ACAN

Official Full Name

aggrecan

Organism

Homo sapiens

Gene ID

176

Background

This gene is a member of the aggrecan/versican proteoglycan family. The encoded protein is an integral part of the extracellular matrix in cartilagenous tissue and it withstands compression in cartilage. Mutations in this gene may be involved in skeletal dysplasia and spinal degeneration. Multiple alternatively spliced transcript variants that encode different protein isoforms have been observed in this gene. [provided by RefSeq, Jul 2008]

Synonyms

ATP12; ATP12p; LP3663; MC5DN1

Cat.No.	Product Name	Price
CSC-DC000119	Panoply™ Human ACAN Knockdown Stable Cell Line	Inquiry
CSC-SC000119	Panoply™ Human ACAN Over-expressing Stable Cell Line	Inquiry

Cat.No.	Product Name	Price
SHG028177	shRNA set against Mouse Acan(NM_007424.2)	Inquiry
SHH229974	shRNA set against Human ACAN (NM_001135.3)	Inquiry
SHH229978	shRNA set against Mouse ACAN (NM_007424.2)	Inquiry
SHH229982	shRNA set against Rat ACAN (NM_022190.1)	Inquiry
SHW005457	shRNA set against Chicken ACAN (NM_204955)	Inquiry

Cat.No.	Product Name	Price
CDCR296175	Human ACAN ORF Clone(NM_013227.3)	Inquiry
CDCR350158	Human ACAN ORF Clone(NM_001135.3)	Inquiry
CDFH000151	Human ACAN cDNA Clone(NM_001135.3)	Inquiry
CDFH000155	Human ACAN cDNA Clone(NM_013227.3)	Inquiry
CDFR011878	Rat Acan cDNA Clone(NM_022190.1)	Inquiry
MiUTR1M-01102	ACAN miRNA 3'UTR clone	Inquiry
MiUTR1R-00169	ACAN miRNA 3'UTR clone	Inquiry
MiUTR3H-01392	ACAN miRNA 3'UTR clone	Inquiry
MiUTR3H-01393	ACAN miRNA 3'UTR clone	Inquiry
CDCB166932	Chicken ACAN ORF Clone (NM_204955)	Inquiry
CDCB180502	Rabbit ACAN ORF clone (XM_008251722.1)	Inquiry
CDCL182527	Human ACAN ORF clone(NM_002203.3)	Inquiry
CDCR243292	Mouse Acan ORF Clone(NM_007424.2)	Inquiry
CDCR378881	Rat Acan ORF Clone(NM_022190.1)	Inquiry

Detailed Information

The ACAN (aggrecan)gene is located at 15q25-q26.2, which consists of 19 exons ranging in size from 77 to 4224 bp. ACAN is an important component of the extracellular matrix of the intervertebral disc nucleus, accounting for approximately 70% of the dry weight of the nucleus pulposus. Studies have shown that collectin proteoglycans are central hyaluronic acid (HA) filaments linked to ACAN and connexin (LP). The core protein domain of ACAN is a G1, G2, G3 globular region; IGD, intersphere domain; KS, a keratan sulfate-rich domain; CS1 and CS2, a chondroitin sulfate-rich domain.

In 1997, Doege et al. found that there is a variable number of tandem repeat (VNTR) polymorphisms on the 12th exon of the human ACAN gene, which means that the number of repeats of the gene fragment is different, leading to different lengths of the fragment. The ACAN gene polymorphism is actually a repeat polymorphism. This polymorphism has not been found in other species so far. The number of repeats may determine the length of the domain in the core protein, which in turn determines the number of chondroitin sulfate chains attached to it, confirming the functional characteristics of proteoglycans at the genetic and molecular levels.

For ideal tissue function, ACAN concentration, charge and size must be as large as possible. Thus, the optimal ACAN molecule achieves the largest substitution, the longest and most sulfated GAG chain through the GAG chain and forms the largest aggregate with HA. Proteoglycan aggregates are thought to be encapsulated by collagen fibers. In the relaxed state, when the anionic chondroitin sulfate and the keratan sulfate chain inhale water into the tissue, the aggregate swells until equilibrium is reached, wherein the swelling is balanced by the tension in the collagen fibers. Under compression, water is displaced and the chondroitin sulfate and keratan sulfate chains are closer, thus increasing their swelling potential and balancing the applied load. When the original balance is restored, the increased expansion potential is dissipated by the time the load is removed.

