From Wikipedia, the free encyclopedia
Figure from original paper, showing line diagrams of phagosomes arising from omegasomes (part D).

The omegasome is a cell organelle consisting of lipid bilayer membranes enriched for phosphatidylinositol 3-phosphate (abbreviated PI(3)P or PtdIns3P), and related to a process of autophagy. [1] It is a subdomain of the endoplasmic reticulum (ER), [2] and has a morphology resembling the Greek capital letter Omega (Ω). Omegasomes are the sites from which phagophores (also called "isolation membranes") form, [1] [2] which are sack-like structures that mature into autophagosomes, and fuse with lysosomes in order to degrade the contents of the autophagosomes. [3] The formation of omegasomes depends on various factors, however in general, formation of omegasomes is increased as a response to starvation, [1] and in some biochemical situations the presence of PI(3)P leads to the formation of omegasomes. [4]

Macroautophagy

Illustration showing steps from omegasome to autolysosome. [5]

Autophagy (from Greek words for "self" and "eating") is a process of digesting or degrading cytoplasmic molecules ( proteins, lipids, sugars and organelles). Macroautophagy is the main autophagic pathway, used primarily to eradicate damaged cell organelles such as mitochondria, [6] ribosomes, etc., which helps in supplying amino acids and energy to the cells, and maintains longevity. [7] Omegasomes positioned on the endoplasmic reticulum, are enriched with PI(3)P and PI(3)P-binding proteins, and responsible for the formation of phagophores. [8] The omegasome is present at the opening of the sack-like phagophore while items destined for degradation by macroautophagy are loaded into the phagophore. There are specific receptor proteins that recruit items to the phagophore. [9] The phagophore expands to accommodate the items, until the omegasome is closed to produce the roughly spherical autophagosome. How autophagosomes are "detached" or "exit" from the omegasome is not clear, but autophagocytosis associated protein Atg3 and other proteins are required. Additionally, collections of thin tubules at the junction between omegasome and phagophore appear to be involved. [10] Actin is also believed to be important. [11] [12] It has been observed that various pathogen infections that lead to the induction of autophagy display the formation of autophagosomes through omegasomes developed as an innate response to the infection. [13]

Function

Omegasomes display significant functional roles in different biochemical pathways which assist in various autophagosome processes. Omegasomes attract the effectors needed to target PI3P, while also ensuring that the autophagosomal membranes fuse with the double membrane vesicles and promote autophagosome formation. [4] Omegasomes act as progenitors of autophagosome formation during the autophagy pathway. [14] There are various autophagosome mediators involved in autophagy, however it is the omegasome regulation of the pathway that provides a smooth transition of autophagosome formation, and enrichment of nutrients in the cells. [14]

