The vertebrate MHC-based allorecognition system has revealed much about T-cell function, and is beginning to yield information about NK cell function. Our understanding of the evolution of T-cells and MHC genes stops at sharks. In order to understand what other self/nonself recognition systems might operate in transplantation and cancer immunity and also to track the evolutionary origins of vertebrate MHC, we have investigated a model organism - the protochordate Botryllus schlosseri. Botryllus undergoes a natural transplant fusion (of blood vessels between distinct individuals) or rejection. Like MHC-based rejection in vertebrates, rejection in Botryllus is determined by a single, highly polymorphic histocompatibility locus we have named Fu/HC. A principle function of the Fu/HC appears to be the limitation of chimera formation in the wild to siblings. We have shown that Botryllus chimeras share somatic totipotent as well as germline progenitors resulting in germ cell and somatic cell parasitism; a comparable vertebrate condition is fetuses sharing a common blood circulation, such as in freemartin cattle. The two objective of this project are to: 1) to clone the polymorphic Fu/HC genes; and 2) to clone vertebrate MHC homologues in the Botrylluss genome. We shall test the relation of 1) to 2), and hope eventually to understand how Fu/HC self/nonself recognition works, and whether it has homologues in vertebrates.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
1R01AI041588-01A1
Application #
2638150
Study Section
Immunobiology Study Section (IMB)
Project Start
1998-03-01
Project End
2003-02-28
Budget Start
1998-03-01
Budget End
1999-02-28
Support Year
1
Fiscal Year
1998
Total Cost
Indirect Cost
Name
Stanford University
Department
Pathology
Type
Schools of Medicine
DUNS #
800771545
City
Stanford
State
CA
Country
United States
Zip Code
94305
Langenbacher, Adam D; De Tomaso, Anthony W (2016) Temporally and spatially dynamic germ cell niches in Botryllus schlosseri revealed by expression of a TGF-beta family ligand and vasa. Evodevo 7:9
Taketa, Daryl A; Nydam, Marie L; Langenbacher, Adam D et al. (2015) Molecular evolution and in vitro characterization of Botryllus histocompatibility factor. Immunogenetics 67:605-23
Munday, Roma; Rodriguez, Delany; Di Maio, Alessandro et al. (2015) Aging in the colonial chordate, Botryllus schlosseri. Invertebr Reprod Dev 59:45-50
Langenbacher, Adam D; Rodriguez, Delany; Di Maio, Alessandro et al. (2015) Whole-mount fluorescent in situ hybridization staining of the colonial tunicate Botryllus schlosseri. Genesis 53:194-201
Braden, Brian P; Taketa, Daryl A; Pierce, James D et al. (2014) Vascular regeneration in a basal chordate is due to the presence of immobile, bi-functional cells. PLoS One 9:e95460
Nydam, Marie L; Taylor, Alyssa A; De Tomaso, Anthony W (2013) Evidence for selection on a chordate histocompatibility locus. Evolution 67:487-500
Nydam, Marie L; Netuschil, Nikolai; Sanders, Erin et al. (2013) The candidate histocompatibility locus of a Basal chordate encodes two highly polymorphic proteins. PLoS One 8:e65980
Nydam, Marie L; Hoang, Tinya A; Shanley, Katie M et al. (2013) Molecular evolution of a polymorphic HSP40-like protein encoded in the histocompatibility locus of an invertebrate chordate. Dev Comp Immunol 41:128-36
McKitrick, Tanya R; Muscat, Christina C; Pierce, James D et al. (2011) Allorecognition in a basal chordate consists of independent activating and inhibitory pathways. Immunity 34:616-26
Carpenter, Meredith A; Powell, John H; Ishizuka, Katherine J et al. (2011) Growth and long-term somatic and germline chimerism following fusion of juvenile Botryllus schlosseri. Biol Bull 220:57-70

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