Chemokine

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Solution structure of interleukin-8, a chemokine of the CXC subfamily

Chemokines are a family of small cytokines, or proteins secreted by cells. Proteins are classified as chemokines according to shared structural characteristics such as small size (they are all approximately 8-10 kilodaltons in size), and the presence of four cysteine residues in conserved locations that are key to forming their 3-dimensional shape. Their name is derived from their ability to induce directed chemotaxis in nearby responsive cells; they are chemotactic cytokines. However, these proteins have historically been known under several other names including the 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 to promote cells of the immune system to a site of infection, while others are considered homeostatic and are involved in controlling the migration of cells during normal processes of tissue maintenance or development. Chemokines are found in all vertebrates, some viruses and some bacteria, but none have been described for other invertebrates. These proteins exert their biological effects by interacting with G protein-linked transmembrane receptors called chemokine receptors, that are selectively found on the surfaces of their target cells.

[edit] Function

Chemokines released by infected or damaged cells form a concentration gradient. Attracted cells move through the gradient towards the higher concentration of chemokine.

The major role of chemokines is to guide the migration of cells. Cells that are attracted by chemokines follow a signal of increasing chemokine concentration towards the source of the chemokine. Some chemokines control cells of the immune system during processes of immune surveillance, such as directing lymphocytes to the lymph nodes so they can screen for invasion of pathogens by interacting with antigen-presenting cells residing in these tissues. These are known as homeostatic chemokines and are produced and secreted without any need to stimulate their source cell(s). Some chemokines have roles in development; they promote angiogenesis (the growth of new blood vessels), or guide cells to tissues that provide specific signals critical for cellular maturation. Other chemokines are inflammatory and 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. Their release is often stimulated by pro-inflammatory cytokines such as interleukin 1. Inflammatory chemokines function mainly as chemoattractants for leukocytes, recruiting monocytes, neutrophils and other effector cells from the blood to sites of infection or tissue damage. Certain inflammatory chemokines activate cells to initiate an immune response or promote wound healing. They are released by many different cell types and serve to guide cells of both innate immune system and adaptive immune system.

[edit] Structural characteristics

All chemokines share a typical Greek key structure that is stabilised by disulfide bonds between conserved cysteine residues.

Proteins are classified into the chemokine family based on their structural characteristics, not just their ability to attract cells. All chemokines are small, with a molecular mass of between 8 and 10 kDa. They are approximately 20-50% identical to each other; that is, they share gene sequence and amino acid sequence homology. They all also possess conserved amino acids that are important for creating their 3-dimensional or tertiary structure, such as (in most cases) four cysteines that interact with each other in pairs to create a Greek key shape that is a characteristic of chemokines. Intramolecular disulfide bonds typically join the first to third, and the second to fourth cysteine residues, numbered as they appear in the protein sequence of the chemokine. Typical chemokine proteins are produced as pro-peptides, beginning with a signal peptide of approximately 20 amino acids that gets cleaved from the active (mature) portion of the molecule during the process of its secretion from the cell. The first two cysteines, in a chemokine, are situated close together near the N-terminal end of the mature protein, with the third cysteine residing in the centre of the molecule and the fourth close to the C-terminal end. A loop of approximately ten amino acids follows the first two cysteines and is known as the N-loop. This is followed by a single-turn helix, called a 3₁₀-helix, three β-strands and a C-terminal α-helix. These helices and strands are connected by turns called 30s, 40s and 50s loops; the third and fourth cysteines are located in the 30s and 50s loops.^[1]

