Two populations of B lymphocytes, B-l (CD5(+) and/or CD11b(+)) and B-2
(CD5(-) and CD11b(-)) cells have been described. In mice, which is th
e species of reference for B-l and B-2 cell studies, these two subsets
present different developmental schemes, phenotypes, antibody reperto
ires, localization and behaviours. Interestingly, in sheep, B cells re
arrange their immunoglobulin (Ig) loci around the neonatal period, sim
ilarly to murine B-l cells. However, the phenotype of the sheep B cell
s has not been characterized with regards to their developmental pathw
ay. In this report, we show that two sheep B-cell subsets can be disti
nguished on the basis of CD11b expression. Relative to CD11b(-) B cell
s, the CD11b(+) B cells frequently co-express CD5, CD11c, higher level
s of surface IgM (sIgM), show larger cell size and higher cell-cycling
activity, and thus present a B-l-like phenotype. However, unlike muri
ne B-l cells, sheep B-l like cells mainly localize in blood, display a
higher propensity to spontaneous apoptosis relative to B-2-like cells
, and proliferate after sIgM stimulation. Our data show that despite n
eonatal immunoglobulin loci rearrangements, sheep B cells do not all e
xpress a B-l-like phenotype. However, B-l-and B-2-like cells co-exist
and present phenotypic and behavioural specificities. Nevertheless, sh
eep B-l-and B-2-like cells differ from the murine B-l and B-2. cells i
n their cell behaviour. These subsets can thus not be considered as tr
ue homologues among species.