Chemokines (), or chemotactic cytokines, are a family of small or Cell signaling secreted by cells that induce directional movement of leukocytes, as well as other cell types, including Endothelium and Epithelium cells.
Cytokine proteins are classified as chemokines according to behavior and structural characteristics. In addition to being known for mediating chemotaxis, chemokines are all approximately 8–10 in mass and have four cysteine residues in conserved locations that are key to forming their 3-dimensional shape.
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-inflammation and can be induced during an immune response to recruit 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 , some and some bacteria, but none have been found in other .
Chemokines have been classified into four main subfamilies: CXC, CC, CX3C and C. All of 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.
Function
[[Image:Chemokine concentration chemotaxis.svg|thumb|right|300px|
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 act as a chemoattractant 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
to the
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 cells. Some chemokines have roles in development; they promote
angiogenesis (the growth of new
), or guide cells to tissues that provide specific signals critical for cellular maturation. Other chemokines are
inflammation and are released from a wide variety of cells in response to
infection,
and agents that cause physical damage such as
silica or the
Uric acid that occur in
gout. Their release is often stimulated by pro-inflammatory cytokines such as interleukin 1. Inflammatory chemokines function mainly as chemoattractants for
, recruiting
,
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.
Types by function
Chemokines are functionally divided into two groups:
-
Homeostatic: are constitutively produced in certain tissues and are responsible for basal leukocyte migration. These include: CCL14, CCL19, CCL20, CCL21, CCL25, CCL27, CXCL12 and CXCL13. This classification is not strict; for example, CCL20 can act also as pro-inflammatory chemokine.
-
Inflammatory: these are formed under pathological conditions (on pro-inflammatory stimuli, such as IL-1, TNF-alpha, LPS, or ) and actively participate in the inflammatory response attracting immune cells to the site of inflammation. Examples are: CXCL-8, CCL2, CCL3, CCL4, CCL5, CCL11, CXCL10.
Homing
The main function of chemokines is to manage the migration of
leukocytes (homing) in the respective anatomical locations in inflammatory and
homeostatic processes.
Basal: homeostatic chemokines are basal produced in the thymus and lymphoid tissues. Their homeostatic function in homing is best exemplified by the chemokines CCL19 and CCL21 (expressed within lymph nodes and on lymphatic endothelial cells) and their receptor CCR7 (expressed on cells destined for homing in cells to these organs). Using these is possible routing antigen-presenting cells (APC) to lymph nodes during the adaptive immune response. Among other homeostatic chemokine receptors include: CCR9, CCR10, and CXCR5, which are important as part of the cell addresses for tissue-specific homing of leukocytes. CCR9 supports the migration of leukocytes into the intestine, CCR10 to the skin and CXCR5 supports the migration of B-cell to follicles of lymph nodes. As well CXCL12 (SDF-1) constitutively produced in the bone marrow promotes proliferation of progenitor B cells in the bone marrow microenvironment.
Inflammatory: inflammation chemokines are produced in high concentrations during infection or injury and determine the migration of inflammatory leukocytes into the damaged area. Typical inflammatory chemokines include: CCL2, CCL3 and CCL5, CXCL1, CXCL2 and CXCL8. A typical example is CXCL-8, which acts as a chemoattractant for neutrophils. In contrast to the homeostatic chemokine receptors, there is significant promiscuity (redundancy) associated with binding receptor and inflammatory chemokines. This often complicates research on receptor-specific therapeutics in this area.
Types by cell attracted
-
/ : the key chemokines that attract these cells to the site of inflammation include: CCL2, CCL3, CCL5, CCL7, CCL8, CCL13, CCL17 and CCL22.
-
: the four key chemokines that are involved in the recruitment of T lymphocytes to the site of inflammation are: CCL2, CCL1, CCL22 and CCL17. Furthermore, CXCR3 expression by T-cells is induced following T-cell activation and activated T-cells are attracted to sites of inflammation where the IFN-y inducible chemokines CXCL9, CXCL10 and CXCL11 are secreted.
-
: on their surface express several receptors for chemokines: CCR1, CCR2, CCR3, CCR4, CCR5, CXCR2, and CXCR4. of these receptors CCL2 and CCL5 play an important role in mast cell recruitment and activation in the lung. There is also evidence that CXCL8 might be inhibitory of mast cells.
-
: the migration of eosinophils into various tissues involved several chemokines of CC family: CCL11, CCL24, CCL26, CCL5, CCL7, CCL13, and CCL3. Chemokines CCL11 (eotaxin) and CCL5 (RANTES) acts through a specific receptor CCR3 on the surface of eosinophils, and eotaxin plays an essential role in the initial recruitment of eosinophils into the lesion.
-
: are regulated primarily by CXC chemokines. An example CXCL8 (IL-8) is chemoattractant for neutrophils and also activating their metabolic and degranulation.
Structural characteristics
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, optimally designed to ensure efficient communications.
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
that are important for creating their 3-dimensional or tertiary structure, such as (in most cases) four
that interact with each other in pairs to create a Greek key shape that is a characteristic of chemokines. Intramolecular
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 3
10-helix, three
beta strand and a C-terminal
Alpha 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.
Types by structure
|
| |
|
|
| |
| P13500 |
| P10147 |
| P13236 |
| P13501 |
| P27784 |
| P80098 |
| P80075 |
| P51670 |
| P51671 |
| Q62401 |
| Q99616 |
| Q16627 |
| Q16663 |
| O15467 |
| Q92583 |
| P55774 |
| Q99731 |
| P78556 |
| O00585 |
| O00626 |
| P55773 |
| O00175 |
| O15444 |
| Q9Y258 |
| Q9Y4X3 |
| Q9NRJ3 |
|
|
| P09341 |
| P19875 |
| P19876 |
| P02776 |
| P42830 |
| P80162 |
| P02775 |
| P10145 |
| Q07325 |
| P02778 |
| O14625 |
| P48061 |
| O43927 |
| O95715 |
| Q9WVL7 |
| Q9H2A7 |
| Q6UXB2 |
|
|
| P47992 |
| Q9UBD3 |
|
|
| P78423 |
Members of the chemokine family are divided into four groups depending on the spacing of their first two cysteine residues. Thus the nomenclature for chemokines is, e.g.: CCL1 for the ligand 1 of the CC-family of chemokines, and CCR1 for its respective receptor.
CC chemokines
The CC chemokine (or
β-chemokine) proteins have two adjacent cysteines (
amino acids), 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.
CC chemokines induce the migration of
and other cell types such as
NK cells and
dendritic cells.
Examples of CC chemokine include monocyte chemoattractant protein-1 (MCP-1 or CCL2) which induces monocytes to leave the bloodstream and enter the surrounding tissue to become tissue .
CCL5 (or RANTES) attracts cells such as T cells, eosinophils and that express the receptor CCR5.
Increased CCL11 levels in blood plasma are associated with aging (and reduced neurogenesis) in mice and humans.
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
, 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.
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).
CX3C chemokines
A fourth group has also been discovered and members have three amino acids between the two cysteines and is termed CX
3C chemokine (or d-chemokines). The only CX
3C chemokine discovered to date is called
fractalkine (or CX
3CL1). 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.
Receptors
Chemokine receptors are G protein-coupled receptors containing 7 transmembrane domains that are found on the surface of
. 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
), 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.
Signal transduction
Chemokine receptors associate with G-proteins to transmit
Cell signaling 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
diglyceride (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
within the cell harbouring the chemokine receptor.
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,
and that sustained delivery of such inhibitors have the capacity of long-term infection control.
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.
See also
External links
