The
integumentary system (integument, a covering) consists of the skin (cutis) and
its appendages. The protective covering
for the body known as the skin is one of the largest organs of the body and
accounts for approximately 16% of the body weight. It contains glands, blood vessels, lymphatic vessels, nerves, and
smooth muscle (arrector pili muscles).
The appendages are derived from the overlying epidermis and include two
types of sweat glands, sebaceous glands, hair, and nails.
The
skin has two defining tissue types, epidermis
(keratinocytes are derived from ectoderm) and dermis (derived from mesoderm).
The dermis interfaces with the underlying hypodermis, which is the fatty subcutaneous connective tissue or
the superficial fascia of gross anatomy.
Although the hypodermis not officially considered to be one of the
layers of the skin, it is a loose connective tissues that attaches the skin to
underlying tissues by way of vertical septae and permits skin mobility over
most parts of the body (e.g., when it is pinched up), it serves as an insulator
and shock absorber and serves as a caloric reservoir.
Skin
is often classified as either thick skin
or thin skin. This classification refers to epidermal
thickness rather than dermal thickness or to the thickness of the skin as a
whole. Thick skin (= thick epidermis) is restricted to palms and soles. Thin skin (= thin epidermis) covers the
remainder of the body. Although skin
may have a very thick dermis in some sites, as on the back, it is classified as
thin skin if the epidermis is thin.
Skin
has many functions, some of which can be appreciated from the study of its
microscopic structure. As the covering
of the body, the skin provides some protection
from injury, and from the entry of microorganisms. Protection is also provided by the melanocytes, which produce
pigment to shield the body from too much ultraviolet light. The skin functions in temperature
regulation, e.g., by sweating, varying peripheral blood flow. It covers the surface with sebum to
lubricate the epidermal surface and prevent cracking. The adipose tissue of the hypodermis provides insulation. The skin also functions in excretion (and secretion) via its sweat
and sebaceous glands. Moreover, it stores fat, manufactures vitamin D and is the first guard of the immunosurveillance system. Cutaneous receptors for touch, pressure,
heat, and pain stimuli provide a sensory appreciation of the environment; thus
the skin serves as a sensory organ. The skin acts as a friction surface for motor tasks involving grasping, rubbing,
scratching, etc. The skin is also
important in preventing the loss of body
fluids, a fact that is well illustrated when excessive fluid loss occurs
after extensive burns.
Study the section of
thick skin on Slides A99 (H & E) or BB-41 and identify the
layers of the epidermis: stratum basale,
stratum spinosum, stratum granulosum, and stratum corneum. See Figure
55 below. The predominant cell type, an
epidermal keratinocyte begins its life cycle in the basal layer and becomes
progressively more differentiated as it moves toward the surface - a process
that produces a stratified squamous keratinizing epithelium.
Observe the flattened, dead surface cells (sometimes called corneocytes or dandruff in the scalp) of the thick stratum corneum. A few of the surface cells are being desquamated. Some areas of the stratum corneum show spiraling sweat ducts, each of which will end in a sweat pore at the surface. Nuclei and other cellular organelles are absent in the stratum corneum.

Figure 55: Micrograph of thick skin. C = stratum corneum, G = stratum granulosum,
S = stratum spinosum and B = stratum basale.
Taken from Wheater’s Functional Histology, a text and colour atlas,
p. 158, Figure 9.2.
The
stratum granulosum is composed of
increasingly flattened rectangular-shaped cells filled with keratohyalin granules. The large accumulation of basophilic
granules in these cells is composed of filaggrin and keratin filaments. The thickness of this layer varies from one
to three cells and as a rule is representative of the rate of
keratinization. Thus, there are little
or no stratum granulosum or keratohyalin granules in diseases, with a rapid
rate of keratinization such as psoriasis, whereas the granular layer is
thickened in diseases with a slow rate of keratinization.
The
stratum spinosum is composed of
several layers of polyhedral cells, which flatten as the stratum granulosum is
approached. See Figure 56 below. The cytoplasm is rich in tonofibrils, which
are specific for keratin pairs 1 and 10.
