TY - JOUR
T1 - Thy-1+ dendritic epidermal cells belong to the T-cell lineage
AU - Stingl, G.
AU - Gunter, K. C.
AU - Tschachler, E.
AU - Yamada, H.
AU - Lechler, R. I.
AU - Yokoyama, W. M.
AU - Steiner, G.
AU - Germain, R. N.
AU - Shevach, E. M.
PY - 1987
Y1 - 1987
N2 - The murine epidermis contains a population of dendritic, Thy-1+ cells (Thy-1+ DEC). Although it is now clear that these cells are of bone marrow origin, extensive morphological, histochemical, and cell-membrane marker studies have not definitively placed them in any known hematopoietic differentiation pathway. Based on the observation that Thy-1+ DEC can be propagated in vitro with Con A and interleukin 2, we have established three cell lines (Tehy 184, Tehy 245, and Yety 245) that can be continuously grown in medium with lectin-lymphokine-rich culture supernatants of rat spleen cells. With the exception of the loss of reactivity with anti-asialo-G(M1) antibodies (Tehy 184 and Tehy 245) and the gain of interleukin 2 receptor expression, the cultured cell lines bear the same surface characteristics as freshly isolated Thy-1+ DEC: Thy-1+, Ly-5+, Lyt-1-, Lyt-2-, L3T4-m Ia-, sIg-. Using Southern and RNA gel blot analysis, we now demonstrate that these Thy-1+ DEC-derived cell lines exhibit various patterns of rearrangements in the gene complexes encoding the T-cell receptor (related) β and γ chains and contain mature and/or incomplete transcripts from the T-cell receptor α- and β-chain genes, as well as transcripts from the receptor-related γ-chain genes. Tehy 184 cells, the only cells containing both mature α- and β-chain transcripts, react positively with the F23.1 monoclonal antibody, which recognizes the product of a subset of T-cell recepor β-chain variable region gene segments. This antibody precipitates a surface protein of 84-88 kDa from these cells that after reduction separates into two 40- to 44-kDa chains, characteristic of Ti α/β heterodimers. These data strongly suggest that Thy-1+ DEC belong to the T-cell lineage and point to the epidermis as a site either of immature thymocyte migration or of extrathymic T-cell differentiation.
AB - The murine epidermis contains a population of dendritic, Thy-1+ cells (Thy-1+ DEC). Although it is now clear that these cells are of bone marrow origin, extensive morphological, histochemical, and cell-membrane marker studies have not definitively placed them in any known hematopoietic differentiation pathway. Based on the observation that Thy-1+ DEC can be propagated in vitro with Con A and interleukin 2, we have established three cell lines (Tehy 184, Tehy 245, and Yety 245) that can be continuously grown in medium with lectin-lymphokine-rich culture supernatants of rat spleen cells. With the exception of the loss of reactivity with anti-asialo-G(M1) antibodies (Tehy 184 and Tehy 245) and the gain of interleukin 2 receptor expression, the cultured cell lines bear the same surface characteristics as freshly isolated Thy-1+ DEC: Thy-1+, Ly-5+, Lyt-1-, Lyt-2-, L3T4-m Ia-, sIg-. Using Southern and RNA gel blot analysis, we now demonstrate that these Thy-1+ DEC-derived cell lines exhibit various patterns of rearrangements in the gene complexes encoding the T-cell receptor (related) β and γ chains and contain mature and/or incomplete transcripts from the T-cell receptor α- and β-chain genes, as well as transcripts from the receptor-related γ-chain genes. Tehy 184 cells, the only cells containing both mature α- and β-chain transcripts, react positively with the F23.1 monoclonal antibody, which recognizes the product of a subset of T-cell recepor β-chain variable region gene segments. This antibody precipitates a surface protein of 84-88 kDa from these cells that after reduction separates into two 40- to 44-kDa chains, characteristic of Ti α/β heterodimers. These data strongly suggest that Thy-1+ DEC belong to the T-cell lineage and point to the epidermis as a site either of immature thymocyte migration or of extrathymic T-cell differentiation.
UR - http://www.scopus.com/inward/record.url?scp=0023268923&partnerID=8YFLogxK
U2 - 10.1073/pnas.84.8.2430
DO - 10.1073/pnas.84.8.2430
M3 - Article
C2 - 2882517
AN - SCOPUS:0023268923
SN - 0027-8424
VL - 84
SP - 2430
EP - 2434
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 8
ER -