Background: Human histo-blood group antigens (HBGA) are genetically determined glycoproteins supposed to participate in cell differentiation, adhesion, cancer metastasis and angiogenesis. In tissues, HBGA are mostly expressed in epithelial cells (EC). The EC comprising the thymocyte microenvironment play an important role in the ontogeny of the thymus. The aim of the present work is to investigate ABH HBGA in senile thymus and to characterize their expression pattern related to the process of aging.
Methods: Routine histology and immunohistochemical techniques were applied on thymus glands from senile and young individuals.
Results: Involuted thymus exhibited large areas of adipose tissue containing scattered EC, all positive for HBGA. Stromal EC revealed different morphology and intrathymic localization but uniform cytoplasmic staining for ABH antigens. Endothelial cells of blood vessels and red blood cells were intensely stained for HBGA. Only single scattered lymphocytes possessed HBGA. In contrast with senile thymus, most lymphocyte populations in the gland of young individuals, as well as the Hassall's corpuscules, expressed HBGA.
Conclusions: The epithelial framework reorganization during age-related thymus involution involves modulation in ABH antigen expression in EC. These molecules are required by thymic EC to maintain the reduced but important crosstalk with lymphocytes during involution. The diminished reactivity for ABH antigens in the lymphocytes of aged thymus might reflect the impaired communication between these two cell types. We present novel evidence for permanent presence and modulation of ABH antigen reactivity in senile thymus, supporting the view that these molecules might be developmentally regulated.
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http://dx.doi.org/10.1016/j.arcmed.2006.03.002 | DOI Listing |
Bioeng Transl Med
September 2023
Department of Biotherapy, Cancer Center and State Key Laboratory of Biotherapy West China Hospital, Sichuan University Chengdu China.
Int J Mol Sci
March 2023
Institute for Regeneration and Repair, Centre for Regenerative Medicine, University of Edinburgh, Edinburgh EH16 4UU, UK.
Aging of the immune system involves functional changes in individual cell populations, in hematopoietic tissues and at the systemic level. They are mediated by factors produced by circulating cells, niche cells, and at the systemic level. Age-related alterations in the microenvironment of the bone marrow and thymus cause a decrease in the production of naive immune cells and functional immunodeficiencies.
View Article and Find Full Text PDFRejuvenation Res
October 2022
The Stem Cells and Immune Cells Biomedical Techniques Integrated Engineering Laboratory of State and Regions, Cell Therapy Technology Transfer Medical Key Laboratory of Yunnan Province, Basic Medical Laboratory, 920th Hospital of the PLA Joint Logistics Support Force, Kunming, China.
Aging (Albany NY)
September 2020
Kunming Key Laboratory of Stem Cell and Regenerative Medicine, 920th Hospital of The PLA Joint Logistics Support Force, Kunming, Yunnan Province, China.
Exp Ther Med
June 2018
Department of Pharmacology, College of Pharmacy, Beihua University, Jilin City, Jilin 132013, P.R. China.
As a strategy to prevent the well-known immunosuppressant effects of cyclophosphamide (Cyp), the immunomodulatory effects of the polysaccharide extract of the fruit of (Turcz.) Baill. were investigated in the present study.
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