Abstract
The multisubunit enzyme V-ATPase harbours isoforms of individual subunits. a3 is one of four 116 kDa subunit a isoforms, and it is crucial for bone resorption. We used small interfering RNA (siRNA) molecules to knock down a3 in rat osteoclast cultures. Labeled siRNA-molecules entered osteoclasts via endocytosis and knocked down the a3 mRNA. Bone resorption was decreased in siRNA-treated samples due to decreased acidification and osteoclast inactivation. Expression of a1 did not respond to decreased a3 levels, suggesting that a1 does not compensate for a3 in osteoclast cultures. Subunit a3 is thus an interesting target for novel nucleic acid therapy.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Cells, Cultured
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Endocytosis / physiology
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Isoenzymes / antagonists & inhibitors*
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Isoenzymes / genetics
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Isoenzymes / metabolism
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Osteoclasts / enzymology*
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Protein Subunits / antagonists & inhibitors
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Protein Subunits / genetics
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Protein Subunits / metabolism
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RNA, Small Interfering / genetics
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RNA, Small Interfering / metabolism*
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Rats
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Vacuolar Proton-Translocating ATPases / antagonists & inhibitors*
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Vacuolar Proton-Translocating ATPases / genetics*
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Vacuolar Proton-Translocating ATPases / metabolism
Substances
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Isoenzymes
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Protein Subunits
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RNA, Small Interfering
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Vacuolar Proton-Translocating ATPases