Abstract
New blood vessels develop from preexisting vessels in response to growth factors or
hypoxic conditions. Recent studies have shown that angiopoietin 2 (ANGPT-2) plays
an important role in the modulation of angiogenesis and vasculogenesis in humans and
mice. The signaling pathways that lead to the regulation of ANGPT-2 are largely unclear.
Here, we report that protein kinase C and protein kinase A activators (ADMB, 8-Cl-cAMP)
increased the mRNA levels of ANGPT-2 in human Granulosa cells, whereas PKC and PKA
Inhibitors (Rp-cAMP, GÖ 6983) decreased markedly the level of ANGPT-2 mRNA. Due to
varying specificity of the modulators for certain protein kinases subunits, we conclude
that the conventional PKCs, but not PKC α and β1, the atypical PKCs and the PKA I,
are involved in the regulation of ANGPT-2. These findings may help to explain the
role of both PKA and PKC dependent signaling cascades in the regulation of ANGPT-2
mRNA.
Key words
Protein kinase - Angiogenesis - ANGPT-2 - Corpus luteum
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D. Pietrowski, Ph. D.
Universitäts-Frauenklinik Freiburg
Hugstetter Str. 55 · 79106 Freiburg · Germany ·
Phone: + 49 (761) 270-3126
Fax: + 49 (761) 270-3037
Email: pietrowski@frk.ukl.uni-freiburg.de