Monosialoganglioside GM3 is the simplest ganglioside involved in various cellular signaling. Cell surface distribution of GM3 is thought to be crucial for the function of GM3, but little is known about the cell surface GM3 distribution. It was shown that anti-GM3 monoclonal antibody binds to GM3 in sparse but not in confluent melanoma cells. Our model membrane study evidenced that monoclonal anti-GM3 antibodies showed stronger binding when GM3 was in less fluid membrane environment. Studies using fluorescent GM3 analogs suggested that GM3 was clustered in less fluid membrane. Moreover, fluorescent lifetime measurement showed that cell surface of high density melanoma cells is more fluid than that of low density cells. Lipidomics and fatty acid supplementation experiment suggested that monounsaturated fatty acid-containing phosphatidylcholine contributed to the cell density-dependent membrane fluidity. Our results indicate that anti-GM3 antibody senses GM3 clustering and the number and/or size of GM3 cluster differ between sparse and confluent melanoma cells.

Cell density-dependent membrane distribution of ganglioside GM3 in melanoma cells / M. Murate, N. Yokoyama, N. Tomishige, L. Richert, N. Humbert, B. Pollet, A. Makino, N. Kono, L. Mauri, J. Aoki, Y. Sako, S. Sonnino, N. Komura, H. Ando, M.K. Kaneko, Y. Kato, K. Inamori, J. Inokuchi, Y. Mély, K. Iwabuchi, T. Kobayashi. - In: CELLULAR AND MOLECULAR LIFE SCIENCES. - ISSN 1420-682X. - 80:6(2023 May 30), pp. 167.1-167.15. [10.1007/s00018-023-04813-9]

Cell density-dependent membrane distribution of ganglioside GM3 in melanoma cells

L. Mauri;S. Sonnino;
2023

Abstract

Monosialoganglioside GM3 is the simplest ganglioside involved in various cellular signaling. Cell surface distribution of GM3 is thought to be crucial for the function of GM3, but little is known about the cell surface GM3 distribution. It was shown that anti-GM3 monoclonal antibody binds to GM3 in sparse but not in confluent melanoma cells. Our model membrane study evidenced that monoclonal anti-GM3 antibodies showed stronger binding when GM3 was in less fluid membrane environment. Studies using fluorescent GM3 analogs suggested that GM3 was clustered in less fluid membrane. Moreover, fluorescent lifetime measurement showed that cell surface of high density melanoma cells is more fluid than that of low density cells. Lipidomics and fatty acid supplementation experiment suggested that monounsaturated fatty acid-containing phosphatidylcholine contributed to the cell density-dependent membrane fluidity. Our results indicate that anti-GM3 antibody senses GM3 clustering and the number and/or size of GM3 cluster differ between sparse and confluent melanoma cells.
Anti-ganglioside antibodies; Crypticity; Fluorescence lifetime imaging; Lipidomics; Plasma membrane
Settore BIO/10 - Biochimica
Settore BIOS-07/A - Biochimica
30-mag-2023
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/1057049
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