[edit] Types

CC chemokines
Name	Gene	Other name(s)	Uniprot
CCL1	Scya1	I-309, TCA-3	P22362
CCL2	Scya2	MCP-1	P13500
CCL3	Scya3	MIP-1α	P10147
CCL4	Scya4	MIP-1β	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-1γ	P51670
CCL11	Scya11	Eotaxin	P51671
CCL12	Scya12	MCP-5	Q62401
CCL13	Scya13	MCP-4, NCC-1, Ckβ10	Q99616
CCL14	Scya14	HCC-1, MCIF, Ckβ1, NCC-2, CCL	Q16627
CCL15	Scya15	Leukotactin-1, MIP-5, HCC-2, NCC-3	Q16663
CCL16	Scya16	LEC, NCC-4, LMC, Ckβ12	O15467
CCL17	Scya17	TARC, dendrokine, ABCD-2	Q92583
CCL18	Scya18	PARC, DC-CK1, AMAC-1, Ckβ7, MIP-4	P55774
CCL19	Scya19	ELC, Exodus-3, Ckβ11	Q99731
CCL20	Scya20	LARC, Exodus-1, Ckβ4	P78556
CCL21	Scya21	SLC, 6Ckine, Exodus-2, Ckβ9, TCA-4	O00585
CCL22	Scya22	MDC, DC/β-CK	O00626
CCL23	Scya23	MPIF-1, Ckβ8, MIP-3, MPIF-1	P55773
CCL24	Scya24	Eotaxin-2, MPIF-2, Ckβ6	O00175
CCL25	Scya25	TECK, Ckβ15	O15444
CCL26	Scya26	Eotaxin-3, MIP-4α, IMAC, TSC-1	Q9Y258
CCL27	Scya27	CTACK, ILC, Eskine, PESKY, skinkine	Q9Y4X3
CCL28	Scya28	MEC	Q9NRJ3
CXC chemokines
Name	Gene	Other name(s)	Uniprot
CXCL1	Scyb1	Gro-α, GRO1, NAP-3	P09341
CXCL2	Scyb2	Gro-β, GRO2, MIP-2α	P19875
CXCL3	Scyb3	Gro-γ, GRO3, MIP-2β	P19876
CXCL4	Scyb4	PF-4	P02776
CXCL5	Scyb5	ENA-78	P42830
CXCL6	Scyb6	GCP-2	P80162
CXCL7	Scyb7	NAP-2, CTAPIII, β-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, β-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
C chemokines
Name	Gene	Other name(s)	Uniprot
XCL1	Scyc1	Lymphotactin α, SCM-1α, ATAC	P47992
XCL2	Scyc2	Lymphotactin β, SCM-1β	Q9UBD3
CX3C chemokines
Name	Gene	Other name(s)	Uniprot
CX3CL1	Scyd1	Fractalkine, Neurotactin, ABCD-3	P78423

Members of the chemokine family are categorized into four groups depending on the spacing of their first two cysteine residues.

[edit] CC chemokines

The CC chemokines (or β-chemokines) have two adjacent cysteines near their amino terminus. There have been at least 27 distinct members of this subgroup reported for mammals, called CC chemokine ligands (CCL)-1 to -28; CCL10 is the same as CCL9. Chemokines of this subfamily usually contain four cysteines (C4-CC chemokines), but a small number of CC chemokines possess six cysteines (C6-CC chemokines). C6-CC chemokines include CCL1, CCL15, CCL21, CCL23 and CCL28.^[2] 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 or CCL2) which induces monocytes to leave the bloodstream and enter the surrounding tissue to become tissue macrophages. CC chemokines induce cellular migration by binding to and activating CC chemokine receptors, ten of which have been discovered to date and called CCR1-10. These receptors are expressed on the surface of different cell types allowing their specific attraction by the chemokines. A CC chemokine that attracts lymphocytes is CCL28, which is chemoattractant to T cells and B cells that express the chemokine receptor CCR10. This chemokine can also attract eosinophils that express CCR3. CCL5 (or RANTES) attracts cells such as T cells, eosinophils and basophils that express the receptor CCR5.

