S. Uccini et al., KAPOSIS-SARCOMA CELLS EXPRESS THE MACROPHAGE-ASSOCIATED ANTIGEN MANNOSE RECEPTOR AND DEVELOP IN PERIPHERAL-BLOOD CULTURES OF KAPOSIS-SARCOMA PATIENTS, The American journal of pathology, 150(3), 1997, pp. 929-938
The mannose receptor (MR) is a surface 175-kd C-type lectin expressed
by macrophages and dendritic cells. MR is involved in removal of effet
e cells, phagocytosis of mannose-coated particles, pinocytosis, and an
tigen presentation. Expression of MR was investigated in 17 biopsies o
f Kaposi's sarcoma (3 AIDS KS, 13 classical KS, and 1 transplant-assoc
iated KS) using three anti-MR monoclonal antibodies (3.29, D547, and P
AM1). Immunostaining for MR was detected in 94 +/- 7% KS cells with sp
indle morphology. In normal tissues, MR was expressed by sinus-linking
cells of spleen and lymph nodes, but it was not detected in endotheli
al cells lining normal hematic and lymphatic vessels, hemangioma, hema
ngioendothelioma, and lymphangioma. Expression of MR in KS cells promp
ted us to investigate the possibility that they derive from a circulat
ing precursor cell. Peripheral blood mononuclear cells from 16 patient
s with KS (10 classical, 1 transplanted, and 5 AIDS) were cultured in
PHA-conditioned medium for 10 to 14 days. Confluent monolayers of adhe
rent spindle cells were detected in 8 of 11 classical KS, in 5 of 5 AI
DS KS patients, and in 0 of 34 control patients. Peripheral-blood-deri
ved KS-like cells were characterized by co-expression of macrophage an
d endothelial antigens being positive for CD45 (60%), CD68 (98%), MR (
70%), CD14 (25%), VE-cadherin (70%), and von Willebrand factor (10%).
When the immunophenotype of peripheral-blood-derived adherent cells wa
s compared with that of KS spindle cells of tissue biopsies, it was fo
und that both cell types are VE-cadherin(+)/MR(+)CD68(+), that periphe
ral-blood-derived spindle cells are CD34(-) and are less frequently st
ained for CD31 and von Willebrand factor, and that lesional KS cells d
o not express the leukocyte markers CD45 and CD18. Our findings are co
nsistent with the possibility that KS lesions derive from tissue accum
ulation and local proliferation of a special subset of macrophages wit
h endothelial features the normal counterpart of which are the sinus-l
ining cells of spleen and lymph nodes.