| |
|
|
|
INTRODUCTION
|
|
The fur of mink (Mustela
vison) consists of an outer layer of sparse, but large
guard hairs and a dense inner layer of short, thin underhair fibers,
the latter of which comprise over 95% of the fur. Hair follicles
develop as bundles, with all hairs of a bundle emerging through a common
opening in the skin (Figs 1 & 2). The most prevalent bundles are:
G-type, containing a large guard hair follicle and a variable number of underhair
follicles, I-type, composed of an intermediate size guard hair follicle and
variable number of underhair follicles and, U-type, with under hair follicles
only. Bundles most often occur in trio-arrangements of G-I-I or G-U-U.
Fig. 1 The three hair follicle bundle
types in mink are: G-type, containing a single large guard hair follicle
plus a variable number of underhair follicles, I-type, containing a
single, intermediate size guard hair follicle, plus a variable number of
underhair follicles, and U-type, with underhair follicles only.
Fig. 2: (Top): Computer generated drawings
of G-U-U and G-I-I trio-arrangement of hair follicle bundles.
(Bottom): Light-micrographs of same in anagen. The small arrow
indicates an old follicle while the large arrow indicates a follicle in
anagen.
In the spring, increasing photoperiod and serum prolactin
(PRL) levels are correlated with onset of the growing (anagen) phase of the
summer hair growth cycle and molting of winter fur. Hair growth continues
until early-summer when all follicles undergo a short, apoptotic-driven regression
(catagen) resulting in the resting (telogen) phase of the hair cycle. Follicles
remain inactive until early-fall when decreasing photoperiod and serum PRL
levels result in onset of the winter hair growth cycle and molting of summer
fur. Hair growth continues until mid-Dec when all follicles progress through
catagen, to telogen and remain inactive until the following spring.
During the development of the winter pelage, there is a 40% or greater
increase in the number of derived under hair follicles that become active,
compared to summer anagen. This is of interest because mammals appear to
develop all of their hair follicles by birth, or shortly thereafter. Thus,
a major challenge will be: To determine why all of the "available" under
hair follicles are not activated during summer anagen. Conversely, we need
to determine the nature of the endocrine signals that results in activation
of those hair follicles during winter anagen, that were inactive during summer
anagen.
Prolactin (PRL) has long been suspected to play a role in hair growth
cycles of mammals, especially those that exhibit seasonal changes in pelage
such as sheep, Djungarian hamsters and mink. Recently, PRL has received
increased attention as a potential modulator of rodent and human hair growth
cycles (Foitzik et al., 2003; Craven et al., 2001). It is intriguing however,
that PRL has both stimulatory and inhibitory effects on hair growth, that
are dependent on species and perhaps even season of the year. For example,
in mice and humans PRL reduces hair growth rate, blocks anagen and promotes
a catagen-like transformation of follicles in vitro. In contrast, PRL
appears to stimulate the onset of summer fur growth, and perhaps inhibit the
development of winter fur in Djungarian hamsters and mink.
Thus, our objectives were to determine the effects of PRL on:
(1): initiation of spontaneous & depilation-induced
anagen, and
(2): hair fiber density, diameter, cross-sectional area,
& ellipticity
BACK TO POSTER
|
|
|
|