Individual cells appear to be separated by spaces that are traversed by
the so-called intercellular bridges
which, under oil immersion, can be seen as fine lines between adjacent cells. They account for the prickly appearance of
the cells and for their frequent designation as prickle cells. These are tissue preparation artifacts
caused when water is removed during the dehydration step. Spinous cells are attached to their
neighbors by a multitude of desmosomal attachments and these connections remain
as the fragile cytoplasm shrinks.

Figure 56: Micrograph of the
keratinocytes of the stratum spinosum. Taken
from Wheater’s Functional Histology, a text and colour atlas, p. 159, Figure
9.4c.
The
stratum basalis is composed of a
single layer of cuboidal to columnar cells, which are attached to the basement
membrane by hemidesmosomes. These cells
express keratin intermediate filament pairs 5 and 14. This layer contains the stem cell population and an occasional
mitotic figure of a transient amplifying cell may be observed. A few melanocytes
(1 for every 36 keratinocytes) can be identified by their pale (empty)
cytoplasm and dark nuclei among the keratinocytes of the stratum basalis. These cells do not contain tough keratin
filaments and also shrink during tissue preparation.
A
basement membrane exists between the
epidermis and dermis. Reticular fibers
are present in the basement membrane and account for the prominence of this structure
after PAS staining. Note that the
border between the epidermis and dermis known as the dermal-epidermal junction is irregular because numerous upward
interdigitations known as dermal
papillae indent the undersurface of the epidermis. Papillae are far more prominent in thick
skin than in thin skin since they serve to help these surfaces resist shear
forces and friction. Rete pegs are corresponding elongated
downward projecting ridges of epidermis.
Some rete pegs are narrower than others are and they are the ones, which
receive the sweat ducts. Under oil immersion, note that the basal
cells of the larger pegs have very fine processes, which anchor the cells to
the basement membrane. Basal cells of
the narrow ridges are smoother, allowing them to shift more easily.
Study slide A99,
thick skin, foot, monkey, (H&E), or slide BB-41, thick skin,
monkey, (H&E). Look at the dense
irregular connective tissue known as the dermis. Note that it is somewhat
subdivided into an upper thin papillary
layer and a thicker, deeply position reticular
layer. The papillary dermis will stain lighter because the collagen fibrils
are not as large or as extensively cross-linked or packed. This facilitates
diffusion of molecules that nourish the overlying a vascular epidermis.
Numerous capillaries are present in
the papillae of the papillary layer. Meissner's
corpuscles (encapsulated sensory nerve endings for touch that resemble
sectioned pinecones) can be seen in some papillae (see Figure 57 below). The
reticular layer of the dermis is so named because of the woven arrangement of
the heavily cross-linked collagenous fibers (in the form of a close meshed net)
and not because of the presence of reticular fibers. Note that the collagenous
fibers, although cut in transverse, oblique, and longitudinal planes, run
parallel and not vertical to the epidermis.
Figure 57: Micrograph of a
Meissner’s corpuscle in a dermal papillae.
Taken from Wheater’s Functional Histology, a text and colour atlas,
p. 141, Figure 7.28a.
The dermis is
similarly arranged in thin skin and can be viewed in slides A95-A98.
Identify blood vessels, nerve fascicles, and ducts of sweat glands in the reticular dermis. Secretory portions of
eccrine sweat glands can be seen
deep in the reticular dermis and extending deeper into the upper hypodermis. In
addition to the secretory portions of sweat glands, the hypodermis
(subcutaneous connective tissue) contains lobules
of adipose tissue, which are separated by strands of collagenous
fibers. When these septae become
excessively filled with well-nourished adipocytes,
the surface of the skin becomes dimpled and the appearance is known as
cellulite.
Study slide A95,
scalp, human fetus, (H&E), slide A96, non-specified thin
skin, (H&E), slide A97, pigmented and non pigmented skin,
(H&E), and slide A98, axillary skin, human, (H&E).
