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. 1997 Nov 11;94(23):12551–12556. doi: 10.1073/pnas.94.23.12551

Table 1.

Expression of surface molecules on HLA-DR+linIL-3RαhiDC from mononuclear tonsillar cells, PBMC, and fetal lymph node (LN) cells, and on CD34+IL-3Rαhi cells from fetal bone marrow (BM)

Tonsil Fetal LN PBMC Fetal BM
CD1a
CD3
CD4 ++/+++ ++/+++ ++ ++
CD5
CD11b
CD11c
CD13 −/+ + −/+ +
CD14
CD15 ND
CD16
CD19
CD20
CD32 + + + +
CD33 + +(+) +(+) +/++
CD34 −/+ + −/+ ++/+++
CD36 ++/+++* ++/+++ ++/+++ ++/++++
CD40 ++ + ++ +
CD45RA ++(+) ++(+) ++(+) ++
CD45RO
CD54 ++/+++ ND ++/+++ +/++
CD56
CD58 + ND +/++ +/++
CD62L + +/++ +++
CD64
CD80
CD86 + ND + +(+)
HLA-DR ++ ++ ++ ++
HLA-DQ ND −/+

Cells were stained as described in legends to Figs. 1, 3, and 4. Mean fluorescence intensity (MFI) levels for the IL-3Rαhi populations are expressed as −, indicating MFI in the first decade on a four log scale, which corresponds to isotype control levels. The +, ++, and +++ indicate MFI in the second, third, and fourth decades, respectively. A/sign means that MFI is on the border between two decades. Parenthesis means that the MFI is in the upper end of a decade. ND, not determined. The data are representative of at least three experiments. 

*

In one out of three experiments tonsillar HLA-DR+linIL-3RαhiDC were negative for CD36.