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This version published online on November 3, 2005
Endocrinology, doi:10.1210/en.2005-0715
A more recent version of this article appeared on February 1, 2006
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Submitted on June 15, 2005
Accepted on October 26, 2005

THE NEURONAL GROWTH ASSOCIATED PROTEIN GAP-43 IS EXPRESSED BY CORTICOTROPHS IN THE RAT ANTERIOR PITUITARY FOLLOWING ADRENALECTOMY

Charles M. Paden*, John A. Watt, Tiffany H. Selong, Courtney L. Paterson, and Harwood J. Cranston

Dept. of Cell Biology and Neuroscience (C.M.P., H.J.C.), Montana State University, Bozeman, MT 59717; Dept. of Anatomy and Cell Biology (J.A.W.), University of North Dakota, Grand Forks, ND 58203; Dept. of Anesthesiology (T.H.S.), University of North Carolina, Chapel Hill, NC 27599; and WWAMI Medical Education Program (C.M.P., C.L.P.), University of Washington School of Medicine, Seattle, WA 98195

* To whom correspondence should be addressed. E-mail: cpaden{at}montana.edu.

The neuronal growth associated protein GAP-43 has been localized both in long fibers and in punctate clusters by immunocytochemistry within the rat anterior pituitary (AP). Following adrenalectomy (ADX), GAP-43 immunoreactivity (GAP-43-ir) is greatly increased and is associated with corticotrophs at the light microscopic level. We have undertaken an electron microscopic study to determine the cellular localization of GAP-43 in the post-ADX AP. Using pre-embedding immunocytochemistry we found GAP-43-ir localized exclusively to the cytoplasmic surface of the plasmalemma within a subset of endocrine cells with ultrastructure typical of degranulated corticotrophs at 4 days post-ADX. We combined pre-embedding immunoelectron microscopy for GAP-43 with immunogold labeling for ACTH and found that GAP-43-ir was invariably present only in cells containing ACTH-positive granules. The density of GAP-43-ir was highest within extensive processes emanating from the soma, suggesting that these processes are the basis for the punctate clusters of GAP-43 staining seen surrounding corticotrophs in the light microscope. We also observed rare synaptic-like contacts between GAP-43-ir processes and distant cell bodies. GAP-43 mRNA was detected in extracts of the AP 4 days after ADX using RT-PCR, and quantitative PCR confirmed that GAP-43 mRNA was significantly upregulated in the AP in response to ADX. We postulate that increased expression of GAP-43 may stimulate process outgrowth and intercellular communication by activated corticotrophs.


Key words: corticotroph • GAP-43 • adrenalectomy • cell growth • ACTH







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