Compare the epidermis of thin skin with that of thick skin (A99). Note that the epidermis of thin skin has far
fewer cells in each of its layers (i.e., the total thickness of the stratum
corneum, stratum granulosum, and stratum spinosum are greatly reduced in
thickness). Identify the melanocytes with dark nuclei and pale
cytoplasm that can be seen interspersed between the keratinocytes in the
stratum basale. Note that the brown
melanin pigment that is present in Slides A96 and A97 is confined
to the keratinocytes in either the basal epidermis or those in the hair
bulb. A few pigment containing
macrophages can occasionally be seen in the dermis. These cells are phagocytic
and do not produce pigment. Note that
the dermal papillae and rete pegs are less developed than in
thick skin thus the waviness of the dermal-epidermal junction is not as
pronounced. The dermis is comparable to
that of thick skin in that it has a thinner, more superficial papillary layer
and a thicker, more deeply situated reticular layer.
Identify
the small blood vessels of the subpapillary
plexus. They are located at the
junction of the reticular layer and the papillary layer. Vessels arising from this plexus can be seen
as capillaries and arterioles in the dermal papillae. The papillary blood vessels are in close association with the
epidermal cells, which require nourishment for their growth and development.
Study slide A97,
skin, human, pigmented and non-pigmented, (H&E). This section shows melanin deposition in heavily pigmented (type
V or VI) epidermis. Melanin, the
pigment largely responsible for skin color, is produced by melanocytes, which
number about the same in all races but differ in the amount of melanin they
produce. Melanin is transferred via long cytoplasmic processes of melanocytes
to the intercellular spaces where it is taken up by keratinocytes and placed in
a supranuclear position melanosomes.
Cell bodies and cytoplasmic processes of melanocytes are not clearly
shown by conventional stains, but they can be demonstrated by treatment of
sections with dihydroxyphenylalanine (DOPA).
The DOPA reaction demonstrates that the cell bodies of most melanocytes are
located in the stratum basale while their cytoplasmic processes (some times
called dendritic processes) extend between cells of the stratum spinosum. Cells from the melanocytic lineage can also
be identified by immunostaining using an S-100 antisera.

Figure 58: Schematic diagram
of skin appendages. Taken from Wheater’s
Functional Histology, a text and colour atlas, p. 164, Figure 9.9.
Study slide A95,
scalp, human fetus, (H&E). Identify
the pigment containing cells in the epidermis and in the bulbs of hair follicles. Begin to recognize either cross sections or
longitudinal sections of hair follicles in the dermis and hypodermis. Identify sebaceous glands and arrector
pili muscles in the dermis. These
structures will be located at a mid-dermal region in association with hair
follicles. Together they are called the
pilosebaceous apparatus. Compare with
Figure 58 above.

Figure 59: Micrographs of
sebaceous glands. Left photo shows the
relationship between the arrector pili muscle (M) to the hair follicle (F) and
sebaceous gland (G). Right photo is a
higher magnification of the sebaceous gland.
Taken from Wheater’s Functional Histology, a text and colour atlas,
p. 168, Figure 9.14a & c.
Study slide A96. This section also has abundant sebaceous
glands. See Figure 59 above. Study keratinocytes found in sebaceous
glands and note the fine vacuoles of lipid in all but the most peripheral cells
(those resting on the basement membrane).
The small, cuboidal cells -bordering the basement membrane undergo
mitosis to replenish the more central ones which accumulate lipid and are lost
as the glandular secretion. As a cell
accumulates fat droplets, it enlarges to become polyhedral or spherical in
shape. The nucleus becomes pyknotic and
the entire cell eventually disintegrates to enter the sebaceous gland duct as sebum.
This mode of secretion in which the entire cell is lost is called holocrine secretion, and is
characteristic of sebaceous glands. Find a duct,
which connects with the alveoli of a sebaceous gland. Ducts are lined with stratified squamous epithelium and open into
hair follicles. Sebaceous glands in
some locations (e.g., those in the margins of the lips, nipple, and glans and
prepuce of penis) do not connect with hair follicles, but directly onto the
surface of the skin.
