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* INSERM U311, Etablissement de Transfusion Sanguine, 67065 Strasbourg;
INSERM U151, CHU Rangueil, 31054 Toulouse;
Wilson Hall, University of Alabama in Huntsville, Alabama 35899, USA; and
§ Laboratoire D'Immunologie, CHU Rangueil, 31054 Toulouse Cedex, France
1Correspondence: INSERM U311, Etablissement de Transfusion Sanguine, 67065 Strasbourg Cedex, France. E-mail: jason.hatton{at}etss.u-strasbg.fr
Protein kinase C (PKC) is a family of serine/threonine kinases that play
an important role in mediating intracellular signal transduction in
eukaryotes. U937 cells were exposed to microgravity during a space
shuttle flight and stimulated with a radiolabeled phorbol ester
([3H]PDBu) to both specifically label and activate
translocation of PKC from the cytosol to the particulate fraction of
the cell. Although significant translocation of PKC occurred at all
g levels, the kinetics of translocation in flight were
significantly different from those on the ground. In addition, the
total quantity of [3H]PDBu binding PKC was increased in
flight compared to cells at 1 g on the ground, whereas the
quantity in hypergravity (1.4 g) was decreased with respect
to 1 g. Similarly, in purified human peripheral blood T
cells the quantity of PKC
varied in inverse proportion to the
g level for some experimental treatments. In addition to
these novel findings, the results confirm earlier studies which showed
that PKC is sensitive to changes in gravitational acceleration. The
mechanisms of cellular gravisensitivity are poorly understood but the
demonstrated sensitivity of PKC to this stimulus provides us with a
useful means of measuring the effect of altered gravity levels on early
cell activation events.Hatton, J. P., Gaubert, F., Lewis,
M. L., Darsel, Y., Ohlmann, P., Cazenave, J.-P., Schmitt, D. The
kinetics of translocation and cellular quantity of protein kinase C in
human leukocytes are modified during spaceflight.
Key Words: microgravity translocation
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