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Chemokine

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Chemokines are a family of small cytokines, or proteins secreted by cells. Chemokines induce directed chemotaxis in nearby responsive cells, hence the name chemotactic cytokines. Former names for these proteins include SIS family of cytokines, SIG family of cytokines, SCY family of cytokines, Platelet factor-4 superfamily or intercrines. Some chemokines are considered pro-inflammatory and can be induced during an immune response while others are considered homeostatic.

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[edit] Characteristics

All chemokines have molecular masses of between 8 and 10 kDa and are approximately 20-50% identical. That is, they share 20-50% gene sequence and amino acid sequence homology with each other. Their receptors are all integral membrane proteins containing seven membrane-spanning helices which are coupled to G proteins. The proteins also share common tertiary structures. All chemokines possess a number of conserved cysteine residues involved in intramolecular disulfide bond formation.

[edit] Function

Inflammatory chemokines are released from a wide variety of cells in response to bacterial infection, viruses and agents that cause physical damage such as silica or the urate crystals that occur in gout. They function mainly as chemoattractants for leukocytes, recruiting monocytes, neutrophils and other effector cells from the blood to sites of infection or damage. They can be released by many different cell types and serve to guide cells involved in innate immunity and also the lymphocytes of the adaptive immune system. Some chemokines also have roles in the development of lymphocytes, migration and angiogenesis (the growth of new blood vessels).

[edit] Types

Members of the chemokine family are categorized into four groups: The CC chemokines (or β-chemokines) with two adjacent cysteines near the amino terminus of the protein, and CXC chemokines (or α-chemokines) in which the cysteines are separated by an amino acid, the CX3C chemokines (or δ chemokines) and the C chemokines (or γ chemokines). The four groups of chemokines act on different receptors.

[edit] CC chemokines

CC chemokines bind to CC chemokine receptors, of which ten have been discovered to date, designated CCR1-10. These receptors are expressed on the surface of different cell types allowing their specific attraction by the chemokines.

CC chemokines induce the migration of monocytes and other cell types such as NK cells and dendritic cells. An example of a CC chemokine is monocyte chemoattractant protein-1 (MCP-1) which induces monocytes to leave the bloodstream and enter the surrounding tissue, becoming tissue macrophages. CCL28 attracts T cells and B cells that express CCR10, and eosinophils that express CCR3. It has also been implicated in anti-microbial activity. CCR5, or chemokine (C-C motif) receptor 5, binds RANTES/CCL5.

[edit] CXC chemokines

CXC chemokines which have a specific amino acid sequence (or motif) of Glutamic acid-Leucine-Arginine (or ELR for short) immediately before the first cysteine induce the migration of neutrophils. An example of this is interleukin-8 (IL-8) which induces neutrophils to leave the bloodstream and enter into the surrounding tissue. Other CXC chemokines which lack the ELR motif, such as the B-lymphocyte chemokine (BLC) are chemoattractant for lymphocytes. CXC chemokines bind to CXC chemokine receptors, of which seven have been discovered to date, designated CXCR1-7. CXCR4 is involved in HIV infection.

[edit] C chemokines

The only known chemokine with only one cysteine is lymphotactin and is thought to attract T cell precursors to the thymus. Its family is known as the C chemokines (or γ-chemokines).

[edit] CX3C chemokines

A fourth group has also been discovered and members have three amino acids between the two cysteines and is termed CX3C chemokine (or δ-chemokines). The only CX3C chemokine discovered to date is called fractalkine (or CX3CL1). It is both secreted and tethered to the surface of the cell that expresses it, thereby serving as both a chemoattractant and as an adhesion molecule.

[edit] Infection control

The discovery that the β chemokines RANTES, MIP (Macrophage Inflammatory Proteins) 1α and 1β (now known as CCL5, CCL3 and CCL4 respectively) suppress HIV-1 provided the initial connection and indicated that these molecules might control infection as part of immune responses in vivo.[1] The association of chemokine production with antigen-induced proliferative responses, more favorable clinical status in HIV infection, as well as with an uninfected status in subjects at risk for infection suggests a positive role for these molecules in controlling the natural course of HIV infection.[2]

