IL-16 is a novel cytokine, which is chemoattractant for CD4(+) T cells
, macrophages, and eosinophils, Recently, it was reported that IL-16 i
s synthesized as an approximately 80-kDa precursor molecule, pro-IL-16
, Since little is known about the processing and tissue distribution o
f IL-16 and pro-IL-16, we investigated the distribution of IL-16 mRNA
and protein in human lymphoid tissue. Northern blotting identified IL-
16 mRNA predominantly in normal lymphoid organs, including PBMC, splee
n, and thymus, Immunohistochemistry of human lymph node localized IL-1
6 protein to lymphocyte cytoplasm within T cell zones and occasionally
in lymphocytes in B cell zones. Flow cytometric detection of intracel
lular IL-16 showed that >70% of CD4(+) and CD8(+) T cells constitutive
ly expressed IL-16 protein. Western blot analysis of PBMC revealed nea
rly all of this protein to be approximately 80-kDa pro-IL-16 in unstim
ulated PBMC, and upon cell activation, the amino terminus of pro-IL-16
is processed into multiple fragments. These results show that pro-IL-
16 is widely and constitutively expressed and suggest that the amino t
erminus of the protein can be processed upon cell activation.