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Adaptive immunity in jawless fish

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Jawless vertebrates, which today consist entirely of lampreys and hagfish, have an adaptive immune system similar to that found in jawed vertebrates. The cells of the agnathan AIS have roles roughly equivalent to those of B-cells and T-cells, with three lymphocyte lineages identified so far:

VLRA and VLRB were identified in 2009,[1] while VLRC was discovered in 2013.[3] Instead of immunoglobulins, they use variable lymphocyte receptors.

Antigen receptors

Jawless vertebrates do not have immunoglobulins (Igs), the key proteins to B-cells and T-cells. However, they do possess a system of leucin-rich repeat (LRR) proteins that make up variable lymphocyte receptors (VLRs). This system can produce roughly the same number of potential receptors that the Ig-based system found in jawed vertebrates can.[4] Instead of recombination-activating genes (RAGs), genes coding for VLRs can be altered by a family of cytidine deaminases known as APOBEC, possibly through gene conversion.[5] Cytidine deaminase 1 is associated with the assembly of VLRA and VLRC and cytidine deaminase 2 appears to assemble VLRB.[1][3]

Evolution

The gene expression profiles of lymphocyte-like cells (LLCs) in jawless vertebrates indicate that VLRB+ LLCs and B cells share a common ancestor, and VLRA+ and VLRC+ LLCs and T cells share a common ancestor.[6] Like B cells and T cells, the development of VLRB+ LLCs is spatially separated from the development of VLRA+ and VLRC+ LLCs. VLRB+ LLCs and B cells develop in hematopoietic tissues: VLRB+ LLCs develop in the typhlosole and kidneys and B cells develop in bone marrow. VLRA+ and VLRC+ LLCs develop in a thymus-like organ called the thymoid, similar to T cells developing in the thymus.[7] VLRB molecules and B cells can directly bind to antigens and VLRB-transfected cells secrete VLRB protein products, similar to B cells in jawed vertebrates. VLRA+ LLCs were unable to bind Bacillus anthracis, Escherichia coli, Salmonella typhimurium, or Streptococcus pneumoniae before or after immunization, suggesting that VLRAs require antigen processing like TCRs.[1] However, MHCs or MHC-like molecules that could present processed antigens have not been found in lampreys,[8] and some VLRAs expressed in yeast were able to directly bind to antigens.[9] The antigen binding of VLRCs has not been studied.[10] However, the VLRC gene is close in proximity and sequence to the VLRA gene and the two are often co-expressed in LLCs, suggesting that both are TCR-like receptors.[3]

References

  1. ^ a b c d e Guo, Peng; Hirano, Masayuki; Herrin, Brantley R.; Li, Jianxu; Yu, Cuiling; Sadlonova, Andrea; Cooper, Max D. (2009-05-27). "Dual nature of the adaptive immune system in lampreys". Nature. 459 (7248): 796–801. Bibcode:2009Natur.459..796G. doi:10.1038/nature08068. ISSN 0028-0836. PMC 2714547. PMID 19474790.
  2. ^ Kishishita, Natsuko; Nagawa, Fumikiyo (March 2014). "Evolution of adaptive immunity: implications of a third lymphocyte lineage in lampreys". BioEssays. 36 (3): 244–250. doi:10.1002/bies.201300145. ISSN 1521-1878. PMID 24853392.
  3. ^ a b c Hirano, Masayuki; Guo, Peng; McCurley, Nathanael; Schorpp, Michael; Das, Sabyasachi; Boehm, Thomas; Cooper, Max D. (2013-08-11). "Evolutionary implications of a third lymphocyte lineage in lampreys". Nature. 501 (7467): 435–438. Bibcode:2013Natur.501..435H. doi:10.1038/nature12467. ISSN 0028-0836. PMC 3901013. PMID 23934109.
  4. ^ Cooper, Max D.; Alder, Matthew N. (2006-02-24). "The evolution of adaptive immune systems". Cell. 124 (4): 815–822. doi:10.1016/j.cell.2006.02.001. ISSN 0092-8674. PMID 16497590.
  5. ^ Hirano, Masayuki (August 2015). "Evolution of vertebrate adaptive immunity: immune cells and tissues, and AID/APOBEC cytidine deaminases". BioEssays. 37 (8): 877–887. doi:10.1002/bies.201400178. ISSN 1521-1878. PMID 26212221.
  6. ^ Kasamatsu, Jun (January 2013). "Evolution of innate and adaptive immune systems in jawless vertebrates". Microbiology and Immunology. 57 (1): 1–12. doi:10.1111/j.1348-0421.2012.00500.x. ISSN 0385-5600. PMID 22924515.
  7. ^ Bajoghli, Baubak; Guo, Peng; Aghaallaei, Narges; Hirano, Masayuki; Strohmeier, Christine; McCurley, Nathanael; Bockman, Dale E.; Schorpp, Michael; Cooper, Max D. (2011-02-03). "A thymus candidate in lampreys". Nature. 470 (7332): 90–94. Bibcode:2011Natur.470...90B. doi:10.1038/nature09655. ISSN 0028-0836. PMID 21293377.
  8. ^ Mayer, Werner E.; Uinuk-ool, Tatiana; Tichy, Herbert; Gartland, Lanier A.; Klein, Jan; Cooper, Max D. (2002-10-29). "Isolation and characterization of lymphocyte-like cells from a lamprey". Proceedings of the National Academy of Sciences. 99 (22): 14350–14355. Bibcode:2002PNAS...9914350M. doi:10.1073/pnas.212527499. ISSN 0027-8424. PMC 137887. PMID 12388781.
  9. ^ Deng, Lu; Velikovsky, C. Alejandro; Xu, Gang; Iyer, Lakshminarayan M.; Tasumi, Satoshi; Kerzic, Melissa C.; Flajnik, Martin F.; Aravind, L.; Pancer, Zeev (2010-07-27). "A structural basis for antigen recognition by the T cell-like lymphocytes of sea lamprey". Proceedings of the National Academy of Sciences. 107 (30): 13408–13413. Bibcode:2010PNAS..10713408D. doi:10.1073/pnas.1005475107. ISSN 0027-8424. PMC 2922149. PMID 20616002.
  10. ^ Boehm, Thomas; Hirano, Masayuki; Holland, Stephen J.; Das, Sabyasachi; Schorpp, Michael; Cooper, Max D. (2018-04-26). "Evolution of Alternative Adaptive Immune Systems in Vertebrates". Annual Review of Immunology. 36 (1): 19–42. doi:10.1146/annurev-immunol-042617-053028. hdl:21.11116/0000-0001-F62D-8. ISSN 0732-0582. PMID 29144837.

Further reading