期刊
JOURNAL OF BIOLOGICAL CHEMISTRY
卷 290, 期 26, 页码 16077-16087出版社
AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/jbc.M115.644302
关键词
apolipoprotein D (apoD); basigin; internalization; cyclophilin A; human neuroblastoma
资金
- Canadian Institutes of Health Research [MOP-15677]
Background: ApoD appears to be a protein with multiple functions that could influence inflammatory and oxidative pathways to prevent neurotoxicity. Results: The internalization of apoD is mediated by a specific cell surface receptor. Conclusion: Basigin, a transmembrane glycoprotein, is implicated in the internalization process of apoD. Significance: This is the first evidence that a specific receptor is involved in apoD internalization. Apolipoprotein D (apoD), a member of the lipocalin family, is a 29-kDa secreted glycoprotein that binds and transports small lipophilic molecules. Expressed in several tissues, apoD is up-regulated under different stress stimuli and in a variety of pathologies. Numerous studies have revealed that overexpression of apoD led to neuroprotection in various mouse models of acute stress and neurodegeneration. This multifunctional protein is internalized in several cells types, but the specific internalization mechanism remains unknown. In this study, we demonstrate that the internalization of apoD involves a specific cell surface receptor in 293T cells, identified as the transmembrane glycoprotein basigin (BSG, CD147); more particularly, its low glycosylated form. Our results show that internalized apoD colocalizes with BSG into vesicular compartments. Down-regulation of BSG disrupted the internalization of apoD in cells. In contrast, overexpression of basigin in SH-5YSY cells, which poorly express BSG, restored the uptake of apoD. Cyclophilin A, a known ligand of BSG, competitively reduced apoD internalization, confirming that BSG is a key player in the apoD internalization process. In summary, our results demonstrate that basigin is very likely the apoD receptor and provide additional clues on the mechanisms involved in apoD-mediated functions, including neuroprotection.
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