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1 Institute of Bioengineering, Miguel Hernandez University, 03550 San Juande Alicante, Spain; 2 Department of Morphology, University of Geneva, 1211 Geneva 4, Switzerland; and 3 Department of Surgery, National University of Singapore, National University Hospital, Singapore 119074
Pancreatic
-cells constitute a
well-communicating multicellular network that permits a coordinated and
synchronized signal transmission within the islet of Langerhans that is
necessary for proper insulin release. Gap junctions are the molecular
keys that mediate functional cellular connections, which are
responsible for electrical and metabolic coupling in the majority of
cell types. Although the role of gap junctions in
-cell electrical coupling is well documented, metabolic communication is still a matter
of discussion. Here, we have addressed this issue by use of a
fluorescence recovery after photobleaching (FRAP) approach. This
technique has been validated as a reliable and noninvasive approach to
monitor functional gap junctions in real time. We show that control
pancreatic islet cells did not exchange a gap junction-permeant
molecule in either clustered cells or intact islets of Langerhans under
conditions that allowed cell-to-cell exchange of current-carrying ions.
Conversely, we have detected that the same probe was extensively
transferred between islet cells of transgenic mice expressing connexin
32 (Cx32) that have enhanced junctional coupling properties. The
results indicate that the electrical coupling of native islet cells is
more extensive than dye communication. Dye-coupling domains in islet
cells appear more restricted than previously inferred with other methods.
islets of Langerhans; gap junctions; intercellular communication
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