An atlas of human siglecs integrates expression, affinity, and cis/trans sialoglycan recognition profiles

All living cells have a sugar-coat that facilitates communication. Sialic acids cap mammalian glycans and are recognized by immune cells through sialic acid-binding immunoglobulin-like lectins (Siglecs) that regulate signaling by their cytoplasmic motifs. Inconsistent reports of Siglecs expression and sialoglycan recognition limit their therapeutic potential. Here we investigate 14 functional human Siglecs for their expression, glycan interactions and affinities. SIGLEC mRNA is broad in blood-derived monocytes and dendritic cells, restricted in natural-killer/B cells and absent in T cells, with similar Siglec-proteins expression in splenocytes. Binding to 114 glycans across 274 glycan microarrays, 220 splenocytes-assays and 132 cell-based arrays, reveal Siglecs functional relationships. Siglec-sialoglycan interactions are affected by sialic acid type (N-acetylneuraminic acid and N-glycolylneuraminic acid), 9-O-acetylation, linkage, sulfation, and carrier, are of varying affinities ( ~ 10 nM to µM/mM), and cis interactions are key regulatory features. This functional atlas enhances Siglecs potential as biomarkers and immunotherapy targets, switches or immune checkpoints for cancer and other diseases.

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Publication Details

Journal
Nature Communications
Published
2026-04-25
DOI
https://doi.org/10.1038/s41467-026-71086-8
Primary Topic
Glycosylation and Glycoproteins Research
Type
article
Field-Weighted Citation Impact
0.00

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article

An atlas of human siglecs integrates expression, affinity, and cis/trans sialoglycan recognition profiles

Hai Yu, Lori J. West, Vered Padler‐Karavani, Hongzhi Cao et al.
Nature Communications
Glycosylation and Glycoproteins Research
article

An atlas of human siglecs integrates expression, affinity, and cis/trans sialoglycan recognition profiles

Hai Yu, Lori J. West, Vered Padler‐Karavani, Hongzhi Cao, Edward N. Schmidt, Kelli A. McCord, Shani Leviatan Ben‐Arye, Fahima Mozaneh, Matthew Scott Macauley, Ronit Rosenfeld, Zeinab Jame-Chenarboo, Jaesoo Jung, Xi Chen, Claire Guetta-Oz, Kan Zhong
article en

Abstract

All living cells have a sugar-coat that facilitates communication. Sialic acids cap mammalian glycans and are recognized by immune cells through sialic acid-binding immunoglobulin-like lectins (Siglecs) that regulate signaling by their cytoplasmic motifs. Inconsistent reports of Siglecs expression and sialoglycan recognition limit their therapeutic potential. Here we investigate 14 functional human Siglecs for their expression, glycan interactions and affinities. SIGLEC mRNA is broad in blood-derived monocytes and dendritic cells, restricted in natural-killer/B cells and absent in T cells, with similar Siglec-proteins expression in splenocytes. Binding to 114 glycans across 274 glycan microarrays, 220 splenocytes-assays and 132 cell-based arrays, reveal Siglecs functional relationships. Siglec-sialoglycan interactions are affected by sialic acid type (N-acetylneuraminic acid and N-glycolylneuraminic acid), 9-O-acetylation, linkage, sulfation, and carrier, are of varying affinities ( ~ 10 nM to µM/mM), and cis interactions are key regulatory features. This functional atlas enhances Siglecs potential as biomarkers and immunotherapy targets, switches or immune checkpoints for cancer and other diseases.

Nature Communications
Israel Institute for Biological Research (IL), University of Alberta (CA), Tel Aviv University (IL), Baylor College of Medicine (US), Qingdao National Laboratory for Marine Science and Technology (CN), Women and Children’s Health Research Institute (CA), Ocean University of China (CN), University of California, Davis (US)
European Commission, Canada Research Chairs, Canadian Network for Research and Innovation in Machining Technology, Natural Sciences and Engineering Research Council of Canada, Council for Higher Education, National Institutes of Health, Horizon 2020 Framework Programme, Natural Sciences and Engineering Research Council of Canada, Canadian Glycomics Network, Planning and Budgeting Committee of the Council for Higher Education of Israel, Division of Chemistry
Openalex Percentile: Top 13%
Glycosylation and Glycoproteins Research
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