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Vol. 280, Issue 1, 225-231, 1997
Third Department of Internal Medicine, Protein kinase C (PKC) is a Ca++- and
phospholipid-dependent protein kinase activated by diacylglycerol that
is either released from cell membranes in response to certain growth
factors or mimicked by 12-O-tetradecanoyl phorbol-13-acetate (TPA). We
studied the effects of TPA on interleukin-3 (IL-3)-dependent colony
formation of mouse bone marrow cells from mice injected with
5-fluorouracil 2 days before examination in order to clarify the
significance of PKC in the proliferation of primitive hematopoietic
progenitors. Although TPA alone did not support colony formation, TPA
in combination with IL-3 increased colony numbers from 1.5 to 2 times
that formed with IL-3 and vehicle. TPA increased not only the
granulocyte/macrophage colonies, but also the multilineage colonies. A
sequential colony count showed that TPA, unlike IL-6, did not hasten
the appearance of colonies. Because TPA enhanced IL-3-dependent colony
formation derived from lineage-negative marrow cells obtained from mice that received 5-FU 2 days before, it is possible that it might act
directly on primitive progenitors. Prolonged pretreatment of marrow
cells with TPA prevented TPA-augmented colony growth. Calphostin C, a
specific PKC inhibitor, and certain specific tyrosine kinase
inhibitors, such as genistein and herbimycin A, abrogated the enhancing
effects of TPA on IL-3-dependent colony formation. These data suggest
that TPA had a direct effect on the primitive progenitors and enhanced
IL-3-dependent colony formation via activation of PKC and
certain tyrosine kinases.
Copyright © by The American Society for Pharmacology and Experimental Therapeutics
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