References

  1. ^ a b c Axe EL, Walker SA, Manifava M, Chandra P, Roderick HL, Habermann A, Griffiths G, Ktistakis NT, et al. (2008). "Autophagosome formation from membrane compartments enriched in phosphatidylinositol 3-phosphate and dynamically connected to the endoplasmic reticulum". J Cell Biol. 182 (4): 685–701. doi: 10.1083/jcb.200803137. PMC  2518708. PMID  18725538.
  2. ^ a b Biazik J, Ylä-Anttila P, Vihinen H, Jokitalo E, Eskelinen EL (2015). "Ultrastructural relationship of the phagophore with surrounding organelles". Autophagy. 11 (3): 439–51. doi: 10.1080/15548627.2015.1017178. PMC  4502653. PMID  25714487.
  3. ^ Kern A, Dikic I, Behl C (2015). "The integration of autophagy and cellular trafficking pathways via RAB GAPs". Autophagy. 11 (12): 2393–7. doi: 10.1080/15548627.2015.1110668. PMC  4835203. PMID  26565612.
  4. ^ a b Karanasios, Eleftherios; Stapleton, Eloise; Manifava, Maria; Kaizuka, Takeshi; Mizushima, Noboru; Walker, Simon A.; Ktistakis, Nicholas T. (2013-01-01). "Dynamic association of the ULK1 complex with omegasomes during autophagy induction". Journal of Cell Science. 126 (Pt 22): 5224–5238. doi: 10.1242/jcs.132415. ISSN  1477-9137. PMID  24013547. S2CID  1195124.
  5. ^ Kruppa AJ, Kendrick-Jones J, Buss F (2016). "Myosins, Actin and Autophagy". Traffic. 17 (8): 878–90. doi: 10.1111/tra.12410. PMC  4957615. PMID  27146966.
  6. ^ Yang JY, Yang WY (2013). "Bit-by-bit autophagic removal of parkin-labelled mitochondria". Nature Communications. 4: 2428. Bibcode: 2013NatCo...4.2428Y. doi: 10.1038/ncomms3428. PMID  24013556.
  7. ^ Perrotta, Cristiana; Cattaneo, Maria Grazia; Molteni, Raffaella; De Palma, Clara (2020-12-10). "Autophagy in the Regulation of Tissue Differentiation and Homeostasis". Frontiers in Cell and Developmental Biology. 8: 602901. doi: 10.3389/fcell.2020.602901. ISSN  2296-634X. PMC  7758408. PMID  33363161.
  8. ^ Nascimbeni, Anna Chiara; Codogno, Patrice; Morel, Etienne (2017). "Phosphatidylinositol-3-phosphate in the regulation of autophagy membrane dynamics". The FEBS Journal. 284 (9): 1267–1278. doi: 10.1111/febs.13987. ISSN  1742-4658. PMID  27973739. S2CID  1796268.
  9. ^ Kim BW, Kwon DH, Song HK (2016). "Structure biology of selective autophagy receptors". BMB Reports. 49 (2): 73–80. doi: 10.5483/bmbrep.2016.49.2.265. PMC  4915120. PMID  26698872.
  10. ^ Uemura T, Yamamoto M, Kametaka A, Sou YS, Yabashi A, Yamada A, Annoh H, Kametaka S, Komatsu M, Waguri S (2014). "A cluster of thin tubular structures mediates transformation of the endoplasmic reticulum to autophagic isolation membrane". Molecular and Cellular Biology. 34 (9): 1695–706. doi: 10.1128/MCB.01327-13. PMC  3993601. PMID  24591649.
  11. ^ Aguilera MO, Berón W, Colombo MI (2012). "The actin cytoskeleton participates in the early events of autophagosome formation upon starvation induced autophagy". Autophagy. 8 (11): 1590–603. doi: 10.4161/auto.21459. PMC  3494589. PMID  22863730.
  12. ^ Kruppa AJ, Kendrick-Jones J, Buss F (2016). "Myosins, Actin and Autophagy". Traffic. 17 (8): 878–90. doi: 10.1111/tra.12410. PMC  4957615. PMID  27146966.
  13. ^ Roberts, Rebecca; Ktistakis, Nicholas T. (2013-09-27). Lane, Jon D. (ed.). "Omegasomes: PI3P platforms that manufacture autophagosomes". Essays in Biochemistry. 55: 17–27. doi: 10.1042/bse0550017. ISSN  0071-1365. PMID  24070468.
  14. ^ a b Roberts, Rebecca; Ktistakis, Nicholas T. (2013-09-27). Lane, Jon D. (ed.). "Omegasomes: PI3P platforms that manufacture autophagosomes". Essays in Biochemistry. 55: 17–27. doi: 10.1042/bse0550017. ISSN  0071-1365. PMID  24070468.


From Wikipedia, the free encyclopedia
Figure from original paper, showing line diagrams of phagosomes arising from omegasomes (part D).

The omegasome is a cell organelle consisting of lipid bilayer membranes enriched for phosphatidylinositol 3-phosphate (abbreviated PI(3)P or PtdIns3P), and related to a process of autophagy. [1] It is a subdomain of the endoplasmic reticulum (ER), [2] and has a morphology resembling the Greek capital letter Omega (Ω). Omegasomes are the sites from which phagophores (also called "isolation membranes") form, [1] [2] which are sack-like structures that mature into autophagosomes, and fuse with lysosomes in order to degrade the contents of the autophagosomes. [3] The formation of omegasomes depends on various factors, however in general, formation of omegasomes is increased as a response to starvation, [1] and in some biochemical situations the presence of PI(3)P leads to the formation of omegasomes. [4]

Macroautophagy

Illustration showing steps from omegasome to autolysosome. [5]

Autophagy (from Greek words for "self" and "eating") is a process of digesting or degrading cytoplasmic molecules ( proteins, lipids, sugars and organelles). Macroautophagy is the main autophagic pathway, used primarily to eradicate damaged cell organelles such as mitochondria, [6] ribosomes, etc., which helps in supplying amino acids and energy to the cells, and maintains longevity. [7] Omegasomes positioned on the endoplasmic reticulum, are enriched with PI(3)P and PI(3)P-binding proteins, and responsible for the formation of phagophores. [8] The omegasome is present at the opening of the sack-like phagophore while items destined for degradation by macroautophagy are loaded into the phagophore. There are specific receptor proteins that recruit items to the phagophore. [9] The phagophore expands to accommodate the items, until the omegasome is closed to produce the roughly spherical autophagosome. How autophagosomes are "detached" or "exit" from the omegasome is not clear, but autophagocytosis associated protein Atg3 and other proteins are required. Additionally, collections of thin tubules at the junction between omegasome and phagophore appear to be involved. [10] Actin is also believed to be important. [11] [12] It has been observed that various pathogen infections that lead to the induction of autophagy display the formation of autophagosomes through omegasomes developed as an innate response to the infection. [13]

Function

Omegasomes display significant functional roles in different biochemical pathways which assist in various autophagosome processes. Omegasomes attract the effectors needed to target PI3P, while also ensuring that the autophagosomal membranes fuse with the double membrane vesicles and promote autophagosome formation. [4] Omegasomes act as progenitors of autophagosome formation during the autophagy pathway. [14] There are various autophagosome mediators involved in autophagy, however it is the omegasome regulation of the pathway that provides a smooth transition of autophagosome formation, and enrichment of nutrients in the cells. [14]

