1. Terminally Differentiated Epithelial Cells of the Thymic Medulla and Skin Express Nicotinic Acetylcholine Receptor Subunit α3
- Author
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Amir Rafiq, A. Panneck, Aichurek Soultanova, and Wolfgang Kummer
- Subjects
medicine.medical_specialty ,Article Subject ,Cellular differentiation ,T cell ,Stratum granulosum ,lcsh:Medicine ,Mice, Transgenic ,Thymus Gland ,Biology ,Receptors, Nicotinic ,General Biochemistry, Genetics and Molecular Biology ,Mice ,Internal medicine ,medicine ,Animals ,Receptor ,Skin ,General Immunology and Microbiology ,Epidermis (botany) ,integumentary system ,lcsh:R ,Cell Differentiation ,Epithelial Cells ,General Medicine ,Cell biology ,Nicotinic acetylcholine receptor ,medicine.anatomical_structure ,Nicotinic agonist ,Endocrinology ,Gene Expression Regulation ,Cholinergic ,Research Article - Abstract
In the thymus, T cell maturation is influenced by cholinergic signaling, and the predominantly expressed receptor is theα3-subunit of nicotinic acetylcholine receptors, encoded by thechrna3gene. We here determined its cellular distribution utilizing an appropriate eGFP-expressing reporter mouse strain. Neither T cells (CD4, CD8) nor mesenchymal cells (desmin-positive) expressed eGFP. In the thymic medulla, eGFP-positive cells either were scattered or, more frequently, formed small clusters resembling Hassall’s corpuscles. Immunolabeling revealed that these cells were indeed terminally differentiated epithelial cells expressing keratin 10 (K10) but neither typical cortical (K8, K18) nor medullary keratins (K5, K14). These labeling patterns reflected those in the epidermis of the skin, where overlap of K10 and eGFP expression was seen in the stratum granulosum, whereas underlying basal cells displayed K5-immunoreactivity. A substantial portion of thymic eGFP-positive cells was also immunoreactive to chromogranin A, a peptide previously reported in epidermal keratinocytes in the stratum granulosum. Its fragment catestatin has multiple biological activities, including suppression of proinflammatory cytokine release from macrophages and inhibition ofα3β4 nAChR. The present findings suggest that its thymic production and/or release are under cholinergic control involving nAChR containing theα3-subunit.
- Published
- 2014
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