From
your visualization of sebaceous glands, attempt to relate their structure and
function. What type of secretion do
they produce and what effect does it have on the skin? Recalling the skin
problems of adolescence, remember that hormones influence sebaceous
glands? What might result from blockage
of the duct or hair follicles into which a sebaceous gland secretes?
There
are two classes of sweat glands
(sudoriparous glands), merocrine and
apocrine. Most sweat glands of the body are of the merocrine type and are
usually referred to as eccrine sweat
glands. They are most numerous in
the skin of the palms, soles, and forehead.
It has been estimated that they number about 3000 per square inch in the
palm of the hand. They are called
merocrine glands because they secrete by the merocrine method, i.e., no part of the cell is lost with the
secretion. Secretion leaves the cells
in a manner that might be described as reverse
pinocytosis. Apocrine sweat glands
are encountered in only a few areas, e.g., in the axillae and in the anogenital
region. They are called apocrine glands
because they secrete by the apocrine method, i.e., the apical portion of the
cell breaks off to form part of the secretion.
Both types of sweat glands are simple
coiled tubular glands. This means
that each sweat gland has its own duct (one duct per gland) and that the
secretory portion of the gland is a small-coiled tube.
Examine eccrine sweat glands in slides
A95, A98, A99 or BB-41, (H&E).
Secretory portions of the glands lie deep in the dermis, at the
dermal-hypodermal junction, or occasionally within the hypodermis. A section through the secretory portion of a
sweat gland will cut the coiled tubule into several cross sections (see Figure
60 below, left photo). It may appear
that two layers of secretory cells line a tubule, but the outermost cells with
somewhat elongated nuclei are the myoepithelial
cells, which occupy a
constant position between the basement membrane and the base of the secretory
cells (see Figure 60 below, right photo).
Myoepithelial cells have long contractile processes, which embrace the
secretory cells and squeeze out the secretion.
The processes are not visible in H&E preparation, but they can be
demonstrated by the alkaline phosphatase technique. Myoepithelial cells are
also present in other glands, salivary glands, and mammary glands, and in each
instance they occupy a similar position between the basement membrane and the base
of the glandular epithelial cell. In
addition to basally located myoepithelial cells, pale cuboidal secretory cells can be seen surrounding the lumen of the
secretory tubule.

Figure 60: Micrographs of
eccrine sweat glands. Left photo shows
the secretory portion (S) of the gland with its accompanying excretory duct
(D). Right photo is a higher
magnification of the left photo.
Myoepithelial cells (M) are shown between the epithelial cells and the
basement membrane. Taken from Wheater’s
Functional Histology, a text and atlas, p. 169, Figure 9.15.
Intradermal sweat ducts are lined by two layers of cells whose cytoplasm is darker
than that of secretory cells. The
two-layered epithelium of the sweat duct is classified as stratified
cuboidal. Myoepithelial cells are
absent in the duct.
Study slide A99
or BB-41. Identify the ducts,
and, if possible, find one as it enters a rete peg to become an intraepidermal sweat duct. Cells of the intraepidermal duct contain
keratohyalin granules and become keratinized near the stratum corneum.
Study slide A98,
axillary skin, human (H&E).
Identify the apocrine glands and compare with the eccrine glands in the
same section. Secretory portions of
apocrine glands are much larger than secretory portions of eccrine glands and
their lumina measure as much as 200 μm in diameter (see Figure 61 below).
This is ten times the average diameter of lumina of eccrine sweat glands. Apices of some cells of apocrine glands are
rounded and can be seen breaking off to enter the lumina as part of the
secretion. This mode of secretion where
part of the cell is lost is termed apocrine
secretion. Myoepithelial cells are present in secretory portions
of apocrine glands, and appear even more prominent than in eccrine glands.

