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Inducible macropinocytosis of hyaluronan in B16-F10 melanoma cells
Authors:Henry J Greyner  Tomasz Wiraszka  Li-Shu Zhang  W Matthew Petroll  Mark E Mummert
Institution:1. Department of Psychiatry and Behavioral Health, University of North Texas Health Science Center, United States;2. Mental Sciences Institute, University of North Texas Health Science Center, United States;3. Department of Dermatology, University of Texas Southwestern Medical Center, United States;4. Department of Ophthalmology, University of Texas Southwestern Medical Center, United States
Abstract:Hyaluronan (HA) is a glycosaminoglycan composed of N-acetylglucosamine and glucuronic acid subunits. Endocytosis is thought to play an essential role in the catabolism of HA due to the intracellular compartmentalization of the HA degrading hyaluronidase enzymes. Previous investigations have shown that keratinocytes, chondrocytes and breast tumor cell lines endocytose HA via the cell surface glycoprotein, CD44. However, other cell types endocytose HA using a CD44-independent mechanism that remains to be defined. The purpose of this study was to investigate HA endocytosis in B16-F10 melanoma cells. We found that B16-F10 melanoma cells expressed CD44 on their surfaces. Unexpectedly, CD44 did not play a role in the endocytosis of HA. Electron microscopy studies revealed that B16-F10 melanoma cells exhibited membrane ruffling, a characteristic feature of macropinocytosis, only after incubating the cells with the HA co-polymer. Moreover, B16-F10 melanoma cells endocytosed HA via macropinocytosis as assessed by drug inhibition studies and the co-localization of fluorescently labeled HA with fluorescent tracers under confocal microscopy. Based on these results, we conclude that induced macropinocytosis may provide a previously unrecognized avenue for HA endocytosis in some cell types.
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