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词条 Neutrophil elastase
释义

  1. Gene

  2. Function

  3. Clinical significance

  4. Inhibitors

  5. See also

  6. References

  7. Further reading

  8. External links

{{Infobox_gene}}Neutrophil elastase ({{EC number|3.4.21.37}}, leukocyte elastase, ELANE, ELA2, elastase 2, neutrophil, elaszym, serine elastase, subtype human leukocyte elastase (HLE)) is a serine proteinase in the same family as chymotrypsin and has broad substrate specificity. Secreted by neutrophils and macrophages during inflammation, it destroys bacteria and host tissue.[1] It also localizes to Neutrophil extracellular traps (NETs), via its high affinity for DNA, an unusual property for serine proteases.[2]

As with other serine proteinases it contains a charge relay system composed of the catalytic triad of histidine, aspartate, and serine residues that are dispersed throughout the primary sequence of the polypeptide but that are brought together in the three dimensional conformation of the folded protein. The gene encoding neutrophil elastase, ELA2, consists of five exons. Neutrophil elastase is closely related to other cytotoxic immune serine proteases, such as the granzymes and cathepsin G. It is more distantly related to the digestive CELA1.[2]

The neutrophil form of elastase ({{EC number|3.4.21.37}}) is 218 amino acids long, with two asparagine-linked carbohydrate chains (see glycosylation). It is present in azurophil granules in the neutrophil cytoplasm. There appear to be two forms of neutrophil elastase, termed IIa and IIb.

Gene

In humans, neutrophil elastase is encoded by the ELANE gene, which resides on chromosome 19.[3]

Function

Elastases form a subfamily of serine proteases that hydrolyze many proteins in addition to elastin. Humans have six elastase genes that encode the structurally similar proteins elastase 1, 2, 2A, 2B, 3A, and 3B. Neutrophil elastase hydrolyzes proteins within specialized neutrophil lysosomes, called azurophil granules, as well as proteins of the extracellular matrix following the protein's release from activated neutrophils. Neutrophil elastase may play a role in degenerative and inflammatory diseases by its proteolysis of collagen-IV and elastin of the extracellular matrix. This protein degrades the outer membrane protein A (OmpA) of E. coli as well as the virulence factors of such bacteria as Shigella, Salmonella and Yersinia.[4] Mutations in this gene are associated with cyclic neutropenia and severe congenital neutropenia (SCN). This gene is clustered with other serine protease gene family members, azurocidin 1 and proteinase 3 genes, at chromosome 19pter. All 3 genes are expressed coordinately and their protein products are packaged together into azurophil granules during neutrophil differentiation.[5]

Clinical significance

Neutrophil elastase is an important protease enzyme that when expressed aberrantly can cause emphysema or emphysematous changes. This involves breakdown of the lung structure and increased airspaces. Mutations of the ELANE gene cause severe congenital neutropenia, which is a failure of neutrophils to mature.[6]

Inhibitors

In order to minimize damage to tissues, there are few inhibitors of neutrophil elastase. One group of inhibitors are the Serpins (Serine Protease Inhibitors).[7] Neutrophil elastase has been shown to interact with Alpha 2-antiplasmin, which belongs to the Serpin family of proteins.[8][9]

