Heterogeneous functional effects of concomitant B cell receptor and TLR stimulation in chronic lymphocytic leukemia with mutated versus unmutated Ig genes

Επιστημονική δημοσίευση - Άρθρο Περιοδικού uoadl:3001869 24 Αναγνώσεις

Μονάδα:
Ερευνητικό υλικό ΕΚΠΑ
Τίτλος:
Heterogeneous functional effects of concomitant B cell receptor and TLR stimulation in chronic lymphocytic leukemia with mutated versus unmutated Ig genes
Γλώσσες Τεκμηρίου:
Αγγλικά
Περίληψη:
We recently reported that chronic lymphocytic leukemia (CLL) subgroups with distinct clonotypic BCRs present discrete patterns of TLR expression, function, and/or tolerance. In this study, to explore whether specific types of BCR/TLR collaboration exist in CLL, we studied the effect of single versus concomitant BCR and/or TLR stimulation on CLL cells from mutated (M-CLL) and unmutated CLL (U-CLL) cases. We stimulated negatively isolated CLL cells by using anti-IgM, imiquimod, and CpG oligodeoxynucleotide for BCR, TLR7, and TLR9, respectively, alone or in combination for different time points. After in vitro culture in the absence of stimulation, differences in p-ERK were identified at any time point, with higher p-ERK levels in U-CLL versus M-CLL. Pronounced p-ERK induction was seen by single stimulation in U-CLL, whereas BCR/TLR synergism was required in M-CLL, in which the effect was overall limited in scale. An opposite pattern was observed regarding induction of apoptosis, as studied by Western blotting for the cleaved fragment of poly(ADP-ribose) polymerase, and the active isoform of caspase-8, with M-CLL responding even to single stimulation, contrasting with U-CLL that showed minimal response. Our findings suggest that concomitant engagement of BCR and TLR leads to differential responses in CLL depending on the mutational status of the BCR. Differential intensity and duration of responses in M-CLL versus U-CLL indicates that the differences in signal transduction between the two subgroups may be primarily quantitative rather than qualitative. Copyright © 2014 by The American Association of Immunologists, Inc.
Έτος δημοσίευσης:
2014
Συγγραφείς:
Chatzouli, M.
Ntoufa, S.
Papakonstantinou, N.
Chartomatsidou, E.
Anagnostopoulos, A.
Kollia, P.
Ghia, P.
Muzio, M.
Stamatopoulos, K.
Belessi, C.
Περιοδικό:
Journal of Immunological Methods
Εκδότης:
American Association of Immunologists
Τόμος:
192
Αριθμός / τεύχος:
10
Σελίδες:
4518-4524
Λέξεις-κλειδιά:
B lymphocyte receptor; caspase 8; CpG oligodeoxynucleotide; imiquimod; immunoglobulin heavy chain; isoprotein; mitogen activated protein kinase; nicotinamide adenine dinucleotide adenosine diphosphate ribosyltransferase; toll like receptor; toll like receptor 7; toll like receptor 9, apoptosis; article; chronic lymphatic leukemia; clinical article; controlled study; gene mutation; human; human cell; IGHV gene; immunoglobulin gene; immunostimulation; in vitro study; intracellular signaling; priority journal; protein cleavage; qualitative analysis; quantitative analysis; Western blotting, Adjuvants, Immunologic; Aged; Aged, 80 and over; Aminoquinolines; Caspase 8; Female; Humans; Immunoglobulins; Leukemia, Lymphocytic, Chronic, B-Cell; Male; Middle Aged; Mutation; Oligodeoxyribonucleotides; Receptors, Antigen, B-Cell; Signal Transduction; Toll-Like Receptor 7; Toll-Like Receptor 9
Επίσημο URL (Εκδότης):
DOI:
10.4049/jimmunol.1302102
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