Aggrecan

ACAN
Available structures PDB Ortholog search: PDBe RCSB List of PDB id codes 4MD4
Identifiers
Aliases	ACAN, AGC1, AGCAN, CSPG1, CSPGCP, MSK16, SEDK, Aggrecan, SSOAOD
External IDs	OMIM: 155760; MGI: 99602; HomoloGene: 136177; GeneCards: ACAN; OMA:ACAN - orthologs
Gene location (Human) Chr. Chromosome 15 (human)[1] Band 15q26.1 Start 88,803,436 bp[1] End 88,875,353 bp[1]
Gene location (Mouse) Chr. Chromosome 7 (mouse)[2] Band 7 D2|7 44.88 cM Start 78,703,231 bp[2] End 78,764,847 bp[2]
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in tibia popliteal artery ascending aorta middle frontal gyrus trachea Achilles tendon right coronary artery periodontal fiber trabecular bone pancreatic ductal cell Top expressed in fossa condyle intercostal muscle trachea ascending aorta ankle aortic valve body of femur motor neuron calvaria More reference expression data BioGPS More reference expression data
Gene ontology Molecular function extracellular matrix structural constituent metal ion binding protein binding hyaluronic acid binding carbohydrate binding extracellular matrix structural constituent conferring compression resistance Cellular component extracellular matrix extracellular region lysosomal lumen Golgi lumen basement membrane collagen-containing extracellular matrix perisynaptic extracellular matrix glutamatergic synapse GABA-ergic synapse Biological process skeletal system development extracellular matrix disassembly extracellular matrix organization proteolysis central nervous system development keratan sulfate catabolic process keratan sulfate biosynthetic process cell adhesion cartilage condensation chondrocyte development heart development proteoglycan biosynthetic process collagen fibril organization Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 176 11595 Ensembl ENSG00000157766 ENSMUSG00000030607 UniProt P16112 Q61282 RefSeq (mRNA) NM_001135 NM_013227 NM_001369268 NM_007424 NM_001361500 RefSeq (protein) NP_001126 NP_037359 NP_001356197 NP_031450 NP_001348429 Location (UCSC) Chr 15: 88.8 – 88.88 Mb Chr 7: 78.7 – 78.76 Mb PubMed search [3] [4]
Wikidata
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Aggrecan (ACAN), also known as cartilage-specific proteoglycan core protein (CSPCP) or chondroitin sulfate proteoglycan 1, is a protein that in humans is encoded by the ACAN gene.^[5] This gene is a member of the lectican (chondroitin sulfate proteoglycan) family. The encoded protein is an integral part of the extracellular matrix in cartilagenous tissue and it withstands compression in cartilage.

Aggrecan is a proteoglycan, or a protein modified with large carbohydrates; the human form of the protein is 2316 amino acids long and can be expressed in multiple isoforms due to alternative splicing.^[5] Aggrecan was named for its ability to form large aggregates in the cartilage tissue (a large aggregating proteoglycan).^{[6] [7]}

Structure

Aggrecan is a high molecular weight (1x10⁶ < M < 3x10⁶) proteoglycan. It exhibits a bottlebrush structure, in which chondroitin sulfate and keratan sulfate glycosaminoglycan (GAG) chains are attached to an extended protein core.^[8]

Aggrecan has a molecular mass >2,500 kDa.^[9] The core protein (~300 kDa^[10]) has around 100 GAG chains attached to it.^[11]

Aggrecan consists of two globular structural domains (G1 and G2) at the N-terminal end and one globular domain (G3) at the C-terminal end, separated by a large extended domain (CS) heavily modified with GAGs. (N-G1-G2-CS-G3-C) The two main modifier moieties are themselves arranged into distinct regions, a chondroitin sulfate and a keratan sulfate region.

The three globular domains, G1, G2, and G3 are involved in aggregation, hyaluronan binding, cell adhesion, and chondrocyte apoptosis.

Recent molecular simulations and neutron scattering experiments suggested that aggrecan in aqueous solutions forms two-dimensional aggregates that resemble sheet-like shapes.^[7]

Along with type-II collagen, aggrecan forms a major structural component of cartilage, particularly articular cartilage.

The aggrecan family includes other important members such as versican, also named PG-M, neurocan, brevican and the cell surface HA receptor CD44. They are modular proteoglycans containing combinations of structural motifs, such as EGF-like domains, carbohydrate recognition domains (CRD), complement binding protein (CBP)-like domains, immunoglobulin folds and proteoglycan tandem repeats.

Function

Aggrecan is a critical component for cartilage structure and the function of joints.

Functionally, the G1 domain interacts with hyaluronic acid and link protein, forming stable ternary complexes in the extracellular matrix. G2 is homologous to the tandem repeats of G1 and of link protein and is involved in product processing. G3 makes up the carboxyl terminus of the core protein. It enhances glycosaminoglycan modification and product secretion. Aggrecan plays an important role in mediating chondrocyte-chondrocyte and chondrocyte-matrix interactions through its ability to bind hyaluronan.^[11]

Aggrecan provides intervertebral disc and cartilage with the ability to resist compressive loads. The localized high concentrations of aggrecan provide the osmotic properties necessary for normal tissue function with the GAGs producing the swelling pressure that counters compressive loads on the tissue. This functional ability is dependent on a high GAG/aggrecan concentration being present in the tissue extracellular matrix.^[12] In the disc, aggrecan concentrations peak in a person's twenties, and decline thereafter, with aggrecan degradation products slowly accumulating over the following decades.^[13] This causes discs to get stiffer and less resilient with age.

Aggrecan also plays an important role in the organization of the extracellular spaces between neurons in the brain.^[14] Through interactions with link protein and tenascins, aggrecan binds to hyaluronan, forming large aggregated complexes at the cell surface.

Clinical significance

The synthesis and degradation of aggrecan are being investigated for their roles in cartilage deterioration during joint injury, disease, and aging.

The linker domain between the N-terminal globular domains, called the interglobular domain, is highly sensitive to proteolysis. Such degradation has been associated with the development of arthritis. Proteases capable of degrading aggrecans are called aggrecanases, and they are members of the ADAM (A Disintegrin And Metalloprotease) protein family.^[15]

Degenerative joint disease is a leading source of morbidity resulting in significant social and economic impact. Osteoarthritis is characterized by the slow progressive deterioration of articular cartilage and fibrosis of the synovium and joint capsule. Articular cartilage contains up to 10% proteoglycan by weight, most of which is aggrecan, and its loss is an early sign of the disease.

References

Further reading

External links

• Aggrecan at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
• Human ACAN genome location and ACAN gene details page in the UCSC Genome Browser.
• Overview of all the structural information available in the PDB for UniProt: P16112 (Human Aggrecan core protein) at the PDBe-KB.
• Overview of all the structural information available in the PDB for UniProt: P07897 (Rat Aggrecan core protein) at the PDBe-KB.