| Literature DB >> 30686034 |
Ildikó Bódi1, Krisztina H-Minkó1, Zsolt Prodán2, Nándor Nagy1, Imre Oláh1.
Abstract
The classical histological features of the thymus are the cortex and medulla, the Hassall's bodies as well as the lobules. Anti-pan-cytokeratin immunocytochemistry shows that the keratin staining pattern of the cortical and medullary epithelial cells is different. The medulla is further compartmentalized: it consists of keratin-positive network and keratin-negative areas. Histology of the keratin-negative area is identical with the connective tissue of the septae. The basal lamina is continuous at the capsule and septae, but it becomes discontinuous at the border between the keratin-positive network and keratin-negative area. This immunohistochemical finding is the first histological sign, which may explain that the medulla has no blood-thymus barrier. The supporting tissue of the keratin-negative area is identical with that of the septae. The connective tissue of thymic capsule and septae develops from the cranial neural crest cells, therefore we hypothesize that the keratin-negative area has neural crest origin. Blood vessels of the thymic medulla localize in the keratin-negative area. Every emigrating or immigrating immunologically competent cells should enter the keratin-negative area, therefore this area is the transit zone of the thymus. The hematoxylin-eosin staining of the thymus shows that the thymic cortico-medullary border does not represent cellular background. However, the border between keratin-positive network and keratin-negative area is determined by cellular identity (epithelial and mesenchymal tissues). Therefore, it can be assumed that the real histological and functional border is the border between the keratin-positive network and the keratin-negative area. Orv Hetil. 2019; 160(5): 163-171.Entities:
Keywords: Foxn1; cortico-medullary border; ganglionléc; keratin-negative area; keratin-positive network; keratinnegatív terület; keratinpozitív hálózat; kéreg-velő határ; neural crest; thymus
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Year: 2019 PMID: 30686034 DOI: 10.1556/650.2019.31224
Source DB: PubMed Journal: Orv Hetil ISSN: 0030-6002 Impact factor: 0.540