Autor: |
Benitez, Abigail, Weldon, Abby J., Tatosyan, Lynnette, Velkuru, Vani, Lee, Steve, Milford, Terry-Ann, Francis, Olivia L., Hsu, Sheri, Nazeri, Kavoos, Casiano, Carlos M., Schneider, Rebekah, Gonzalez, Jennifer, Su, Rui-Jun, Baez, Ineavely, Colburn, Keith, Moldovan, Ioana, Payne, Kimberly J. |
Jazyk: |
angličtina |
Rok vydání: |
2014 |
Předmět: |
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Popis: |
Identifying cross-species similarities and differences in immune development and function is critical for maximizing the translational potential of animal models. Coexpression of CD21 and CD24 distinguishes transitional and mature B cell subsets in mice. In this study, we validate these markers for identifying analogous subsets in humans and use them to compare the nonmemory B cell pools in mice and humans, across tissues, and during fetal/neonatal and adult life. Among human CD19(+)IgM(+) B cells, the CD21/CD24 schema identifies distinct populations that correspond to transitional 1 (T1), transitional 2 (T2), follicular mature, and marginal zone subsets identified in mice. Markers specific to human B cell development validate the identity of marginal zone cells and the maturation status of human CD21/CD24 nonmemory B cell subsets. A comparison of the nonmemory B cell pools in bone marrow, blood, and spleen in mice and humans shows that transitional B cells comprise a much smaller fraction in adult humans than mice. T1 cells are a major contributor to the nonmemory B cell pool in mouse bone marrow, in which their frequency is more than twice that in humans. Conversely, in spleen, the T1:T2 ratio shows that T2 cells are proportionally ∼ 8-fold higher in humans than in mice. Despite the relatively small contribution of transitional B cells to the human nonmemory pool, the number of naive follicular mature cells produced per transitional B cell is 3- to 6-fold higher across tissues than in mice. These data suggest differing dynamics or mechanisms produce the nonmemory B cell compartments in mice and humans. |
Databáze: |
OpenAIRE |
Externí odkaz: |
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