Figure 1. The function of ACAN in articular cartilage. (Roughley P J, et al. 2014)

ACAN and Degeneration of The Intervertebral Disc

With the deepening of the pathological process and molecular mechanism of intervertebral disc degeneration, the application of biological methods to intervene the degeneration process of the intervertebral disc provides a new idea for the treatment of intervertebral disc degeneration. The most important biochemical change in the early stage of ECM degeneration of the disc nucleus is the loss of proteoglycans.

Cong et al. studied 197 Han Chinese in northern China, including 70 patients with clinically symptomatic lumbar disc herniation (LDH). It was found that the ACAN content in normal human intervertebral disc tissue was significantly higher than that in the case group, while the short sequence VNTR allele expressed less ACAN. Le Maitre CL et al. have shown that increased expression of aggrecanase 1 in the nucleus pulposus cells of the intervertebral disc leads to degeneration of the intervertebral disc. Perera et al. evaluated the association of single nucleotide variants (SNVs) of the candidate genes of the ACAN metabolic pathway with the severity of lumbar disc herniation in patients with chronic mechanical low back pain. This study showed that SNVs of ACAN and their haplotypes are associated with the severity of lumbar disc herniation.

ACAN and Osteoarthritis

Because chondrocytes themselves may produce various cytokines or inflammatory synovial infiltration, and osteoarthritis has increased articular cartilage catabolism. Interleukin1 and TNFα not only stimulate the production of protease but also down regulate the production of ACAN. These inflammatory factors are related to the production of ACAN and MMPs, which reduce the ACAN core protein.

In the study of osteoarthritis, Aggrecanase 1 and 2 are the main degradation enzymes of proteoglycan, and their activity is strongly inhibited by tissue inhibitor of metalloproteinase 3 (TIMP-3). Le Maitre CL et al. showed that the increased expression of Aggrecanase 1 in the nucleus pulposus cells of the intervertebral disc could lead to degeneration of the intervertebral disc.

Ismail et al. showed that ADAMTS-5 is a major aggrecanase in human chondrocytes and is involved in the regulation of ACAN degradation by IL-1. The TRAF-6/TAK-1/MKKK-4 signal axis is required for IL-1 to induce ACAN degradation, whereas NF-Κb is not. Among the three MAPKs (ERK, p38, and JNK), only JNK-2 showed a significant effect in ACAN degradation. Chondrocytes secrete aggrecanase, which is continuously endocytosed by LRP-1, keeping the extracellular level of aggrecanase low.

Germaschewski et al. have developed a new epitope immunoassay to specifically analyze the degradation products of ACAN, whether from MMP or aggrecanase. The researchers analyzed patients with knee osteoarthritis and healthy subjects and tested the pharmacodynamic effects of the humanized monoclonal antibody ADAMTS-5 as a potential disease modifying agent for OA, which can quantify the concentration of ARGS(the degradation of ACAN by ADAMTS-5 enzyme). The detection method is more sensitive, and the measurement of the new epitope of ARGS can be used as a prognostic or stratified marker.

Reference:

Roughley P J, Mort J S. The role of aggrecan in normal and osteoarthritic cartilage. Journal of Experimental Orthopaedics, 2014, 1(1):8.
Germaschewski F M, Matheny C J, Larkin J, et al. Quantitation OF ARGS aggrecan fragments in synovial fluid, serum and urine from osteoarthritis patients. Osteoarthritis & Cartilage, 2014, 22(5):690-697.
Ismail H M, Yamamoto K, Vincent T L, et al. Interleukin-1 Acts via the JNK-2 Signaling Pathway to Induce Aggrecan Degradation by Human Chondrocytes. Arthritis Rheumatol, 2015, 67(7):1826-1836.
Sivan S S, Wachtel E, Roughley P. Structure, function, aging and turnover of aggrecan in the intervertebral disc. BBA - General Subjects, 2014, 1840(10):3181-3189.
Perera R S, Dissanayake P H, Senarath U, et al. Variants of ACAN are associated with severity of lumbar disc herniation in patients with chronic low back pain. Plos One, 2017, 12(7):e0181580.

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