G. Graf et al., EXPRESSION OF THROMBOPOIETIN AND THROMBOPOIETIN RECEPTOR MPL IN HUMANLEUKEMIA-LYMPHOMA AND SOLID TUMOR-CELL LINES, Leukemia research, 20(10), 1996, pp. 831-838
Thrombopoietin (TPO) is the major regulator of platelet production in
vivo and is the ligand for the MPL receptor. In an effort to determine
the distribution of TPO and MPL in the different hematopoietic cell t
ypes and in various types of tissue, we examined the mRNA expression o
f this ligand-receptor pair in two series of human leukemia-lymphoma c
ell lines and of solid tumor cancer cell lines using northern blot and
reverse transcriptase-polymerase chain reaction (RT-PCR) analysis. At
the northern blot mRNA level, 8/15 (53%) megakaryocytic and 3/11 (27%
) erythroid leukemia cell lines expressed MPL mRNA; except for one pos
itive monocytic cell line, the remaining 78 pre B-cell, B-cell, plasma
cell, T-cell, NK cell, myeloid, monocytic and Hodgkin/anaplastic larg
e cell lymphoma (ALCL)-derived cell lines were negative. No MPL messag
e was detected in any of the 23 solid tumor cell lines established fro
m 21 different tumors. In order to examine whether a low level of MPL
expression could be detected, 51 leukemia cell lines were investigated
with the RT-PCR technique. By this technique, MPL message was seen in
many more cell types: 13/26 (50%) of non-erythro-megakaryocytic cell
lines and in nearly all megakaryocytic (14/15, 93%) and erythroid (10/
11, 91%) cell lines. Thus, the highest expression of MPL clearly occur
s in cells with megakaryocytic differentiation; furthermore, expressio
n of MPL appears to be restricted to hematopoietic cell types. TPO mRN
A expression was examined by RT-PCR and found in 9/11 (82%) of the sol
id tumor cell lines (derived from colon, endometrium, kidney, liver, o
vary, retinoblastoma and urinary bladder cancers). Among the leukemia-
lymphoma cell lines, TPO mRNA was detected by RT-PCR in most plasma ce
ll, myeloid, megakaryocytic and erythroid cell lines, but not in pre B
-cell, B-cell or T-/NK-cell lines. The results reported here extend th
e observations of MPL and TPO expression in normal cells to the whole
spectrum of hematological cell types and to an array of different tiss
ue types, both exemplified by their malignant counterparts. Copyright
(C) 1996 Elsevier Science Ltd