IOVS
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Originally published In Press as doi:10.1167/iovs.08-2467 on September 29, 2008
(Investigative Ophthalmology and Visual Science. 2009;50:614-620.)
© 2009 by The Association for Research in Vision and Ophthalmology, Inc.
doi:10.1167/iovs.08-2467

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
iovs.08-2467v1
50/2/614    most recent
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Shatos, M. A.
Right arrow Articles by Dartt, D. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Shatos, M. A.
Right arrow Articles by Dartt, D. A.

Role of cPKC{alpha} and nPKC{epsilon} in EGF-Stimulated Goblet Cell Proliferation

Marie A. Shatos,1 Robin R. Hodges,1 Yoshia Oshi,1 Jeffrey A. Bair,1 Driss Zoukhri,2 Claire Kublin,2 Kameran Lashkari,1 and Darlene A. Dartt1

1From the Schepens Eye Research Institute and Department of Ophthalmology, Harvard Medical School, Boston, Massachusetts; and 2Tufts University School of Dental Medicine, Boston, Massachusetts.

PURPOSE. The authors determined the role of the protein kinase C (PKC) isoforms cPKC{alpha} and nPKC{epsilon} in EGF-stimulated proliferation of cultured rat and human conjunctival goblet cells.

METHODS. Rat and human conjunctivas were minced, and goblet cells were allowed to grow. Passage 1 cells were serum starved for 24 to 48 hours and were incubated with the PKC inhibitors calphostin C and Gö 6983 (10–10-10–7 M) for 20 minutes before stimulation with EGF (10–7 M) for 24 hours. The presence and localization of PKC isoforms in cultured rat goblet cells were determined by Western blot analysis and immunofluorescence microscopy, respectively. Cultured rat goblet cells were serum starved and incubated with adenoviruses containing genes for dominant-negative cPKC{alpha} (Ad DNPKC{alpha}, 104 pfu), dominant-negative nPKC{epsilon} (Ad DNPKC{epsilon}, 104 pfu), and wild-type cPKC{alpha} (Ad WTPKC{alpha}, 107 pfu), and proliferation was measured.

RESULTS. In rat goblet cells, EGF-stimulated proliferation was completely inhibited by calphostin C, whereas Gö 6983 inhibited proliferation by 53% ± 15%. In human goblet cells, EGF-stimulated proliferation was completely inhibited by calphostin C. PKC{alpha}, -βI, -βII, -{delta}, -{epsilon}, -{iota}/{lambda}, -{theta}, -{gamma}, and -{zeta} were found in cultured rat goblet cells. Ad DNPKC{alpha} and Ad DNPKC{epsilon} inhibited EGF-stimulated proliferation in rat goblet cells by 78% ± 6% and 92% ± 8%, respectively. Incubation with Ad WTPKC{alpha} alone significantly increased proliferation.

CONCLUSIONS. cPKC{alpha} and nPKC{epsilon} play key roles in conjunctival goblet cell proliferation.





This article has been cited by other articles:


Home page
J. Biol. Chem.Home page
M. M. Wouters, J. L. Roeder, V. S. Tharayil, J. E. Stanich, P. R. Strege, S. Lei, M. R. Bardsley, T. Ordog, S. J. Gibbons, and G. Farrugia
Protein Kinase C{gamma} Mediates Regulation of Proliferation by the Serotonin 5-Hydroxytryptamine Receptor 2B
J. Biol. Chem., August 7, 2009; 284(32): 21177 - 21184.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2009 by the Association for Research in Vision and Ophthalmology