Identification and Characterisation of the CD40-Ligand of Sigmodon hispidus

Cotton rats are an important animal model to study infectious diseases. They have demonstrated higher susceptibility to a wider variety of human pathogens than other rodents and are also the animal model of choice for pre-clinical evaluations of some vaccine candidates. However, the genome of cotton...

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Published inbioRxiv
Main Authors Li, Xuguang, Russell, Marsha, Larocque, Louise, Cao, Jingxin, Deschambault, Yvon, Varga, Jessie, Sathya N Thulasi Raman, Muralidharan, Abenaya
Format Paper
LanguageEnglish
Published Cold Spring Harbor Cold Spring Harbor Laboratory Press 01.06.2018
Subjects
Animal models
Bone marrow
CD40 antigen
CD40L protein
CD80 antigen
CD86 antigen
Cell surface
Cloning
Dendritic cells
Genomes
Immunopathogenesis
Infectious diseases
Interleukin 6
Leukocytes (granulocytic)
Ligands
Lymphocytes B
Lymphocytes T
Macrophages
Nucleotides
Open reading frames
Pathogens
Proteins
Rodents
Vaccines
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Summary:Cotton rats are an important animal model to study infectious diseases. They have demonstrated higher susceptibility to a wider variety of human pathogens than other rodents and are also the animal model of choice for pre-clinical evaluations of some vaccine candidates. However, the genome of cotton rats remains to be fully sequenced, with much fewer genes cloned and characterised compared to other rodent species. Here we report the cloning and characterization of CD40 ligand, whose human and murine counterparts are known to be expressed on a range of cell types including activated T cells and B cells, dendritic cells, granulocytes, macrophages and platelets and exerts a broad array of immune responses. The cDNA for cotton rat CD40L we isolated is comprised of 1104 nucleotides with an open reading frame (ORF) of 783bp coding for a 260 amino acid protein. The recombinant cotton rat CD40L protein was recognized by an antibody against mouse CD40L. Moreover, it demonstrated functional activities on immature bone marrow dendritic cells by upregulating surface maturation markers (CD40, CD54, CD80, and CD86), and increasing IL-6 gene and protein expression. The availability of CD40L gene identity could greatly facilitate mechanistic research on pathogen-induced-immunopathogenesis and vaccine-elicited immune responses.
DOI:10.1101/337089