Lymphotoxin (LT) is a member of the proinflammatory TNF family of cytokines that plays a critical role in the development of lymphoid tissue. It has previously been reported that the presence of the LTα transgene under the control of the rat insulin promoter results in inflammation at the sites of transgene expression. LTα transgene expression results in expression of the adhesion molecules VCAM, ICAM, peripheral node addressin (a marker of peripheral lymph nodes), and mucosal addressin cellular adhesion molecule (a marker of mucosal lymphoid tissue, including mesenteric lymph nodes). In this study to determine the mechanisms by which LT promotes inflammation and lymphoid tissue organization, we analyzed the regulation of expression of adhesion molecules and chemokines in LT transgenic mice. The results demonstrate that LTα3 induces expression of the adhesion molecules VCAM, ICAM, and mucosal addressin cellular adhesion molecule as well as the chemokines RANTES, IFN-inducible protein-10, and monocyte chemotactic protein-1, while LTαβ is required for the induction of peripheral node addressin that may contribute to the recruitment of L-selectin high CD44 low naive T cells. These data provide candidate mediators of LT-induced inflammation as well as potential mechanisms by which LTα and LTαβ may differentially promote the development of mesenteric and peripheral lymph nodes.