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1- and ß1-Adrenergic Modulation of Lacrimal Gland Function in the Mouse1From the Department of Cell and Neurobiology, University of Southern California, Los Angeles, California; the 2Department of Neurobiology and Behavior, State University of New York at Stony Brook, Stony Brook, New York; the 3Vision Science Centre RSBS, Australian National University, Canberra, ACT, Australia; and the 4Vision Science Research Center, University of Alabama at Birmingham, Birmingham, Alabama.
PURPOSE. To determine the expression patterns of
1- and ß1-adrenergic receptors in the mouse exorbital lacrimal gland (LG). An
- and ß-receptor agonist and antagonist were used to elucidate the receptors relevance to protein secretion.
METHODS. Mouse LGs were processed for single- and double-labeled indirect immunofluorescence studies and examined with confocal scanning microscopy. Protein secretion was measured from gland fragments in response to adrenergic agonists.
RESULTS. Extensive
1-immunoreactivity (IR) was found on the surface and cytoplasm of acinar cells and much more
1-IR in the interstitial areas. In contrast, more ß1-IR was found in the LG, and most ß1-IR appeared to concentrate in the cytoplasm of acinar cells, with almost no ß1-IR in the interstitial areas. The protein secretion in response to phenylephrine and isoproterenol showed that direct stimulation of either the
1- or ß1-receptor could induce significant protein secretion from LGs. The specificity of this stimulation was further indicated by the effects of adrenergic antagonists. No synergism was observed between
1- and ß-receptor-mediated protein secretions.
CONCLUSIONS. The results support the notion that there is extensive adrenergic control in the mouse LG. The adrenergic receptors may be a better choice of markers, compared with tyrosine hydroxylase and dopamine ß-hydroxylase, to reflect the extent of adrenergic control because circulating norepinephrine in the bloodstream should be taken into consideration. Both confocal microscopy observations and protein secretion data suggest the presence of
1- and ß1-mediated pathways in the mouse LG.
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