E-mail Print PDF

Benjamin Ortiz, Professor of Biology

Email: This e-mail address is being protected from spambots. You need JavaScript enabled to view it
Office: 800N
Phone: (212) 772-5670
Lab: 800 (212) 650-3383
Fax: (212) 772-5227

Lab Web Site: http://ortiz.bioweb.hunter.cuny.edu


Research Interest:

Gene regulation and genetic engineering of T cells

T cells are the major organizers of the adaptive immune response, and a target of viruses such as HIV and HTLV-1 that cause currently incurable diseases.  T cells can also be targeted to eliminate cancer cells in an organism by equipping them (through genetic engineering) with known antigen receptor genes.  Such known receptors now exist targeting various cancers including those of prostate, skin and blood cell origin.  T cells develop from hematopoeitic stem cells that reside in the bone marrow.  This process is governed by incompletely understood gene regulatory mechanisms that execute the T cell genetic program.  Our laboratory investigates gene regulation during T cell development.  We use both in vivo transgenic mouse models as well as newly developed technology for in vitro T cell development from embryonic stem cells.  Our focus has been on the regulation of the gene locus encoding the alpha chain of the T cell receptor (TCRa), particularly its locus control region (LCR).  Appropriately regulated expression of the TCRa gene is essential for the development of virtually all of the circulating T cells in the body. The TCRa LCR has powerful properties that provide a linked gene with a predictable pattern of gene expression, in terms of level, developmental timing and cell-type distribution.  It also bears a strong, but poorly understood, insulation capacity that provides LCR-linked transgenes with integration site-independence when inserted into the genome.  Our work to date has identified numerous sub-sequences of the TCRa LCR that support its various properties. Molecular investigations of these sequence elements (and their interactions) are expected to reveal components required for generating proper TCRa gene regulation in vivo and completion of T cell development.  Through our translational research collaborations, our work will also provide tools to establish robust, predictable and specific therapeutic gene expression in T cells via eventual gene therapy applications targeted at specific cancer cell types and T cell viral diseases.  Our lab’s reagents and technologies have enabled us to additionally contribute to collaborations with other groups investigating important aspects of T cell development and function.


Selected Publications


Last Updated ( Tuesday, 09 February 2016 18:17 )