level of interaction between cytoplasmic components, which may explain the differential dynamics of different particles observed moving through the cytoplasm. A papers suggested that at length scale smaller than 100 nm, the cytoplasm acts like a liquid, while in a larger length scale, it acts like a gel.[11]
As a glass
It has been proposed that the cytoplasm behaves like a glass-forming liquid approaching the glass transition.[9] In this theory, the greater the concentration of cytoplasmic components, the less the cytoplasm behaves like a liquid and the more it behaves as a solid glass, freezing more significant cytoplasmic components in place (it is thought that the cell's metabolic activity can fluidize the cytoplasm to allow the movement of such more significant cytoplasmic components).[9] A cell's ability to vitrify in the absence of metabolic activity, as in dormant periods, may be beneficial as a defense strategy. A solid glass cytoplasm would freeze subcellular structures in place, preventing damage, while allowing the transmission of tiny proteins and metabolites, helping to kickstart growth upon the cell's revival from dormancy.[9]
Other perspectives
Research has examined the motion of cytoplasmic particles independent of the nature of the cytoplasm. In such an alternative approach, the aggregate random forces within the cell caused by motor proteins explain the non-Brownian motion of cytoplasmic constituents.[12]
Constituents
The three major elements of the cytoplasm are the cytosol, organelles and inclusions.
Cytosol
The cytosol is the portion of the cytoplasm not contained within membrane-bound organelles. Cytosol makes up about 70% of the cell volume and is a complex mixture of cytoskeleton filaments, dissolved molecules, and water. The cytosol's filaments include the protein filaments such as actin filaments and microtubules that make up the cytoskeleton, as well as soluble proteins and small structures such as ribosomes, proteasomes, and the mysterious vault complexes.[13] The inner, granular and more fluid portion of the cytoplasm is referred to as endoplasm.
Due to this network of fibres and high concentrations of dissolved macromolecules, such as proteins, an effect called macromolecular crowding occurs and the cytosol does not act as an ideal solution. This crowding effect alters how the components of the cytosol interact with each other.
Organelles
Organelles (literally "little organs") are usually membrane-bound structures inside the cell that have specific functions. Some major organelles that are suspended in the cytosol are the mitochondria, the endoplasmic reticulum, the Golgi apparatus, vacuoles, lysosomes, and in plant cells, chloroplasts.
Cytoplasmic inclusions
The inclusions are small particles of insoluble substances suspended in the cytosol. A huge range of inclusions exist in different cell types, and range from crystals of calcium oxalate or silicon dioxide in plants,[14][15] to granules of energy-storage materials such as starch,[16] glycogen,[17] or polyhydroxybutyrate.[18] A particularly widespread example are lipid droplets, which are spherical droplets composed of lipids and proteins that are used in both prokaryotes and eukaryotes as a way of storing lipids such as fatty acids and sterols.[19] Lipid droplets make up much of the volume of adipocytes, which are specialized lipid-storage cells, but they are also found in a range of other cell types.
Controversy and research
The cytoplasm, mitochondria, and most organelles are contributions to the cell from the maternal gamete. Contrary to the older information that disregards any notion of the cytoplasm being active, new research has shown it to be in control of movement and flow of nutrients in and out of the cell by viscoplastic behavior and a measure of the reciprocal rate of bond breakage within the cytoplasmic network.[20]
The material properties of the cytoplasm remain an ongoing investigation. A method of determining the mechanical behaviour of living cell mammalian cytoplasm with the aid of optical tweezers has been described.[21]
See also
- Biology:Amoeboid movement – Mode of locomotion in eukaryotic cells
- Biology:Cytoplasmic streaming – Flow of the cytoplasm inside the cell
- Biology:Protoplasm – Alternative term for cytoplasm or cytoplasm and nucleoplasm
- Biology:Syncytium – Type of multinucleate cell
References
- ↑ The cytomatrix as a cooperative system of macromolecular and water networks. Current Topics in Developmental Biology. 75. 2006. pp. 171–223. doi:10.1016/S0070-2153(06)75006-2. ISBN 9780121531751.
- ↑ Hogan, C. Michael (2010). "Calcium". Encyclopedia of Earth. National Council for Science and the Environment. http://www.eoearth.org/article/Calcium?topic=49557.
- ↑ von Kölliker, Rudolf (1863). "4. Auflage". Handbuch der Gewebelehre des Menschen. Leipzig: Wilhelm Engelmann. https://books.google.com/books?id=5mtARc4NAi0C.
- ↑ Dictionary of the history of science. Princeton University Press. 1981. ISBN 9781400853410. https://books.google.com/books?id=Ian_AwAAQBAJ.
