| First Author | Westermann LM | Year | 2020 |
| Journal | Dis Model Mech | Volume | 13 |
| Issue | 11 | PubMed ID | 33023972 |
| Mgi Jnum | J:298718 | Mgi Id | MGI:6477261 |
| Doi | 10.1242/dmm.046425 | Citation | Westermann LM, et al. (2020) Imbalanced cellular metabolism compromises cartilage homeostasis and joint function in a mouse model of mucolipidosis type III gamma. Dis Model Mech :dmm046425 |
| abstractText | Mucolipidosis type III (MLIII) gamma is a rare inherited lysosomal storage disorder caused by mutations in GNPTG encoding the gamma-subunit of GlcNAc-1-phosphotransferase, the key enzyme ensuring proper intracellular location of multiple lysosomal enzymes. Patients with MLIII gamma typically present with osteoarthritis and joint stiffness, suggesting cartilage involvement. Using Gnptg (ko) mice as a model of the human disease, we showed that missorting of a number of lysosomal enzymes is associated with intracellular accumulation of chondroitin sulfate in Gnptg (ko) chondrocytes and their impaired differentiation, as well as with an altered microstructure of the cartilage extracellular matrix (ECM). We also demonstrated distinct functional and structural properties of the Achilles tendons isolated from Gnptg (ko) and Gnptab (ki) mice, the latter displaying a more severe phenotype resembling mucolipidosis type II (MLII) in humans. Together with comparative analyses of joint mobility in MLII and MLIII patients, these findings provide a basis for better understanding of the molecular reasons leading to joint pathology in these patients. Our data suggest that lack of GlcNAc-1-phosphotransferase activity due to defects in the gamma-subunit causes structural changes within the ECM of connective and mechanosensitive tissues, such as cartilage and tendon, and eventually results in functional joint abnormalities typically observed in MLIII gamma patients. This idea was supported by a deficit of the limb motor function in Gnptg (ko) mice challenged on a Rotarod under fatigue-associated conditions, suggesting that the impaired motor performance of Gnptg (ko) mice was caused by fatigue and/or pain at the joint. |
