Key result
Sympathetic ablation with 6-hydroxydopamine hydrobromide significantly increased beta-adrenergic receptor density on T and B spleen cells and altered Thy-1.2 and Lyt-2 surface antigen distribution.
Why the study?
Does sympathetic ablation alter lymphocyte membrane properties in mice?
Does sympathetic ablation alter lymphocyte membrane properties in mice?
Sympathetic nervous system ablation alters the distribution of beta-adrenergic receptors and surface antigens on splenic lymphocytes in mice, suggesting a role for sympathetic innervation in immune cell regulation.
Answers are grounded in this paper and cite their sources.
No clinical implications; leaves open sympathetic regulation of human lymphocyte function pending translational studies.
Ablation of the peripheral sympathetic nervous system by treatment of adult (axotomy) and neonatal (sympathectomy) mice with 6-hydroxydopamine hydrobromide produced significant changes in the distribution of cell surface molecules detected on spleen lymphocyte populations. The surface molecules that were studied consisted of the beta-adrenergic receptor and the Thy-1.2 and Lyt-2 surface antigens associated with lymphocyte subpopulations. beta-Adrenergic receptor density, as measured by 3H-dihydroalprenolol binding, was found to be significantly higher on control mouse splenic B cells than on T cells. beta-Adrenergic receptor density was seen to increase in both T and B spleen cell populations after axotomy. The Thy-1.2 and Lyt-2 surface antigens present on cell populations from mouse spleens were labeled using fluorescent monoclonal antibodies and quantitated using a fluorescence-activated cell sorter. A significant increase in the percentage of Thy-1.2 positive cells represented among the total spleen lymphocyte population was detected in axotomized mice. A corresponding increase in the representation of Lyt-2-positive cells, a subset of the Thy-1.2-positive population, was also found. In contrast, while the percentage of Thy-1.2-positive cells per total spleen lymphocyte population were not found to differ between control and sympathectomized mice, a significantly lower percentage of Lyt-2 positive cells within the Thy-1.2-positive population appeared in sympathectomized mice. Suppressor/cytotoxic cell function, as well as properties relating to the recognition of major histocompatibility complex antigens, have been associated with the Lyt-2 antigen. The relative distributions of lymphocyte subpopulations, as indicated by surface markers, and their beta-adrenergic receptors may play an important role in the physiologic functions and interactions between lymphocytes that respond to sympathetic nervous system innervation.
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Miles et al. (1985) studied this question. Sympathetic ablation (6-hydroxydopamine hydrobromide) vs. Control mice was evaluated on Distribution of cell surface molecules (beta-adrenergic receptor, Thy-1.2, and Lyt-2) on spleen lymphocytes. Sympathetic ablation with 6-hydroxydopamine hydrobromide significantly increased beta-adrenergic receptor density on T and B spleen cells and altered Thy-1.2 and Lyt-2 surface antigen distribution.
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