- ↑ "Protoplasmic resistance to water deficits". Water deficits and plant growth, Vol. III. Plant responses and control of water balance.. New York: Academic Press. 1972. pp. 125–176. ISBN 9780323153010. https://books.google.com/books?id=gOEr2alLRUYC.
- ↑ "Ueber den Theilungsvorgang der Zellkerne und das Verhältnis der Kernteilung zur Zellteilung". Arch Mikr Anat 21: 476–590. 1882. doi:10.1007/BF02952628. https://www.biodiversitylibrary.org/item/49525#page/536/mode/1up.
- ↑ "Spatial Modeling of Cell Signaling Networks". Computational Methods in Cell Biology. 110. 2012. pp. 195–221. doi:10.1016/B978-0-12-388403-9.00008-4. ISBN 9780123884039.
- ↑ "Longitudinal diffusion in retinal rod and cone outer segment cytoplasm: the consequence of cell structure". Biophysical Journal 86 (4): 2566–82. April 2004. doi:10.1016/S0006-3495(04)74312-X. PMID 15041693. Bibcode: 2004BpJ....86.2566H.
- ↑ 9.0 9.1 9.2 9.3 "The bacterial cytoplasm has glass-like properties and is fluidized by metabolic activity". Cell 156 (1–2): 183–94. January 2014. doi:10.1016/j.cell.2013.11.028. PMID 24361104. Bibcode: 2014APS..MARJ16002P.
- ↑ "The contractile vacuole in Euplotes: An example of the sol-gel reversibility of cytoplasm". Journal of Experimental Zoology 37 (3): 259–289. 1923. doi:10.1002/jez.1400370302. Bibcode: 1923JEZ....37..259T.
- ↑ Kwapiszewska, Karina et al. (31 July 2020). "Nanoscale Viscosity of Cytoplasm Is Conserved in Human Cell Lines". The Journal of Physical Chemistry Letters 11 (16): 6914–6920. doi:10.1021/acs.jpclett.0c01748. PMID 32787203.
- ↑ "Probing the stochastic, motor-driven properties of the cytoplasm using force spectrum microscopy". Cell 158 (4): 822–832. August 2014. doi:10.1016/j.cell.2014.06.051. PMID 25126787.
- ↑ "The vault complex". Cellular and Molecular Life Sciences 60 (9): 1828–37. September 2003. doi:10.1007/s00018-003-3030-y. PMID 14523546.
- ↑ Prychid, Christina J.; Rudall, Paula J. (1999). "Calcium Oxalate Crystals in Monocotyledons: A Review of their Structure and Systematics". Annals of Botany 84 (6): 725–739. doi:10.1006/anbo.1999.0975. https://academic.oup.com/aob/article-pdf/84/6/725/7983834/840725.pdf.
- ↑ "Systematics and Biology of Silica Bodies in Monocotyledons". The Botanical Review 69 (4): 377–440. 2004. doi:10.1663/0006-8101(2004)069[0377:SABOSB2.0.CO;2].
- ↑ "From bacterial glycogen to starch: understanding the biogenesis of the plant starch granule". Annual Review of Plant Biology 54: 207–233. 2003. doi:10.1146/annurev.arplant.54.031902.134927. PMID 14502990.
- ↑ "New perspectives on the storage and organization of muscle glycogen". Canadian Journal of Applied Physiology 27 (2): 179–203. April 2002. doi:10.1139/h02-012. PMID 12179957.
- ↑ "Occurrence, metabolism, metabolic role, and industrial uses of bacterial polyhydroxyalkanoates". Microbiological Reviews 54 (4): 450–472. December 1990. doi:10.1128/MMBR.54.4.450-472.1990. PMID 2087222.
- ↑ "The biogenesis and functions of lipid bodies in animals, plants and microorganisms". Progress in Lipid Research 40 (5): 325–438. September 2001. doi:10.1016/S0163-7827(01)00013-3. PMID 11470496.
- ↑ "Dictyostelium cells' cytoplasm as an active viscoplastic body". European Biophysics Journal 30 (4): 284–94. August 2001. doi:10.1007/s002490100135. PMID 11548131.
- ↑ "Size- and speed-dependent mechanical behavior in living mammalian cytoplasm". Proc. Natl. Acad. Sci. U.S.A. 114 (36): 9529–9534. September 2017. doi:10.1073/pnas.1702488114. PMID 28827333. Bibcode: 2017PNAS..114.9529H.
External links
- Luby-Phelps K (2000). "Cytoarchitecture and physical properties of cytoplasm: volume, viscosity, diffusion, intracellular surface area". Microcompartmentation and Phase Separation in Cytoplasm. International Review of Cytology. 192. 189–221. doi:10.1016/S0074-7696(08)60527-6. ISBN 9780123645968. http://www.rpgroup.caltech.edu/courses/aph161/Handouts/Luby-Phelps2000.pdf.
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