[edit] CXC chemokines

The two N-terminal cysteines of CXC chemokines (or α-chemokines) are separated by one amino acid, represented in this name with an "X". There have been 17 different CXC chemokines described in mammals, that are subdivided into two categories, those with a specific amino acid sequence (or motif) of Glutamic acid-Leucine-Arginine (or ELR for short) immediately before the first cysteine of the CXC motif (ELR-positive), and those without an ELR motif (ELR-negative). ELR-positive CXC chemokines specifically induce the migration of neutrophils, and interact with chemokine receptors CXCR1 and CXCR2. An example of an ELR-positive CXC chemokine is interleukin-8 (IL-8), which induces neutrophils to leave the bloodstream and enter into the surrounding tissue. Other CXC chemokines that lack the ELR motif, such as CXCL13, tend to be chemoattractant for lymphocytes. CXC chemokines bind to CXC chemokine receptors, of which seven have been discovered to date, designated CXCR1-7.

[edit] C chemokines

The third group of chemokines is known as the C chemokines (or γ chemokines), and is unlike all other chemokines in that it has only two cysteines; one N-terminal cysteine and one cysteine downstream. Two chemokines have been described for this subgroup and are called XCL1 (lymphotactin-α) and XCL2 (lymphotactin-β). These chemokines attract T cell precursors to the thymus.

[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] Receptors

For more details on this topic, see Chemokine receptor.

[edit] Structure and Features

Chemokine receptors are G protein-coupled receptors containing 7 transmembrane domains that are found on the surface of leukocytes. Approximately 19 different chemokine receptors have been characterized to date, which are divided into four families depending on the type of chemokine they bind; CXCR that bind CXC chemokines, CCR that bind CC chemokines, CX3CR1 that binds the sole CX3C chemokine (CX3CL1), and XCR1 that binds the two XC chemokines (XCL1 and XCL2). They share many structural features; they are similar in size (with about 350 amino acids), have a short, acidic N-terminal end, seven helical transmembrane domains with three intracellular and three extracellular hydrophilic loops, and an intracellular C-terminus containing serine and threonine residues important for receptor regulation. The first two extracellular loops of chemokine receptors each has a conserved cysteine residue that allow formation of a disulfide bridge between these loops. G proteins are coupled to the C-terminal end of the chemokine receptor to allow intracellular signaling after receptor activation, while the N-terminal domain of the chemokine receptor determines ligand binding specificity.^[3]

[edit] Signal Transduction

Chemokine receptors associate with G-proteins to transmit cell signals following ligand binding. Activation of G proteins, by chemokine receptors, causes the subsequent activation of an enzyme known as phospholipase C (PLC). PLC cleaves a molecule called Phosphatidylinositol (4,5)-bisphosphate (PIP2) into two second messenger molecules known as Inositol triphosphate (IP3) and diacylglycerol (DAG) that trigger intracellular signaling events; DAG activates another enzyme called protein kinase C (PKC), and IP3 triggers the release of calcium from intracellular stores. These events promote many signaling cascades (such as the MAP kinase pathway) that generate responses like chemotaxis, degranulation, release of superoxide anions and changes in the avidity of cell adhesion molecules called integrins within the cell harbouring the chemokine receptor.^[4]

[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.^[5] 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.^[6]

[edit] External links

• IUPHAR GPCR Database - Chemokine Receptors
• List of chemokines and their receptors at nlm.nih.gov
• The cytokine family database - Chemokines at kumamoto-u.ac.jp
• The correct chemokine nomenclature at rndsystems.com

[edit] See also

• Paracrine signalling

[edit] References

1. ^ Fernandez E, Lolis E. "Structure, function, and inhibition of chemokines". Annu Rev Pharmacol Toxicol 42: 469-99. PMID 11807180. 
2. ^ Laing K, Secombes C (2004). "Chemokines". Dev Comp Immunol 28 (5): 443-60. PMID 15062643. 
3. ^ Craig Murdoch and Adam Finn (2000). "Chemokine receptors and the role in inflammation and infectious disease". Journal of the American Society of Hematology 95 (10): 3032-3043. 
4. ^ Craig Murdoch and Adam Finn (2000). "Chemokine receptors and the role in inflammation and infectious disease". Journal of the American Society of Hematology 95 (10): 3032-3043. 
5. ^ 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. 
6. ^ 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.