期刊
ELIFE
卷 10, 期 -, 页码 -出版社
ELIFE SCIENCES PUBLICATIONS LTD
DOI: 10.7554/eLife.64881
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- Deutsche Forschungsgemeinschaft [STR 1095/6-1, 82DZL002A, SFB/TRR57]
Expression levels of CX3CR1 on immune cells play a significant role in maintaining tissue homeostasis under physiological and pathological conditions. Recent studies suggest that misfolded proteins, such as polymers or amyloid fibrils, can regulate CX3CR1 expression, providing evidence for involvement in Z-AAT-related disorders. This highlights the importance of understanding the role of misfolded proteins in regulating CX3CR1.
Expression levels of CX3CR1 (C-X3-C motif chemokine receptor 1) on immune cells have significant importance in maintaining tissue homeostasis under physiological and pathological conditions. The factors implicated in the regulation of CX3CR1 and its specific ligand CX3CL1 (fractalkine) expression remain largely unknown. Recent studies provide evidence that host's misfolded proteins occurring in the forms of polymers or amyloid fibrils can regulate CX3CR1 expression. Herein, a novel example demonstrates that polymers of human ZZ alpha-1 antitrypsin (Z-AAT) protein, resulting from its conformational misfolding due to the Z (G1u342Lys) mutation in SERPINA1 gene, strongly lower CX3CR1 mRNA expression in human peripheral blood mononuclear cells (PBMCs). This parallels with increase of intracellular levels of CX3CR1 and Z-AAT proteins. Presented data indicate the involvement of the CX3CR1 pathway in the Z-AAT-related disorders and further support the role of misfolded proteins in CX3CR1 regulation.
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