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Comparison of Siglec-1 Protein Networks and Expression Patterns in Sperm and Male Reproductive Tracts of Mice, Rats, and Humans

Overview
Journal Vet World
Date 2024 Apr 29
PMID 38680147
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Abstract

Background: Sialic acid-binding immunoglobulin-like lectin 1 (Siglec-1) is a transmembrane glycoprotein involved in the sialic acid (Sia)-dependent regulation of the immune system. Siglec-1 expression has recently been identified in the male reproductive tract (MRT) of several species, including humans, cattle, horses, and sheep, and may play a role in modulating fertility in a Sia-dependent manner.

Materials And Methods: In this study, protein-protein interaction (PPI) analysis of Siglec-1 was conducted to identify associated network protein conservation, and the expression of Siglec-1 in the MRT of mice and rats, including their accessory sex glands and spermatozoa was determined by immunostaining.

Results: Network analysis of proteins with Siglec-1 in mice and rats demonstrated significant similarity to human Siglec-1 networks, suggesting a similar conservation of network proteins between these species and, hence, a potential conservation role in immune modulation and function. Specific immunostaining patterns of mouse and rat testes, epididymis, ductus deferens, accessory sex gland tissues, and sperm were detected using human Siglec-1. These results confirmed that the human Siglec-1 antibody could cross-react with mouse and rat Siglec-1, suggesting that the specific expression patterns of Siglec-1 in the MRT and sperm of both mice and rats are similar to those observed in other species.

Conclusions: The conservation of Siglec-1 expression patterns in sperm and within the MRT and the similarity of protein networks for Siglec-1 across species suggest that Siglec-1 may function in a similar manner across species. These results also suggest that rodents may serve as a valuable model system for exploring the function of Siglecs in the reproductive system across species and their potential role in modulating fertility in a Sia-dependent manner.

References
1.
Roszer T . Understanding the Mysterious M2 Macrophage through Activation Markers and Effector Mechanisms. Mediators Inflamm. 2015; 2015:816460. PMC: 4452191. DOI: 10.1155/2015/816460. View

2.
Fliniaux I, Marchand G, Molinaro C, Decloquement M, Martoriati A, Marin M . Diversity of sialic acids and sialoglycoproteins in gametes and at fertilization. Front Cell Dev Biol. 2022; 10:982931. PMC: 9630641. DOI: 10.3389/fcell.2022.982931. View

3.
Pillai S, Netravali I, Cariappa A, Mattoo H . Siglecs and immune regulation. Annu Rev Immunol. 2012; 30:357-92. PMC: 3781015. DOI: 10.1146/annurev-immunol-020711-075018. View

4.
Klaus C, Liao H, Allendorf D, Brown G, Neumann H . Sialylation acts as a checkpoint for innate immune responses in the central nervous system. Glia. 2020; 69(7):1619-1636. DOI: 10.1002/glia.23945. View

5.
Barenwaldt A, Laubli H . The sialoglycan-Siglec glyco-immune checkpoint - a target for improving innate and adaptive anti-cancer immunity. Expert Opin Ther Targets. 2019; 23(10):839-853. DOI: 10.1080/14728222.2019.1667977. View