Figure 61: Micrograph of
apocrine sweat glands. Taken from Wheater’s
Functional Histology, a text and colour atlas, p. 170, Figure 9.16.
The
intradermal ducts of apocrine glands
have the same histological appearance as corresponding ducts of eccrine glands. They are devoid of myoepithelium and have a
double layer of dark staining epithelial cells, which have a periluminal cuticle. The latter becomes especially prominent as
the duct traverses the papillary layer of the dermis. Most ducts of apocrine glands open into hair follicles, but some
open directly onto the surface, as do all eccrine ducts. Quite commonly, more than one apocrine duct
empties into the same hair follicle, usually entering the follicle slightly
above the opening of the sebaceous duct.
Apocrine
and eccrine glands have other differences in addition to those of histological
importance. Eccrine glands are supplied
with cholinergic fibers while
apocrine glands are supplied with adrenergic
fibers. Eccrine glands serve
primarily in heat regulation whereas apocrine glands represent scent glands
similar to those producing pheromones in lower animals. Both types of glands are stimulated to
secrete by stresses such as fright and pain, but eccrine glands also respond to
heat while apocrine glands do not. In
contrast to eccrine glands, apocrine glands are greatly influenced by hormones,
becoming active about the time of puberty and showing secretory variation
during the menstrual cycle.
Hair Follicles/Nails
Study
hair follicles in various stages of the hair growth cycle on scalp (slide
A95) or axilla (slide A98). Keratinocytes that form these appendages grow downward from the
surface during the 3-4 month of development.
The stem cell population resides in the
bulge region where the erector pili
muscle inserts into the hair shaft.
Periodically these cells grow downward (anagen growth phase), form an expanded hair bulb in the deep dermis
or hypodermis and begin to undergo a special pattern of differentiation that
will produce a highly keratinized structure known as hair. The transiently amplifying hair matrix cells are found at the
upper indentation of the hair bulb above of a tuft of capillaries, the dermal hair papilla that provide
nourishment. Melanocytes also populate
the hair bulb region and provide coloration to the hair. The cells lining the outer surface of the
length of the hair follicle are known as outer
root sheath cells and the multiple inner cell layers are known as inner root sheath cells.
Hairs (terminally differentiated cells that are equivalent
to dead stratum corneum
squames on the
surface) move upward where they become coated with sebum (oil) and eventually
erupt at the epidermal surface. Hair
(totally dead cells) has an outer cuticle
and an inner cortex. Periodically the hair bulb begins to regress
upward to the bulge region (catagen
phase), the hair is shed at the surface, and the hair follicle enters the telogen (resting) phase. The length of the hair growth cycle and the
type of hair (terminal hair on the head, vellus-fine hair, pubic hair) is
determined by local signals as well as hormones.
Fingernails
and toe nails represent yet another type of differentiation (see Figure 62
below). The nail matrix cells are
located under the skin fold at the proximal region of the distal phalanx (see
fetal finger on Slide A34).
Destruction of nail matrix cells will result in a permanent nail
loss. The more differentiated cells
advance toward the fingertip. The newly
differentiated cells form a crescent-shaped lunula (white region that is
grossly visible). The proximal dead
skin that is carried forward by continuous nail growth is known as the eponychium and the fold of skin
underneath the distal growing tip is called the hyponychium. The dead nail
advances across epidermal cells called the nail
bed.

Study
the section of thick skin on Slide A99 or BB-41 and look for a glomus body. If one is not present on your slide, study a glomus body in the
textbook or atlas. The glomus body is
an arterio-venous anastomosis
located in the dermis surrounded by a capsule of connective tissue. Several sections of arteries and veins
appear within the capsule and the sections of arteries show much smooth muscle
in their walls. Glomus bodies are most
numerous in the dermis of the fingers and toes and play a role in temperature
regulation. Upon exposure to cold
temperatures, a decrease in papillary blood flow shunts blood away from the
surface resulting in conservation of body heat at the expense of digital
circulation and possible frostbite.