See also

  • Elastase

References

1. ^{{cite journal | vauthors = Belaaouaj A, Kim KS, Shapiro SD | title = Degradation of outer membrane protein A in Escherichia coli killing by neutrophil elastase | journal = Science | volume = 289 | issue = 5482 | pages = 1185–8 | date = August 2000 | pmid = 10947984 | doi = 10.1126/science.289.5482.1185 }}
2. ^{{cite journal | vauthors = Thomas MP, Whangbo J, McCrossan G, Deutsch AJ, Martinod K, Walch M, Lieberman J | title = Leukocyte protease binding to nucleic acids promotes nuclear localization and cleavage of nucleic acid binding proteins | journal = J. Immunol. | volume = 192 | issue = 11 | pages = 5390–7 | date = June 2014 | pmid = 24771851 | pmc = 4041364 | doi = 10.4049/jimmunol.1303296 }}
3. ^{{cite journal | vauthors = Takahashi H, Nukiwa T, Yoshimura K, Quick CD, States DJ, Holmes MD, Whang-Peng J, Knutsen T, Crystal RG | title = Structure of the human neutrophil elastase gene | journal = J. Biol. Chem. | volume = 263 | issue = 29 | pages = 14739–47 | date = October 1988 | pmid = 2902087 | doi = | url = http://www.jbc.org/cgi/reprint/263/29/14739 }}
4. ^{{cite journal | vauthors = Weinrauch Y, Drujan D, Shapiro SD, Weiss J, Zychlinsky A | title = Neutrophil elastase targets virulence factors of enterobacteria | journal = Nature | volume = 417 | issue = 6884 | pages = 91–4 | date = May 2002 | pmid = 12018205 | doi = 10.1038/417091a }}
5. ^{{cite web | title = Entrez Gene: ELA2 elastase 2, neutrophil| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=1991| accessdate = }}
6. ^{{cite journal | vauthors = Dale DC, Link DC | title = The many causes of severe congenital neutropenia | journal = N. Engl. J. Med. | volume = 360 | issue = 1 | pages = 3–5 | date = January 2009 | pmid = 19118300 | pmc = 4162527 | doi = 10.1056/NEJMp0806821 }}
7. ^{{cite journal | vauthors = Korkmaz B, Horwitz MS, Jenne DE, Gauthier F | title = Neutrophil elastase, proteinase 3, and cathepsin G as therapeutic targets in human diseases | journal = Pharmacol. Rev. | volume = 4 | issue = 62 | pages = 726–59 | date = December 2010 | pmid = 21079042 | doi=10.1124/pr.110.002733 | pmc=2993259}}
8. ^{{cite journal | vauthors = Brower MS, Harpel PC | title = Proteolytic cleavage and inactivation of alpha 2-plasmin inhibitor and C1 inactivator by human polymorphonuclear leukocyte elastase | journal = J. Biol. Chem. | volume = 257 | issue = 16 | pages = 9849–54 | date = August 1982 | pmid = 6980881 }}
9. ^{{cite journal | vauthors = Shieh BH, Travis J | title = The reactive site of human alpha 2-antiplasmin | journal = J. Biol. Chem. | volume = 262 | issue = 13 | pages = 6055–9 | date = May 1987 | pmid = 2437112 }}

Further reading

{{refbegin | 2}}
  • {{cite journal | vauthors = Dale DC, Liles WC, Garwicz D, Aprikyan AG | title = Clinical implications of mutations of neutrophil elastase in congenital and cyclic neutropenia | journal = J. Pediatr. Hematol. Oncol. | volume = 23 | issue = 4 | pages = 208–10 | year = 2001 | pmid = 11846296 | doi = 10.1097/00043426-200105000-00005 }}
  • {{cite journal | vauthors = Horwitz M, Benson KF, Duan Z, Person RE, Wechsler J, Williams K, Albani D, Li FQ | title = Role of neutrophil elastase in bone marrow failure syndromes: molecular genetic revival of the chalone hypothesis | journal = Curr. Opin. Hematol. | volume = 10 | issue = 1 | pages = 49–54 | year = 2003 | pmid = 12483111 | doi = 10.1097/00062752-200301000-00008 }}
  • {{cite journal | vauthors = Ancliff PJ, Gale RE, Linch DC | title = Neutrophil elastase mutations in congenital neutropenia | journal = Hematology | volume = 8 | issue = 3 | pages = 165–71 | year = 2003 | pmid = 12745650 | doi = 10.1080/1024533031000107497 }}
  • {{cite journal | vauthors = Horwitz M, Benson KF, Duan Z, Li FQ, Person RE | title = Hereditary neutropenia: dogs explain human neutrophil elastase mutations | journal = Trends Mol Med | volume = 10 | issue = 4 | pages = 163–70 | year = 2004 | pmid = 15059607 | doi = 10.1016/j.molmed.2004.02.002 }}
{{refend}}

External links

  • [https://www.ncbi.nlm.nih.gov/books/NBK1533/ GeneReviews/NCBI/NIH/UW entry on ELANE-Related Neutropenias]
  • {{MeshName|Neutrophil+Elastase}}
{{PDB Gallery|geneid=1991}}{{Serine endopeptidases}}{{Enzymes}}{{Portal bar|Molecular and Cellular Biology|border=no}}

2 : EC 3.4.21|Extracellular matrix remodeling enzymes

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