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Expression and Activity of Hyaluronidase in Human Periodontal Ligament Fibroblasts
Author(s) -
Ohno Shigeru,
Ijuin Chise,
Doi Takeyoshi,
Yoneno Kiyoshi,
Tanne Kazuo
Publication year - 2002
Publication title -
journal of periodontology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.036
H-Index - 156
eISSN - 1943-3670
pISSN - 0022-3492
DOI - 10.1902/jop.2002.73.11.1331
Subject(s) - hyaluronidase , periodontal fiber , chemistry , extracellular matrix , proinflammatory cytokine , zymography , stimulation , reverse transcription polymerase chain reaction , tumor necrosis factor alpha , real time polymerase chain reaction , messenger rna , microbiology and biotechnology , inflammation , andrology , extracellular , hyaluronic acid , matrix metalloproteinase , biology , biochemistry , enzyme , immunology , endocrinology , medicine , anatomy , gene , dentistry
Background: Hyaluronan is a major component of the extracellular matrix of periodontal ligament (PDL) contributing to the structural and functional integrity. Hyaluronans contribute to the buffering effect of the PDL during chewing, and they are also important in inflammation and wound healing. Hyaluronan is known to be synthesized and turned over by the resident PDL cells, although the mechanisms of hyaluronan metabolism still remain unclear. Hyaluronidase (HAase), an endoglycosidase, degrades hyaluronan into small fragments. Currently, 3 human HAases, HYAL1, HYAL2, and PH‐20, have been identified and well characterized. Methods: This study was conducted to investigate the expression and activity of these HAases in cultured human PDL fibroblasts and to elucidate the mechanisms involved in hyaluronan metabolism under normal and inflammatory conditions. Human PDL fibroblasts derived from the periodontium of 3 premolars were cultured with or without interleukin (IL)‐1β (0.1 to 10 ng/ml) and tumor necrosis factor (TNF)‐α (1 to 100 ng/ml) for 0 to 48 hours. The expression of HAase mRNA was assessed by reverse transcription‐polymerase chain reaction (RT‐PCR) and quantitative real‐time PCR, and the enzymatic activity was examined using hyaluronan zymography. Results: PDL fibroblasts expressed HYAL1 and HYAL2 mRNAs, but not PH‐20 mRNA. The expression of HYAL1 mRNA was enhanced by about 3.5‐ and 3.7‐fold at maximum after 1‐hour stimulation with 1 ng/ml IL‐1β and after 3‐hour stimulation with 10 ng/ml TNF‐α, respectively. The expression of HYAL2 and PH‐20 mRNAs was not affected by stimulation with cytokines. HAase activity was detected in conditioned medium from PDL fibroblast cultures, and the activity was enhanced by treatment with 10 ng/ml TNF‐α. Conclusion: These results suggest that PDL fibroblasts express HAases and generate HAase activity essential for extracellular hyaluronan metabolism under physiological and inflammatory conditions. J Periodontol 2002;73:1331‐1337.