References

  1. ^ a b c Axe EL, Walker SA, Manifava M, Chandra P, Roderick HL, Habermann A, Griffiths G, Ktistakis NT, et al. (2008). "Autophagosome formation from membrane compartments enriched in phosphatidylinositol 3-phosphate and dynamically connected to the endoplasmic reticulum". J Cell Biol. 182 (4): 685–701. doi: 10.1083/jcb.200803137. PMC  2518708. PMID  18725538.
  2. ^ a b Biazik J, Ylä-Anttila P, Vihinen H, Jokitalo E, Eskelinen EL (2015). "Ultrastructural relationship of the phagophore with surrounding organelles". Autophagy. 11 (3): 439–51. doi: 10.1080/15548627.2015.1017178. PMC  4502653. PMID  25714487.
  3. ^ Kern A, Dikic I, Behl C (2015). "The integration of autophagy and cellular trafficking pathways via RAB GAPs". Autophagy. 11 (12): 2393–7. doi: 10.1080/15548627.2015.1110668. PMC  4835203. PMID  26565612.
  4. ^ a b Karanasios, Eleftherios; Stapleton, Eloise; Manifava, Maria; Kaizuka, Takeshi; Mizushima, Noboru; Walker, Simon A.; Ktistakis, Nicholas T. (2013-01-01). "Dynamic association of the ULK1 complex with omegasomes during autophagy induction". Journal of Cell Science. 126 (Pt 22): 5224–5238. doi: 10.1242/jcs.132415. ISSN  1477-9137. PMID  24013547. S2CID  1195124.
  5. ^ Kruppa AJ, Kendrick-Jones J, Buss F (2016). "Myosins, Actin and Autophagy". Traffic. 17 (8): 878–90. doi: 10.1111/tra.12410. PMC  4957615. PMID  27146966.
  6. ^ Yang JY, Yang WY (2013). "Bit-by-bit autophagic removal of parkin-labelled mitochondria". Nature Communications. 4: 2428. Bibcode: 2013NatCo...4.2428Y. doi: 10.1038/ncomms3428. PMID  24013556.
  7. ^ Perrotta, Cristiana; Cattaneo, Maria Grazia; Molteni, Raffaella; De Palma, Clara (2020-12-10). "Autophagy in the Regulation of Tissue Differentiation and Homeostasis". Frontiers in Cell and Developmental Biology. 8: 602901. doi: 10.3389/fcell.2020.602901. ISSN  2296-634X. PMC  7758408. PMID  33363161.
  8. ^ Nascimbeni, Anna Chiara; Codogno, Patrice; Morel, Etienne (2017). "Phosphatidylinositol-3-phosphate in the regulation of autophagy membrane dynamics". The FEBS Journal. 284 (9): 1267–1278. doi: 10.1111/febs.13987. ISSN  1742-4658. PMID  27973739. S2CID  1796268.
  9. ^ Kim BW, Kwon DH, Song HK (2016). "Structure biology of selective autophagy receptors". BMB Reports. 49 (2): 73–80. doi: 10.5483/bmbrep.2016.49.2.265. PMC  4915120. PMID  26698872.
  10. ^ Uemura T, Yamamoto M, Kametaka A, Sou YS, Yabashi A, Yamada A, Annoh H, Kametaka S, Komatsu M, Waguri S (2014). "A cluster of thin tubular structures mediates transformation of the endoplasmic reticulum to autophagic isolation membrane". Molecular and Cellular Biology. 34 (9): 1695–706. doi: 10.1128/MCB.01327-13. PMC  3993601. PMID  24591649.
  11. ^ Aguilera MO, Berón W, Colombo MI (2012). "The actin cytoskeleton participates in the early events of autophagosome formation upon starvation induced autophagy". Autophagy. 8 (11): 1590–603. doi: 10.4161/auto.21459. PMC  3494589. PMID  22863730.
  12. ^ Kruppa AJ, Kendrick-Jones J, Buss F (2016). "Myosins, Actin and Autophagy". Traffic. 17 (8): 878–90. doi: 10.1111/tra.12410. PMC  4957615. PMID  27146966.
  13. ^ Roberts, Rebecca; Ktistakis, Nicholas T. (2013-09-27). Lane, Jon D. (ed.). "Omegasomes: PI3P platforms that manufacture autophagosomes". Essays in Biochemistry. 55: 17–27. doi: 10.1042/bse0550017. ISSN  0071-1365. PMID  24070468.
  14. ^ a b Roberts, Rebecca; Ktistakis, Nicholas T. (2013-09-27). Lane, Jon D. (ed.). "Omegasomes: PI3P platforms that manufacture autophagosomes". Essays in Biochemistry. 55: 17–27. doi: 10.1042/bse0550017. ISSN  0071-1365. PMID  24070468.



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