Women at work in Mali: the case of the Markala Cooperative

African Studies Center Working Paper No. 5

Culture and Characterization of Murine Dendritic Thy-1+ Epidermal Cells**Portions of this work were presented at the Annual Meeting of The Society for Investigative Dermatology, Inc., Washington, D.C., May 1–5, 1985.

Although numerous advances have been made in characterizing the phenotype, ontogeny, ultrastructure, and cyrochemistry of the murine Thy-1+ dendritic epidermal cell (Thy-1+ EC), elucidation of its functional qualities has been hampered by the difficulty in preparing pure populations of these cells. We therefore sought to obtain expanded, purified populations of Thy-1+ EC using culture techniques. Since Thy-1+ EC are bone marrow-derived, density gradient enriched populations of freshly harvested epidermal cells (FH-EC) were placed in culture under conditions known or suspected to promote mitogenesis among leukocyte subsets. FH-EC prepared from truncal skin of C3H/HeN mice (Thy-1.2+) were cultured at 37°C in 5% CO2 in complete medium (CM) of Eagle's Hanks' amino acid with 10% fetal calf serum, nutrients, and antibiotics at 106 FH-EC/well in 24-well culture plates. CM was supplemented with one or more of the following: concanavalin A (Con-A), interleukin-1/epidermal cell-derived thymocyte-activating factor (IL-l/ETAF), IL-2, IL-3. γ interferon, indomethacin (IM), and anti-Thy-1.2 antibody. Media with appropriate supplements were changed every 2-3 days. Freshly isolated, enriched FH-EC contained 7-20% Thy-1+ EC (defined as brightly fluorescing cells readily distinguishable from weakly fluorescing keratinocytes), which also stained with antibodies directed against asialo GM1, Ly 5.1, and vimentin but did not stain with antibodies to other T cell-, B cell- or macrophage phenotypic markers. Analysis of 10 separate cultures revealed a 3- to 10-fold expansion of nonkeratinocyte Thy-I ± cells after 21 ± 4 days in culture in CM supplemented with Con-A and IM, and 70-100% of viable cells after expansion were Thy- 1+. Phenotypic analysis of expanded cells revealed the emergence in 10 separate cultures of one two mutually exclusive distinct populations: one Thy-1+, asialo GM1+, L3T4- (natural killer phenotype) and the other Thy-1+, asialo GM1+, L3T4+ (T helper phenotype). Experiments designed to explain the emergence of an L3T4+ (T helper phenotype). Experiments designed to explain the emergence of an L3T4+ population suggest that phenotypic modulation occurred in vitro