CD49d Overexpression and T Cell Autoimmunity

• Published in: The Journal of immunology (1950) Vol. 171; no. 2; pp. 745 - 753
• Main Authors: Mo, Ru-Ran, Eisenbraun, Julie K, Sonstein, Joanne, Craig, Ronald A, Curtis, Jeffrey L, Stoolman, Lloyd M, Chen, Jun, Yung, Raymond L
• Format: Journal Article
• Language: English
• Published: United States Am Assoc Immnol 15.07.2003
• Subjects: Adoptive Transfer; Animals; Antibodies, Antinuclear - biosynthesis; Autoimmunity - genetics; Autoimmunity - immunology; Cell Adhesion - genetics; Cell Adhesion - immunology; Cell Division - genetics; Cell Division - immunology; Cell Line - immunology; Cell Line - metabolism; Cell Line - transplantation; Cell Movement - genetics; Cell Movement - immunology; Cytotoxicity, Immunologic - genetics; Endothelium, Vascular - immunology; Endothelium, Vascular - metabolism; Enzyme-Linked Immunosorbent Assay; Female; Integrin alpha4 - biosynthesis; Integrin alpha4 - genetics; Mice; Mice, Inbred AKR; Mice, Inbred MRL lpr; Phosphorylation; Spleen - cytology; Spleen - immunology; T-Lymphocytes - cytology; T-Lymphocytes - immunology; T-Lymphocytes - metabolism; Transfection - methods; Tyrosine - metabolism
• ISSN: 0022-1767; 1550-6606
• DOI: 10.4049/jimmunol.171.2.745

D10.G4.1 (D10) cells, a murine conalbumin-reactive Th2 cell line, made to overexpress the beta(2) integrin LFA-1 by pharmacological manipulation or by transfection become autoreactive and are capable of inducing in vivo autoimmunity. However, whether this is specific to LFA-1 and whether overexpression of other T cell integrin molecules has the same effect are unknown. We examined the functional consequences of T cell CD49d (alpha(4) integrin) overexpression by transfecting murine CD49d cDNA into D10 cells. Similar to the LFA-1-transfected cells, the CD49d-overexpressing T cells are autoreactive and proliferate in response to APCs in an MHC class II-dependent manner in the absence of nominal Ag. Additionally, CD49d overexpression is associated with increased in vitro adhesion to endothelial cells and increased in vivo splenic homing. However, in contrast to LFA-1 overexpression, increased T cell CD49d expression is not associated with autoreactive cytotoxicity or the ability to induce in vivo autoimmunity. In addition to the novel observation that CD49d overexpression is sufficient to induce T cell autoreactivity, our results also support the hypothesis that the ability to induce in vivo autoimmunity is related to T cell cytotoxicity and not to T cell proliferation function in the D10 murine adoptive transfer model of autoimmunity.