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Volume 271, Number 26,
Issue of June 28, 1996
pp. 15346-15352
©1996 by The American Society for Biochemistry and Molecular Biology, Inc.
Auto-regulation of Retinoic Acid Biosynthesis through Regulation
of Retinol Esterification in Human Keratinocytes
(Received for publication, January 25, 1996, and in revised form, April 2, 1996)
Sara B.
Kurlandsky
,
Elizabeth A.
Duell
,
Sewon
Kang
,
John J.
Voorhees
and
Gary J.
Fisher
From the Department of Dermatology, University of Michigan, Ann
Arbor, Michigan 48109-0528
In this report, we describe an auto-regulatory
loop in human keratinocytes, whereby all-trans retinoic
acid (retinoic acid) regulates its own biosynthesis from
all-trans retinol (retinol) through regulation of retinol
esterification. Retinol esterification activity was low in normal
proliferating human keratinocytes, cultured in retinoid-free media.
Treatment of keratinocytes with retinoic acid induced retinol
esterifying activity (8-fold). Induction of retinol esterifying
activity was blocked by either actinomycin D or cycloheximide. Based on
substrate specificity and inhibitor sensitivity, lecithin:retinol
acyltransferase (LRAT) was identified as the retinoic acid-inducible
retinol esterifying enzyme. Induction of LRAT by retinoic acid reduced
conversion of retinol to retinoic acid by 50%. This reduction in
retinoic acid synthesis resulted from sequestration of retinol as
retinyl esters, since inhibition of LRAT restored retinoic acid
synthesis to control levels. In normal human skin, undifferentiated
keratinocytes, in the lowest cell layer, esterified retinol 4 times
greater, than differentiating keratinocytes, in upper cell layers,
reflecting an induced state, under conditions of retinol sufficiency.
Regulation of LRAT activity by retinoic acid provides a novel mechanism
through which retinoic acid can regulate its own level by controlling
availability of retinol for conversion to retinoic acid. In human skin
in vivo, retinyl esters synthesized in basal keratinocytes
could undergo hydrolysis during differentiation and thus serve as a
source of retinol for keratinocytes in upper layers of skin.

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Copyright © 1996 by the American Society for Biochemistry and Molecular Biology.
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