TY - JOUR
T1 - Migration of Thy-1+ dendritic epidermal cells (Thy-1+DEC)
T2 - Ly48 and TNF-α are responsible for the migration of Thy-1+DEC to the epidermis
AU - Tamaki, Kunihiko
AU - Saitoh, Atsushi
AU - Gaspari, Anthony A.
AU - Yasaka, Nami
AU - Furue, Masutaka
PY - 1994/9
Y1 - 1994/9
N2 - Thy-1+ dendritic epidermal cells (Thy-1+DEC) are mainly T cells that express T-cell receptor γ and δ chains with limited diversity of γδ, mainly γ3δ1; such γ3δ1 TCR-bearing Thy-1+DEC originate from day 16 fetal thymic cells. To understand the migratory capability of Thy-1+DEC, we developed an in vitro model, using skin organ culture. First, emigration of Thy1+DEC from the epidermis was examined. Ear skin from C3H/He mice was separated into two parts and incubated for 3 d with dermal side down. Thy-1+DEC emigrated from the epidermis into the dermis and then migrated out of the skin into the culture medium. Next, immigration of Thy-1+DEC into the epidermis was examined. Thy-1+DEC were depleted in vivo by daily application of clobetazole propionate solution topically onto the ears of C3H/He mice. Seven days later, ear skin was harvested, separated, and cultured with the dermal side up with syngeneic epidermal cell suspensions with a migration chamber for 3 d. It was found that 1) Thy-1+DEC immigrated into the Thy-1+DEC depleted epidermis as well as into untreated epidermis, and 2) the migratory capability of Thy-1+DEC was directly proved by a biolabeling technique with PKH-26. Blocking studies with various antibodies revealed that leukosialin (S11 monoclonal antibodies) and TNFα were important for Thy-1+DEC migration. Thus, Thy-1+DEC retain the potential for migration in vitro, and leukosialin and TNFα are partially responsible for the migration of Thy-1+DEC into the epidermis.
AB - Thy-1+ dendritic epidermal cells (Thy-1+DEC) are mainly T cells that express T-cell receptor γ and δ chains with limited diversity of γδ, mainly γ3δ1; such γ3δ1 TCR-bearing Thy-1+DEC originate from day 16 fetal thymic cells. To understand the migratory capability of Thy-1+DEC, we developed an in vitro model, using skin organ culture. First, emigration of Thy1+DEC from the epidermis was examined. Ear skin from C3H/He mice was separated into two parts and incubated for 3 d with dermal side down. Thy-1+DEC emigrated from the epidermis into the dermis and then migrated out of the skin into the culture medium. Next, immigration of Thy-1+DEC into the epidermis was examined. Thy-1+DEC were depleted in vivo by daily application of clobetazole propionate solution topically onto the ears of C3H/He mice. Seven days later, ear skin was harvested, separated, and cultured with the dermal side up with syngeneic epidermal cell suspensions with a migration chamber for 3 d. It was found that 1) Thy-1+DEC immigrated into the Thy-1+DEC depleted epidermis as well as into untreated epidermis, and 2) the migratory capability of Thy-1+DEC was directly proved by a biolabeling technique with PKH-26. Blocking studies with various antibodies revealed that leukosialin (S11 monoclonal antibodies) and TNFα were important for Thy-1+DEC migration. Thus, Thy-1+DEC retain the potential for migration in vitro, and leukosialin and TNFα are partially responsible for the migration of Thy-1+DEC into the epidermis.
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U2 - 10.1111/1523-1747.ep12394437
DO - 10.1111/1523-1747.ep12394437
M3 - Article
C2 - 7521373
AN - SCOPUS:0028081565
SN - 0022-202X
VL - 103
SP - 290
EP - 294
JO - Journal of Investigative Dermatology
JF - Journal of Investigative Dermatology
IS - 3
ER -