[edit] External links

[edit] See also

[edit] Further reading

  1.   Cocchi F, DeVico AL, Garzino-Demo A, Arya SK, Gallo RC, and Lusso P (October 1995). "Identification of RANTES, MIP-1a, and MIP-1b as the major HIV-suppressive factor produced by CD8+ T cells". Science 270: 1811-1815.
  2.   Alfredo Garzino-Demo, Ronald B. Moss, Joseph B. Margolick, Farley Cleghorn, Anne Sill, William A. Blattner, Fiorenza Cocchi, Dennis J. Carlo, Anthony L. DeVico, and Robert C. Gallo (October 1999). "Spontaneous and antigen-induced production of HIV-inhibitory β-chemokines are associated with AIDS-free status". Proc Natl Acad Sci U S A 96 (21): 11986–11991.
  3. Ransohoff, Richard, et al. (2002). Universes in Delicate Balance: Chemokines and the Nervous System. Elsevier. ISBN 044430028.
  4. Laing KJ & Secombes CJ (2004). "Chemokines". Developmental and Comparative Immunology 28: 443-460.
Mammalian CXC chemokines
Official name Gene name Other name(s) Uniprot ID
CXCL1 Scyb1 Gro-alpha, GRO1, NAP-3 P09341
CXCL2 Scyb2 Gro-beta, GRO2, MIP-2a P19875
CXCL3 Scyb3 Gro-gamma, GRO3, MIP-2beta P19876
CXCL4 Scyb4 PF-4 P02776
CXCL5 Scyb5 ENA-78 P42830
CXCL6 Scyb6 GCP-2 P80162
CXCL7 Scyb7 NAP-2, CTAPIII, beta-Ta, PEP P02775
CXCL8 Scyb8 IL-8, NAP-1, MDNCF, GCP-1 P10145
CXCL9 Scyb9 MIG, CRG-10 Q07325
CXCL10 Scyb10 IP-10, CRG-2 P02778
CXCL11 Scyb11 I-TAC, beta-R1, IP-9 O14625
CXCL12 Scyb12 SDF-1, PBSF P48061
CXCL13 Scyb13 BCA-1, BLC O43927
CXCL14 Scyb14 BRAK, bolekine O95715
CXCL15 Scyb15 Lungkine, WECHE Q9WVL7
CXCL16 Scyb16 SRPSOX Q9H2A7
CXCL17 VCC-1 DMC, VCC-1 Q6UXB2
Mammalian CC chemokines
Official name Gene name Other name(s) Uniprot ID
CCL1 Scya1 I-309, TCA-3 P22362
CCL2 Scya2 MCP-1 P13500
CCL3 Scya3 MIP-1a P10147
CCL4 Scya4 MIP-1b P13236
CCL5 Scya5 RANTES P13501
CCL6 Scya6 C10, MRP-2 P27784
CCL7 Scya7 MARC, MCP-3 P80098
CCL8 Scya8 MCP-2 P80075
CCL9/CCL10 Scya9 MRP-2, CCF18, MIP-1gamma P51670
CCL11 Scya11 Eotaxin P51671
CCL12 Scya12 MCP-5 Q62401
CCL13 Scya13 MCP-4, NCC-1, Ckbeta10 Q99616
CCL14 Scya14 HCC-1, MCIF, Ckbeta1, NCC-2, CCL Q16627
CCL15 Scya15 Leukotactin-1, MIP-5, HCC-2, NCC-3 Q16663
CCL16 Scya16 LEC, NCC-4, LMC, Ckbeta12 O15467
CCL17 Scya17 TARC, dendrokine, ABCD-2 Q92583
CCL18 Scya18 PARC, DC-CK1, AMAC-1, Ckbeta7, MIP-4 P55774
CCL19 Scya19 ELC, Exodus-3, Ckbeta11 Q99731
CCL20 Scya20 LARC, Exodus-1, Ckbeta4 P78556
CCL21 Scya21 SLC, 6Ckine, Exodus-2, Ckbeta9, TCA-4 O00585
CCL22 Scya22 MDC, DC/beta-CK O00626
CCL23 Scya23 MPIF-1, Ckbeta8, MIP-3, MPIF-1 P55773
CCL24 Scya24 Eotaxin-2, MPIF-2, Ckbeta6 O00175
CCL25 Scya25 TECK, Ckbeta15 O15444
CCL26 Scya26 Eotaxin-3, MIP-4a, IMAC, TSC-1 Q9Y258
CCL27 Scya27 CTACK, ILC, Eskine, PESKY, skinkine Q9Y4X3
CCL28 Scya28 MEC Q9NRJ3
Mammalian C chemokines
Official name Gene name Other name(s) Uniprot ID
CL1 Scyc1 Lymphotactin alpha, SCM-1alpha, ATAC P47992
CL2 Scyc2 Lymphotactin beta, SCM-1beta Q9UBD3
Mammalian CX3C chemokines
Official name Gene name Other name(s) Uniprot ID
CX3CL1 Scyd1 Fractalkine, Neurotactin, ABCD-3 P78423
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