Acute myeloblastic leukaemia cells produce soluble interleukin 6 receptor by a mechanism of alternative splicing

Citation
M. Saily et al., Acute myeloblastic leukaemia cells produce soluble interleukin 6 receptor by a mechanism of alternative splicing, CYTOKINE, 10(11), 1998, pp. 860-867
Citations number
48
Categorie Soggetti
Cell & Developmental Biology
Journal title
CYTOKINE
ISSN journal
10434666 → ACNP
Volume
10
Issue
11
Year of publication
1998
Pages
860 - 867
Database
ISI
SICI code
1043-4666(199811)10:11<860:AMLCPS>2.0.ZU;2-A
Abstract
The aim of the present work was to investigate whether acute myeloblastic l eukaemia (AML) blast cells express a soluble (s) form of interleukin 6 (IL- 6) receptor (R), and if they do, what is the mechanism of production. Eight AML patient cell lines and 25 primary AML blast cell samples were investig ated. The cell lines secreted high quantities of sIL-6R into their culture medium when examined by enzyme-linked immunosorbent assay (ELISA), To deter mine whether sIL-6R is synthesized by a mechanism of alternative splicing, RNA was analysed from all the AML, blast cell samples by using reverse tran scription polymerase chain reaction. In this method, primer sites flanking the transmembrane domain were utilized and the alternatively spliced IL-6R mRNA was distinguished from the non-spliced transcript form by size. All th e cell lines and 64% of the primary blast cell samples expressed the altern atively spliced IL-6R mRNA, To confirm the phenomenon of alternative splici ng at protein level, cytoplasmic protein fractions of the cell Lines were i nvestigated by using a sensitive adaptation of the Western blot method. All the cell lines expressed two IL-6R proteins sized 80 and 56 kDa and corres ponding to the membraneous and soluble forms of IL-6R, respectively. In conclusion, the results obtained at both mRNA and protein levels strongl y support alternative splicing as a mechanism of sIL-6R production in AML, Because sIL-6R modulates the effects of IL-6 on target cells, differences i n sIL-6R expression levels may partially explain the previously observed di versity in IL-6-induced growth responses in AML, (C) 1998 Academic Press.