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Am J Physiol Cell Physiol (September 18, 2002). doi:10.1152/ajpcell.00160.2001
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Articles in PresS, published online ahead of print September 18, 2002
Am J Physiol Cell Physiol, 10.1152/ajpcell.00160.2001
Submitted on March 28, 2001
Accepted on September 11, 2002

Signal transduction of somatostatin in human B lymphoblasts

Dieter Rosskopf1*, Markus Schurks1, Iris Manthey1, Markus Joisten1, Stefan Busch1, and Winfried Siffert1

1 Institut fuer Pharmakologie, Universitaetsklinikum Essen, Essen, Germany

* To whom correspondence should be addressed. E-mail: dieter.rosskopf{at}uni-essen.de.

Somatostatin (SST) and somatostatin receptors (SSTR) are widely distributed in lymphoid tissues. Here we report on stimulatory effects of SST in Epstein-Barr virus-immortalized B lymphoblasts. By RT-PCR, we demonstrated the exclusive expression of the somatostatin receptor isoform 2A (SSTR2A) in B lymphoblasts. Addition of SST rapidly increased the cytosolic free calcium concentration, [Ca2+]i, maximally by about 200 nM with an EC50 of 1.3 nM, and stimulated the formation of inositol phosphates. Furthermore, SST increased binding of guanosine 5'-{gamma}-thio triphosphate by 50% above basal. These effects were partly inhibited by pertussis toxin (PTX), which indicates the involvement of PTX-sensitive G proteins. We provide further evidence that G{alpha}16, a PTX-insensitive G protein confined to lympho-hematopoietic cells, is involved in the otherwise unusual coupling of SSTR2A to phospholipase C activation. In addition, SST activated extracellular regulated kinases and induced a 3.5-fold stimulation of DNA synthesis and a 4.4-fold stimulation of B lymphoblast proliferation which was accompanied by an enhanced immunoglobulin formation. Thus, SST exerts a growth factor-like activity on human B lymphoblasts.




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