L. Alibardi et Mb. Thompson, Fine structure of the developing epidermis in the embryo of the American alligator (Alligator mississippiensis, Crocodilia, Reptilia), J ANAT, 198, 2001, pp. 265-282
The morphological transition from the simple epidermis that contacts the am
niotic fluid of embryonic crocodilians to the adult epidermis required in a
terrestrial environment has never been described. We used light and electr
on microscopy to study the development, differentiation and keratinisation
of the epidermis of the American alligator, Alligator. mississippiensis, be
tween early and late stages of embryonic skin formation. In early embryonic
development, the epidermis consists of a flat bilayer. As it develops, the
bilayered epidermis comes to lie beneath the peridermis. Glycogen is almos
t absent from the bilayered epidermis but increases in basal and suprabasal
cells when scales form. Glycogen disappears from suprabasal cells that acc
umulate keratin. The peridermis and 1 or 2 subperidermal layers form an emb
ryonic epidermis that is partially or totally lost before hatching. These c
ells accumulate coarse filaments and form reticulate bodies. Mucous and lam
ellate granules are produced in the Golgi apparatus and are partly secreted
extracellularly. The embryonic cells darken with the formation of larger r
eticulate bodies that aggregate with intermediate filaments and other cell
organelles, as their nuclear chromatin condenses. Thin beta -cells resembli
ng those of scutate scales of birds develop beneath the embryonic epidermis
and form a stratified beta -layer that varies in thickness in different bo
dy regions. The epidermis differentiates first in the back, tail and belly.
At the beginning of beta -cell differentiation, the cytoplasm contains spa
rse bundles of alpha -keratin filaments, glycogen and lipid droplets or vac
uoles apparently derived from the endoplasmic reticulum and Golgi apparatus
. These organelles disappear rapidly as irregular bundles of electron-dense
beta -keratin filaments accumulate and form larger bundles. The larger bun
dles consist of 3 nm thick electron-pale keratin microfibrils and are deriv
ed from the assemblage of beta -keratin molecules produced by ribosomes. Wh
ile in mammals the epidermal barrier is formed by alpha -keratinocytes, in
the alligator the barrier is formed by alpha -keratin cells. The beta -laye
r is reduced or absent from the small hinge region between scales. In the l
atter areas the barrier is made of or a mixture of alpha/beta keratinocytes
. Thus alligators resemble birds where the beta -keratin molecules are depo
sited directly over alpha -keratin scaffold, rather than an initial product
ion of beta -keratin packets which then merge with alpha -keratin, as occur
s in the Chelonia and Lepidosauria. The pigmentation of the epidermis of em
bryos is mostly derived from epidermal melanocytes.