PDZK1 protects against mechanical overload-induced chondrocyte senescence and osteoarthritis by targeting mitochondrial function
Yan Shao , Hongbo Zhang , Hong Guan , Chunyu Wu , Weizhong Qi , Lingfeng Yang , Jianbin Yin , Haiyan Zhang , Liangliang Liu , Yuheng Lu , Yitao Zhao , Sheng Zhang , Chun Zeng , Guiqing Wang , Xiaochun Bai , Daozhang Cai
Bone Research ›› 2024, Vol. 12 ›› Issue (1) : 41
PDZK1 protects against mechanical overload-induced chondrocyte senescence and osteoarthritis by targeting mitochondrial function
Mechanical overloading and aging are two essential factors for osteoarthritis (OA) development. Mitochondria have been identified as a mechano-transducer situated between extracellular mechanical signals and chondrocyte biology, but their roles and the associated mechanisms in mechanical stress-associated chondrocyte senescence and OA have not been elucidated. Herein, we found that PDZ domain containing 1 (PDZK1), one of the PDZ proteins, which belongs to the Na+/H+ Exchanger (NHE) regulatory factor family, is a key factor in biomechanically induced mitochondrial dysfunction and chondrocyte senescence during OA progression. PDZK1 is reduced by mechanical overload, and is diminished in the articular cartilage of OA patients, aged mice and OA mice. Pdzk1 knockout in chondrocytes exacerbates mechanical overload-induced cartilage degeneration, whereas intraarticular injection of adeno-associated virus-expressing PDZK1 had a therapeutic effect. Moreover, PDZK1 loss impaired chondrocyte mitochondrial function with accumulated damaged mitochondria, decreased mitochondrion DNA (mtDNA) content and increased reactive oxygen species (ROS) production. PDZK1 supplementation or mitoubiquinone (MitoQ) application alleviated chondrocyte senescence and cartilage degeneration and significantly protected chondrocyte mitochondrial functions. MRNA sequencing in articular cartilage from Pdzk1 knockout mice and controls showed that PDZK1 deficiency in chondrocytes interfered with mitochondrial function through inhibiting Hmgcs2 by increasing its ubiquitination. Our results suggested that PDZK1 deficiency plays a crucial role in mediating excessive mechanical load-induced chondrocyte senescence and is associated with mitochondrial dysfunction. PDZK1 overexpression or preservation of mitochondrial functions by MitoQ might present a new therapeutic approach for mechanical overload-induced OA.
| [1] |
|
| [2] |
|
| [3] |
|
| [4] |
|
| [5] |
|
| [6] |
|
| [7] |
|
| [8] |
Griffin, T. M. & Guilak, F. The role of mechanical loading in the onset and progression of osteoarthritis. Exerc. Sport Sci. Rev. 33, 195 (2005). |
| [9] |
|
| [10] |
|
| [11] |
|
| [12] |
|
| [13] |
|
| [14] |
|
| [15] |
|
| [16] |
|
| [17] |
|
| [18] |
Li, H. et al. Reprogramming macrophage polarization, depleting ROS by astaxanthin and thioketal-containing polymers delivering rapamycin for osteoarthritis treatment. Adv. Sci. (2023). |
| [19] |
|
| [20] |
|
| [21] |
|
| [22] |
|
| [23] |
|
| [24] |
Milner, P. I., Wilkins, R. J. & Gibson, J. S. The role of mitochondrial reactive oxygen species in pH regulation in articular chondrocytes. Osteoarthr. Cartil. 15, 735–742 (2007). |
| [25] |
Hopwood, B., Tsykin, A., Findlay, D. M. & Fazzalari, N. L. Microarray gene expression profiling of osteoarthritic bone suggests altered bone remodelling, WNT and transforming growth factor-beta/bone morphogenic protein signalling. Arthritis Res. Ther. 9, R100 (2007). |
| [26] |
Donowitz, M. et al. NHERF family and NHE3 regulation. J. Physiol. 567, 3–11 (2005) |
| [27] |
|
| [28] |
Chazotte, B. Labeling mitochondria with JC-1. Cold Spring Harb. Protoc. 2011, https://doi.org/10.1101/pdb.prot065490 (2011). |
| [29] |
|
| [30] |
|
| [31] |
|
| [32] |
|
| [33] |
|
| [34] |
|
| [35] |
|
| [36] |
|
| [37] |
|
| [38] |
|
| [39] |
|
| [40] |
|
National Natural Science Foundation of China (National Science Foundation of China)(82172491)
National Key Research and Development Program of China (2022YFC3601902)
State-funded postdoctoral researcher program No GZC20231062 (CN)
Youth Talent Support Programme of Guangdong Provincial Association for Science and Technology (SKXRC202308)
/
| 〈 |
|
〉 |