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Glycosylation plays an important role in regulating innate and adaptive immunity. With promising advances in structural and site-specific glycoproteomics, how to thoroughly extract important information from these multi-dimensional data has become another unresolved issue. The present study reports a comprehensive data mining strategy to systematically extract overall and altered glycan features from quantitative glycoproteome data. By applying the strategy to investigation of thymic involution, the study not only presents a high-resolution glycoproteome map of the mouse thymus, displaying distinct glycan structure patterns among immune-relevant cellular components, but also uncovers four major altered glycan features associated with thymic involution, including elevated LacdiNAc mainly on the MHC class I complex, increased sialoglycans that perform multiple immune functions, down-regulated bisecting glycans mostly linked to a sole GlcNAc branch, as well as possible shifts of glycan structures at the same glycosites. Regulatory network analyses further reveal the coordinated interactions of altered glycans with upstream regulators, including glycosyltransferases, glycosidases, and glycan-binding proteins, as well as downstream signaling pathways. These data offer valuable resources for future functional studies on glycosylation and the mechanistic investigation of thymic involution, supporting the strategy as a powerful tool for in-depth mining of structural and site-specific glycoproteome data from various biomedical samples.
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http://dx.doi.org/10.1002/advs.202502013 | DOI Listing |
Tierarztl Prax Ausg G Grosstiere Nutztiere
August 2025
Tierklinik für Reproduktionsmedizin und Neugeborenenkunde, Justus-Liebig-Universität Gießen.
In contrast to human medicine, thymic disorders receive little attention as differential diagnoses in veterinary medicine. The aim of this overview is to provide information on the current state of knowledge concerning the topographical anatomy, physiological development, and involution, function, and diseases of the thymus as well as the diagnosis of thymic disorders in various domestic mammals. Therefore, literature on this topic was searched and summarized.
View Article and Find Full Text PDFCancer Sci
September 2025
Division of Thoracic Surgery, Department of Surgery, Kyoto Prefectural University of Medicine, Graduate School of Medical Science, Kyoto, Japan.
Ectopic germinal centers (GCs) are often formed in the thymus of patients with anti-acetylcholine receptor antibody (anti-AChR Ab)-positive thymic epithelial tumors (TETs) and are considered sites where B cells undergo affinity maturation to produce high-affinity anti-AChR Abs, contributing to the development of myasthenia gravis. To evaluate the clinical relevance of these ectopic GCs, we analyzed their distribution and associations with thymic involution and anti-AChR Ab titers using paraffin-embedded surgical specimens from 79 TET patients. Thymic involution was scored, and immunohistochemistry was performed to identify cells involved in GC formation.
View Article and Find Full Text PDFInt Immunopharmacol
August 2025
Bose Institute, P-1/12 CIT Scheme VII M, Kolkata 700 054, India. Electronic address:
Cureus
July 2025
Pediatrics, Mohammed V Military Hospital, Rabat, MAR.
Mediastinal masses in children often raise concern for malignant conditions, particularly lymphoma. The thymus, which is normally prominent in infants and young children, begins its physiological involution around the age of six to seven years; however, this process is gradual and can extend into adolescence. Thymic hyperplasia beyond this age is uncommon, and it can mimic a mediastinal tumor on imaging.
View Article and Find Full Text PDFRadiat Res
August 2025
Departments of Medicine.
Survivors of the hematopoietic acute radiation syndrome (H-ARS) face delayed effects of acute radiation exposure (DEARE), including chronic immune suppression and thymic involution, for which no effective countermeasures exist. We previously demonstrated that 16,16-dimethyl prostaglandin E2 (dmPGE2) enhances H-ARS survival when administered prior to irradiation. Here, we investigated its long-term radiation protective effects on immune reconstitution at 6 and 12 months after exposure in a lethal total-body irradiation (TBI) mouse model.
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