URPhyM, Physiological Chemistry laboratory, NARILIS, University of Namur, Namur, Belgium.
URVI, Integrated Veterinary Research Unit, NARILIS, University of Namur, Namur, Belgium.
Sci Rep. 2022 Jun 16;12(1):10142. doi: 10.1038/s41598-022-14473-7.
Mucopolysaccharidosis IX is a lysosomal storage disorder caused by a deficiency in HYAL1, an enzyme that degrades hyaluronic acid at acidic pH. This disease causes juvenile arthritis in humans and osteoarthritis in the Hyal1 knockout mouse model. Our past research revealed that HYAL1 is strikingly upregulated (~ 25x) upon differentiation of bone marrow monocytes into osteoclasts. To investigate whether HYAL1 is involved in the differentiation and/or resorption activity of osteoclasts, and in bone remodeling in general, we analyzed several bone parameters in Hyal1 -/- mice and studied the differentiation and activity of their osteoclasts and osteoblasts when differentiated in vitro. These experiments revealed that, upon aging, HYAL1 deficient mice exhibit reduced femur length and a ~ 15% decrease in bone mineral density compared to wild-type mice. We found elevated osteoclast numbers in the femurs of these mice as well as an increase of the bone resorbing activity of Hyal1 -/- osteoclasts. Moreover, we detected decreased mineralization by Hyal1 -/- osteoblasts. Taken together with the observed accumulation of hyaluronic acid in Hyal1 -/- bones, these results support the premise that the catabolism of hyaluronic acid by osteoclasts and osteoblasts is an intrinsic part of bone remodeling.
黏多糖贮积症 IX 是一种溶酶体贮积症,由 HYAL1 缺乏引起,该酶在酸性 pH 下降解透明质酸。这种疾病在人类中引起幼年型关节炎,在 Hyal1 敲除小鼠模型中引起骨关节炎。我们过去的研究表明,HYAL1 在骨髓单核细胞分化为破骨细胞时显著上调(~25 倍)。为了研究 HYAL1 是否参与破骨细胞的分化和/或吸收活性以及骨重塑的一般过程,我们分析了 Hyal1 -/- 小鼠的几种骨参数,并研究了其破骨细胞在体外分化时的分化和活性。这些实验表明,随着年龄的增长,与野生型小鼠相比,Hyal1 缺陷型小鼠的股骨长度缩短,骨密度降低约 15%。我们发现这些小鼠的股骨中破骨细胞数量增加,Hyal1 -/- 破骨细胞的骨吸收活性增加。此外,我们检测到 Hyal1 -/- 成骨细胞的矿化减少。结合观察到的 Hyal1 -/- 骨骼中透明质酸的积累,这些结果支持这样的前提,即破骨细胞和成骨细胞对透明质酸的分解代谢是骨重塑的内在部分。