FASEB J.
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
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 EISENHOFER, G.
Right arrow Articles by HEARING, V. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by EISENHOFER, G.
Right arrow Articles by HEARING, V. J.
(The FASEB Journal. 2003;17:1248-1255.)
© 2003 FASEB

Tyrosinase: a developmentally specific major determinant of peripheral dopamine

GRAEME EISENHOFER*,1, HUA TIAN{dagger}, COURTNEY HOLMES*, JUN MATSUNAGA{ddagger}, SUZANNE ROFFLER-TARLOV§ and VINCENT J. HEARING{ddagger}

Sections on
* Clinical Neurocardiology and
{dagger} Neural Development, National Institute of Neurological Disorders and Stroke and
{ddagger} Laboratory of Cell Biology, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, USA; and
§ Departments of Neuroscience, Anatomy, and Cell Biology, Tufts University Medical School, Boston, Massachusetts, USA

1Correspondence: Building 10, Room 6N252, National Institutes of Health, 10 Center Dr. MSC 1620, Bethesda, MD 20892-1620, USA. E-mail: ge{at}box-g.nih.gov

L-3,4-dihydroxyphenylalanine, the immediate precursor of dopamine, can be formed by two enzymes: tyrosine hydroxylase (TH) in catecholamine-producing neurons and chromaffin cells and tyrosinase in melanocytes. In this study we examined whether tyrosinase contributes to production of dopamine. Deficiency of TH caused marked reductions in norepinephrine in albino and pigmented 15-day-old mice. In contrast, peripheral levels of dopamine were reduced only in albino TH-deficient mice and were higher in pigmented than in albino mice, regardless of the presence or absence of TH. We next examined age-related changes in dopamine and cutaneous expression of tyrosinase and melanin in albino and pigmented TH wild-type mice. We found that the differences in peripheral dopamine between pigmented and albino mice disappeared with advancing age following changes in expression and function of tyrosinase. In young animals, tyrosinase was present in epidermis but did not produce detectable melanin. With advancing age, tyrosinase was localized only around hair follicles, melanin synthesis became more pronounced, and dopamine synthesis decreased. The data reveal a previously unrecognized TH-independent major pathway of peripheral dopamine synthesis in young, but not adult, mice. The transient nature of this source of dopamine reflects a developmental switch in tyrosinase-dependent production of dopamine to production of melanin.—Eisenhofer, G., Tian, H., Holmes, C., Matsunaga, J., Roffler-Tarlov, S., Hearing, V. J. Tyrosinase: a developmentally specific major determinant of peripheral dopamine.


Key Words: L-dopa • tyrosine hydroxylase • sympathetic nervous system • melanocyte • melanin




This article has been cited by other articles:


Home page
Physiol. Rev.Home page
A. Slominski, D. J. Tobin, S. Shibahara, and J. Wortsman
Melanin Pigmentation in Mammalian Skin and Its Hormonal Regulation
Physiol Rev, October 1, 2004; 84(4): 1155 - 1228.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2003 by The Federation of American Societies for Experimental Biology.