Cultivation and Phenotypic Characterization of Rabbit Epithelial Cells ExpandedEx Vivofrom Fresh and Cryopreserved Limbal and Oral Mucosal Explants

2014 ◽  
Vol 40 (3) ◽  
pp. 274-281 ◽  
Author(s):  
Daranee Promprasit ◽  
Kanokkan Bumroongkit ◽  
Chainarong Tocharus ◽  
Umnat Mevatee ◽  
Napaporn Tananuvat
1992 ◽  
Vol 2 (1) ◽  
pp. 51-66 ◽  
Author(s):  
Richard L. Boyd ◽  
Trevor J. Wilson ◽  
Andrew G. Bean ◽  
Harry A. Ward ◽  
M. Eric Gershwin

Phenotypic profiles of the thymic stromal components provide an excellent approach to elucidating the nature of the microenvironment of this organ. To address this issue in chickens, we have produced an extensive panel of 18 mAb to the thymic stroma. These mAb have been extensively characterized with respect to their phenotypic specificities and reveal that the stromal cells are equally as complex as the T cells whose maturation they direct. They further demonstrate that, in comparison to the mammalian thymus, there is a remarkable degree of conservation in thymic architecture between phylogenetically diverse species. Eleven mAb reacted with thymic epithelial cells: MUI-73 was panepithelium, MUI-54 stained all cortical and medullary epithelium but only a minority of the subcapsule, MUI-52 was specific for isolated stellate cortical epithelial cells, MUI-62, -69, and -71 were specific for the medulla (including Hassall’s corpusclelike structures), MUI-51, -53, -70, and -75 reacted only with the type-I epithelium, or discrete regions therein, lining the subcapsular and perivascular regions and MUI-58 demonstrated the antigenic similarity between the subcapsule and the medulla. Seven other mAb identified distinct isolated stromal cells throughout the cortex and medulla. Large thymocyte-rich regions, which often spanned from the outer cortex to medulla, lacked epithelial cells. These mAb should prove invaluable for determining the functional significance of thymic stromal-cell subsets to thymopoiesis.


1994 ◽  
Vol 81 (2) ◽  
pp. 117-127 ◽  
Author(s):  
Jason Yang ◽  
Raphael C. Guzman ◽  
Nikolay Popnikolov ◽  
Gautam K. Bandyopadhyay ◽  
Konstantin Christov ◽  
...  

2021 ◽  
Vol 12 ◽  
Author(s):  
Veronika Haunerdinger ◽  
Maria Domenica Moccia ◽  
Lennart Opitz ◽  
Stefano Vavassori ◽  
Hitendu Dave ◽  
...  

Thymic epithelial cells (TECs) are essential in supporting the development of mature T cells from hematopoietic progenitor cells and facilitate their lineage-commitment, proliferation, T-cell receptor repertoire selection and maturation. While animal model systems have greatly aided in elucidating the contribution of stromal cells to these intricate processes, human tissue has been more difficult to study, partly due to a lack of suitable surface markers comprehensively defining human TECs. Here, we conducted a flow cytometry based surface marker screen to reliably identify and quantify human TECs and delineate medullary from cortical subsets. These findings were validated by transcriptomic and histologic means. The combination of EpCAM, podoplanin (pdpn), CD49f and CD200 comprehensively identified human TECs and not only allowed their reliable distinction in medullary and cortical subsets but also their detailed quantitation. Transcriptomic profiling of each subset in comparison to fibroblasts and endothelial cells confirmed the identity of the different stromal cell subsets sorted according to the proposed strategy. Our dataset not only demonstrated transcriptional similarities between TEC and cells of mesenchymal origin but furthermore revealed a subset-specific distribution of a specific set of extracellular matrix-related genes in TECs. This indicates that TECs significantly contribute to the distinct compartmentalization – and thus function – of the human thymus. We applied the strategy to quantify TEC subsets in 31 immunologically healthy children, which revealed sex-specific differences of TEC composition early in life. As the distribution of mature CD4- or CD8-single-positive thymocytes was correspondingly altered, the composition of the thymic epithelial compartment may directly impact on the CD4-CD8-lineage choice of thymocytes. We prove that the plain, reliable strategy proposed here to comprehensively identify human TEC subpopulations by flow cytometry based on surface marker expression is suitable to determine their frequency and phenotype in health and disease and allows sorting of live cells for downstream analysis. Its use reaches from a reliable diagnostic tool for thymic biopsies to improved phenotypic characterization of thymic grafts intended for therapeutic use.


2004 ◽  
Vol 79 (1) ◽  
pp. 41-49 ◽  
Author(s):  
Hyun-Seung Kim ◽  
Xiu Jun Song ◽  
Cintia S de Paiva ◽  
Zhuo Chen ◽  
Stephen C Pflugfelder ◽  
...  

2014 ◽  
Vol 34 (4) ◽  
pp. 997-1003 ◽  
Author(s):  
YUNHE GAO ◽  
MEIYING LI ◽  
XUEYAN ZHANG ◽  
TINGTING BAI ◽  
GUANFAN CHI ◽  
...  

2009 ◽  
Vol 47 (01) ◽  
Author(s):  
K Hochrath ◽  
S Hillebrandt ◽  
F Lammert ◽  
B Rathkolb ◽  
H Fuchs ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document