Overexpression Of Rhoh Permits To Bypass The Pre-Tcr Checkpoint

RhoH, an atypical small Rho-family GTPase, critically regulates thymocyte differentiation through the coordinated interaction with Lck and Zap70. Therefore, RhoH deficiency causes defective T cell development, leading to a paucity of mature T cells. Since there has been no gain-of-function study on RhoH before, we decided to take a transgenic approach to assess how the overexpression of RhoH affects the development of T cells. Although RhoH transgenic (RhoH(tg)) mice expressed three times more RhoH protein than wild-type mice, beta-selection, positive, and negative selection in the thymus from RhoH(tg) mice were unaltered. However, transgenic introduction of RhoH into Rag2 deficient mice resulted in the generation of CD4(+)CD8(+) (DP) thymocytes, indicating that overexpression of RhoH could bypass beta-selection without TCR beta gene rearrangement. This was confirmed by the in vitro development of DP cells from Rag2-/-RhoHtg DN3 cells on TSt-4/Dll-1 stroma in an Lck dependent manner. Collectively, our results indicate that an excess amount of RhoH is able to initiate pre-TCR signaling in the absence of pre-TCR complexes.