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. 2000 Jun 19;191(12):2031–2038. doi: 10.1084/jem.191.12.2031

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© 2000 The Rockefeller University Press

This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).

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Proliferation of naive T cells from mice reconstituted with stem cells infected with Bcl-X_L virus. Naive CD4⁺ T cells isolated from the lethally irradiated mice reconstituted with bone marrow stem cells infected with control or Bcl-X_L virus (see Fig. 5) were cultured with mitomycin C–treated APCs and a range of OVA peptide in 96-well plates. Plates were pulsed with [³H]thymidine for 6 h on days 1 and 2 of activation, and the incorporated radioactivity was measured.

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