Allorecognition, or the response of an individual to non-self antigens expressed on conspecific tissues, forms the basis for the rejection of life-saving organ transplants in humans. Despite extensive studies in mammalian models of allorecognition, safe and effective methods for preventing graft rejection are still lacking. In this grant application, we propose to extend our fundamental investigations into the mechanisms of allorecognition in an invertebrate model organism, Hydractinia symbiolongicarpus. Hydractinia is a colonial marine invertebrate that displays an unambiguous fusion/rejection response regulated by a highly specific allorecognition system. Through funding provided by an exploratory (R21) grant from the NIH, we have already identified two candidate genes, alr1 and alr2, that dictate fusion/rejection phenotypes in Hydractinia. We have also established reproducible experimental systems to track chimerism in histocompatible and incompatible fusion partners and investigate its effects on allotolerance.
The specific aims of the current proposal are to (1) functionally characterize alr genes, gene products, and interacting proteins;(2) further the genetic characterization of Hydractinia allorecognition;and (3) assess the effect of genetic distance/degree of histo-incompatibility on the stability of chimerism and allotolerance. The contribution of ?simple? model organisms to detailed understanding of biological processes in higher metazoans is underscored by discoveries made in Drosophila (host defense), C. elegans (aging), and zebra fish (organogenesis). The molecular characterization of the Hydractinia allorecognition system would establish this invertebrate organism as an invaluable model for probing fundamental processes relevant to solid organ, bone marrow, and stem cell transplantation.

Public Health Relevance

The success of transplantation in humans is hindered by rejection of the transplanted organ and by the toxicity of immunosuppressive medications. Understanding the earliest events that trigger rejection is essential for developing effective and safe therapies. Here we propose to use a simple marine organism endowed with the ability to reject unrelated individuals to uncover the most basic events that initiate the rejection process

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
High Priority, Short Term Project Award (R56)
Project #
1R56AI079103-01
Application #
7929960
Study Section
Special Emphasis Panel (ZRG1-III-B (09))
Program Officer
Rice, Jeffrey S
Project Start
2009-09-21
Project End
2011-08-31
Budget Start
2009-09-21
Budget End
2011-08-31
Support Year
1
Fiscal Year
2009
Total Cost
$417,098
Indirect Cost
Name
University of Pittsburgh
Department
Surgery
Type
Schools of Medicine
DUNS #
004514360
City
Pittsburgh
State
PA
Country
United States
Zip Code
15213
Rosengarten, Rafael D; Nicotra, Matthew L (2011) Model systems of invertebrate allorecognition. Curr Biol 21:R82-92
Powell, Anahid E; Moreno, Maria; Gloria-Soria, Andrea et al. (2011) Genetic Background and Allorecognition Phenotype in Hydractinia symbiolongicarpus. G3 (Bethesda) 1:499-504
Rosa, Sabrina F P; Powell, Anahid E; Rosengarten, Rafael D et al. (2010) Hydractinia allodeterminant alr1 resides in an immunoglobulin superfamily-like gene complex. Curr Biol 20:1122-7