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Journal of Cell Science 115, 1313-1320 (2002)
© 2002 The Company of Biologists Limited


Research Article

Activation of protein kinase C{eta} triggers cortical granule exocytosis in Xenopus oocytes

Cameron B. Gundersen*, Sirus A. Kohan, Qian Chen, Joseph Iagnemma and Joy A. Umbach

Department of Molecular & Medical Pharmacology, UCLA School of Medicine, Los Angeles, CA 90095, USA

* Author for correspondence (e-mail: cgundersen{at}mednet.ucla.edu )

Accepted 12 December 2001

Previous work has shown that phorbol esters or diacylglycerol trigger cortical granule exocytosis in Xenopus oocytes. We sought to identify the isoform(s) of protein kinase C (PKC) that mediate(s) this regulated secretory event. Because this process is initiated by lipid activators of PKC but is independent of calcium ions, we focused on the family of novel (calcium-independent) PKCs. Pharmacological investigations using Gö6976 and Gö6983 tended to exclude PKC{delta}, {epsilon} and µ as secretory triggers. Subcellular fractionation and immunoblot data revealed that these oocytes expressed all five members of the novel PKC family, but it was only PKC{eta} that colocalized with cortical granules. Finally, expression of wild type or constitutively active forms of PKC{delta} and {eta} strongly supported the conclusion that it is PKC{eta} that initiates cortical granule exocytosis in these cells. These observations represent an important step in identifying the mechanism of secretory triggering in this system.

Key words: Secretion, Cortical reaction, protein kinase C


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