The D-type cyclins, involved in the regulation of G(1) progression of the c
ell cycle, are expressed in a lineage-specific manner. Normal hematopoietic
cells express cyclin D2 and/or D3. In order to determine whether their exp
ression pattern changes in lymphoid tumors, we examined cyclin D2 and D3 ex
pression in non-neoplastic and neoplastic lymphoid lesions, using a sensiti
ve immunohistochemical amplification method. Centroblasts in lymphoid folli
cles of reactive lymph nodes expressed exclusively cyclin D3 and no D2. Int
erfollicular areas contained scattered cyclin D3 and D2 positive cells. By
double staining, cyclin D3 was detected in CD79a positive B cells, CD3 posi
tive T cells and CD68 positive macrophages. Cyclin D2 was present only in C
D3 positive T cells. Neoplastic lymphoid lesions included 33 B cell lymphom
as, 9 T cell lymphomas and 12 Hodgkin's lymphomas. The B cell lymphomas com
prised 9 follicular lymphomas (FL), I Burkitt lymphoma (BL), 22 diffuse lar
ge cell lymphomas (DL) and chronic lymphocytic leukemia (CLL). All 9 FLs an
d the single BL expressed exclusively cyclin D3, similarly to germinal cent
er B cells, that represent their cells of origin. Six DLs expressed both cy
clin D2 and D3, while 6 expressed only D3. Among the 9 pleomorphic T cell l
ymphomas, medium and large cell type, 5 expressed cyclin D2. Cyclin D3 was
also detected in scattered cells in 4 of 9 cases and was highly expressed i
n 2 of 9 T cell lymphomas. The majority of Hodgkin's lymphomas expressed bo
th cyclin D2 and D3 in Hodgkin/Reed-Sternberg (HRS) cells. The high frequen
cy of positive cells indicates that both cyclins were expressed in the same
cells. (C) 1999 Wiley-Liss, Inc.