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Differential regulation of the water channel protein aquaporins in chondrocytes of human knee articular cartilage by aging
Differential regulation of the water channel protein aquaporins in chondrocytes of human knee articular cartilage by aging
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Differential regulation of the water channel protein aquaporins in chondrocytes of human knee articular cartilage by aging
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Differential regulation of the water channel protein aquaporins in chondrocytes of human knee articular cartilage by aging
Differential regulation of the water channel protein aquaporins in chondrocytes of human knee articular cartilage by aging

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Differential regulation of the water channel protein aquaporins in chondrocytes of human knee articular cartilage by aging
Differential regulation of the water channel protein aquaporins in chondrocytes of human knee articular cartilage by aging
Journal Article

Differential regulation of the water channel protein aquaporins in chondrocytes of human knee articular cartilage by aging

2021
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Overview
Knee cartilage is in an aqueous environment filled with synovial fluid consisting of water, various nutrients, and ions to maintain chondrocyte homeostasis. Aquaporins (AQPs) are water channel proteins that play an important role in water exchange in cells, and AQP1, -3, and -4 are known to be expressed predominantly in cartilage. We evaluated the changes in AQP expression in chondrocytes from human knee articular cartilage in patients of different ages and identified the key factor(s) that mediate age-induced alteration in AQP expression. The mRNA and protein expression of AQP1, -3 and -4 were significantly decreased in fibrocartilage compared to hyaline cartilage and in articular cartilage from older osteoarthritis patients compared to that from young patients. Gene and protein expression of AQP1, -3 and -4 were altered during the chondrogenic differentiation of C3H10T1/2 cells. The causative factors for age-associated decrease in AQP included H 2 O 2 , TNFα, and HMGB1 for AQP1, -3, and -4, respectively. In particular, the protective effect of AQP4 reduction following HMGB1 neutralization was noteworthy. The identification of other potent molecules that regulate AQP expression represents a promising therapeutic approach to suppress cartilage degeneration during aging.