Extended skin tissue samples
The Tissue atlas is based on immunohistochemical staining of tissue microarrays from 44 different normal tissue types. In addition to the standard setup, extended tissue profiling is performed for selected proteins, to give additional data about where the protein is expressed. Extended tissue samples include mouse brain, human lactating breast, eye, and additional samples of adrenal gland, skin and brain. For extended skin samples, both tissue sections and tissue microarrays with 2 mm diameter samples are used for further exploration of proteins expressed in hair, hair follicles, sweat glands and sebaceous glands.
Hair and hair follicles
Hair is found almost everywhere on the body and arises from hair follicles, which are epidermal derivatives present in the connective tissue layer of skin, called dermis. The duration of hair growth (anagen), growth arrest (catagen) and resting periods (telogen) is different throughout the body. Specifically, the growth of hair on the scalp and face is highly influenced by sex hormones, mainly androgens.
The hair can be divided into three layers, namely the medulla, cortex and cuticle layer, all originating from cells at the base of the hair bulb, the dermal papilla. The medulla consists of moderately keratinized cells, while the cortex is formed by compact, heavily keratinized cells, and the surrounding cuticle layer forms a protective layer for the hair shaft. Melanocytes, which are responsible for hair pigmentation, are present in the dermal papilla.
The hair follicle is an epidermal invagination that encloses the initial part of the hair shaft. The hair follicle is composed of two distinct layers: the internal and external root sheath. One example of a protein expressed in the hair follicle is the type II cytoskeletal keratin 71 (KRT71). KRT71 is specifically expressed in the internal root sheath, where it plays a significant role in the formation of hair (Figure 1).
The full list of proteins analyzed in hair and hair follicle samples is found in Table 1.
Figure 1. Immunohistochemical staining of human hair follicles using an antibody toward KRT71 shows strong cytoplasmic staining in the internal root sheath.
Table 1. The following 32 genes have been analyzed for expression in hair and hair follicles using extended skin tissue samples.
Sweat glands
Sweat glands are tubular structures in the skin and can be separated into two main types: eccrine sweat glands and apocrine sweat glands. These are different in structure, function, secretory product, mechanism of excretion and distribution in the skin. The eccrine glands can be found throughout the body in varying densities, especially in thick skin, and are primarily involved in the cooling of the human body. The secretory unit is located in the dermis layer and consists of a coiled base that discharges a water-based secretion through a duct, which empties on the surface of the skin. An example of a protein expressed in eccrine sweat glands is dermcidin (DCD), previously known as an antimicrobial peptide important for the innate immune system (Figure 2). Apocrine sweat glands are located to certain parts of the body e.g. armpits, ear canals and eyelids. These glands have also a coiled tubular structure, but empty an oily secretion into hair follicles.
Extended tissue profiling is only assessed in eccrine sweat glands.
Figure 2. Immunohistochemical staining of human skin using an antibody toward DCD shows strong membranous and cytoplasmic positivity in sweat duct cells and secretory cells.
Sebaceous glands
The sebaceous glands are located in the upper part of dermis. Similarly to apocrine sweat glands, they produce an oily or waxy secretion called sebum. One function is to lubricate and protect the hair and skin from water and thus acts as a protective barrier. This barrier function also results in reduction of water loss from skin surface. An example of a protein expressed in sebaceous glands is the elongation of very long chain fatty acids protein 3 (ELOVL3), which plays a role in elongation of long chain fatty acids (Figure 3). The full list of proteins analyzed in sebaceous and sweat gland samples is found in Table 2.
Figure 3. Immunohistochemical staining of human skin using an antibody toward ELOVL3 shows strong cytoplasmic positivity in cells in sebaceous gland.
Table 2. The following 6 genes have been analyzed for expression in sebaceous and sweat glands using extended skin tissue samples.
Relevant links and publications
Uhlén M et al, 2015. Tissue-based map of the human proteome. Science
PubMed: 25613900 DOI: 10.1126/science.1260419 Yu NY et al, 2015. Complementing tissue characterization by integrating transcriptome profiling from the Human Protein Atlas and from the FANTOM5 consortium. Nucleic Acids Res.
PubMed: 26117540 DOI: 10.1093/nar/gkv608 Fagerberg L et al, 2014. Analysis of the human tissue-specific expression by genome-wide integration of transcriptomics and antibody-based proteomics. Mol Cell Proteomics.
PubMed: 24309898 DOI: 10.1074/mcp.M113.035600 |
