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Zorina, A.;  Zorin, V.;  Kudlay, D.;  Kopnin, P. Changes in Homeostasis of the Dermal Extracellular Matrix. Encyclopedia. Available online: (accessed on 28 February 2024).
Zorina A,  Zorin V,  Kudlay D,  Kopnin P. Changes in Homeostasis of the Dermal Extracellular Matrix. Encyclopedia. Available at: Accessed February 28, 2024.
Zorina, Alla, Vadim Zorin, Dmitry Kudlay, Pavel Kopnin. "Changes in Homeostasis of the Dermal Extracellular Matrix" Encyclopedia, (accessed February 28, 2024).
Zorina, A.,  Zorin, V.,  Kudlay, D., & Kopnin, P. (2022, June 20). Changes in Homeostasis of the Dermal Extracellular Matrix. In Encyclopedia.
Zorina, Alla, et al. "Changes in Homeostasis of the Dermal Extracellular Matrix." Encyclopedia. Web. 20 June, 2022.
Changes in Homeostasis of the Dermal Extracellular Matrix

Skin aging is a multi-factorial process that affects nearly every aspect of skin biology and function. With age, an impairment of structures, quality characteristics, and functions of the dermal extracellular matrix (ECM) occurs in the skin, which leads to disrupted functioning of dermal fibroblasts (DFs), the main cells supporting morphofunctional organization of the skin. The DF functioning directly depends on the state of the surrounding collagen matrix (CM). The intact collagen matrix ensures proper adhesion and mechanical tension in DFs, which allows these cells to maintain collagen homeostasis while ECM correctly regulates cellular processes. When the integrity of CM is destroyed, mechanotransduction is disrupted, which is accompanied by impairment of DF functioning and destruction of collagen homeostasis, thereby contributing to the progression of aging processes in skin tissues. 

skin extracellular matrix collagen aging fibroblasts

1. Aging of Human Skin

Skin aging is a complex multifactorial process that develops throughout ontogenesis and affects all biological aspects of this human organ, a process that is determined by both internal factors (endogenous, genetic, and epigenetic) and external factors (exogenous). Among the external factors, ultraviolet irradiation (UV) plays a special role [1][2][3][4][5][6][7]. Thus, there are two types of skin aging: chronological (internal) and photoaging (external). Each type of skin aging has its own clinical and morphological features. The characteristic signs of chronological aging are skin thinning, dryness, decreased elasticity and firmness, paleness, and the presence of fine surface wrinkles. Photoaging occurs under chronic UV exposure; in particular, long-wavelength UVA of 320–400 nm [7] can be observed even before the manifestations of chronological aging. Photoaging results in skin thickening, coarsening, dehydration, deep wrinkles, telangiectasias, irregular pigmentation, and solar lentigo [8][9].
Unlike chronological skin aging which is the genetically determined process depending on a person′s age, photoaging directly depends on the degree of UV exposure, is genetically predetermined by a degree of skin pigmentation [10][11][12], and is considered as an accelerated process of chronological aging [4][13]. The skin in the exposed body areas (face, neck, and hands) undergoes the impact of solar radiation and other environmental factors that cause destructive processes which are believed to be superimposed on chronological skin aging and thereby accelerate its development [14].
Both internal and external aging is primarily associated with phenotypic changes in cells, while the functional manifestations of skin aging are caused by structural and compositional remodeling of the main structural proteins of the extracellular matrix (ECM) in the skin [10].
Skin involution is based on processes occurring at the molecular level which destroy the integrity and structural organization of the genetic material, lead to modification and aggregation of intracellular and extracellular proteins, damage membranes, and cause mitochondrial dysfunction [15]. These processes are accompanied by the decrease in biosynthetic cellular activity, the reduction in the number of active progenitor cells, and the change in molecular composition of ECM. The latter, in turn, is caused by impaired gene expression and post-translational modifications which are mainly distinct in fibrillar proteins. The imbalance occurs between ECM synthesis and decay, which leads to the decrease in tissue mass, the accumulation of degraded molecules in the ECM, and lowering of the functional efficiency of all skin components [5][16].
Aging of each of the skin layers is characterized by its own specific features, which is clinically manifested by thinning of the epidermis, flattening and weakening of the dermo-epidermal junction (DEJ), and the decrease in thickness of the dermis and the hypodermis (Figure 1) [3][17][18][19][20].
Figure 1. Schematic representation of skin aging.

2. Aging of the Epidermis and the Dermo-Epidermal Junction

Thinning of the epidermis (by 10–50% between the ages of 30 and 80) occurs mainly due to migration of basal keratinocytes (BKs) which have lost their proliferative potential into the spinous layer [21][22][23]. The BK cell population is characterized by the decrease in cell proliferation, quantity, and ability to self-renew. This leads to impairment of epidermal morphogenesis, the decrease in the rate of tissue renewal, and its thinning [24][25][26][27]. Histological examination of skin biopsy samples of elderly people confirms distinct changes in the basal layer of the epidermis, including significant heterogeneity in the size of keratinocytes [28].
One of the main factors contributing to disruption of homeostasis in the BK population is the decreased level of type XVII collagen (COL17), a transmembrane protein of hemidesmosomes which through to attach keratinocytes to the basement membrane (BM) [29]. Apparently, this protein plays a key role in the proliferation of BKs [30]. It has been shown that the resulting differential expression of the COL17A1 gene in BKs promotes competition among these cells, whereas the protein loss contributes to impairment of homeostasis in the BK pool followed by its depletion, which inevitably leads to the degradation of hemidesmosomes and disruption of epidermal morphogenesis [29].
With age, changes also occur in the population of melanocytes: their functional activity reduces, their number decreases (by 20% every 10 years), and their heterogeneity increases. As a result, uneven skin pigmentation appears [2][26][31][32][33]. There is also a decrease in the activity and number of Langerhans cells (antigen-presenting cells), which causes a decrease in the immune functions of the skin [10][31][34]. As we age, not only a thinning of the epidermis occurs. The production of epidermal lipids is impaired, while the significant decrease in their amount leads to the development of dry skin despite the fact that thickness of the stratum corneum and its hydration remains virtually unchanged [35]. Dryness of the skin is also promoted by the decreased level of hyaluronic acid (HA) in the epidermis and the glycosaminoglycans (GAGs) which have the largest molecular weight and facilitate water binding and tissue hydration (Table 1) [36][37][38].
Table 1. Changes in glycosaminoglycans and proteoglycans in the skin with age.
  Chronological Aging Photoaging
HA in theepidermis ↓ amount ↓ amount
HA in the derma amount not changed
↓ bioavailability
↑ amount
↓ length
Total content of sulphated GAGs ↓ amount ↑ amount
Versican ↓ mRNA expression
↑ amount in males
↓ mRNA expression
↑ amount in the solar elastosis area
Decorin ↓ mRNA expression
↓ amount
↓ size
↓ amount in the solar elastosis area
Biglycan ↓ mRNA expression
↓ amount
↓ amount
Age-related destructive changes also occur in the underlying dermal structures, in the dermo-epidermal junction (DEJ) (Figure 1), such as a flattening and reduction in the total surface area of DEJ; a smoothing of the epidermal ridges (due to a decrease in their number and size); a thinning of BM and its multilayering (which apparently has a compensatory character due to flattening of the epidermal ridges [39], while a decrease in the amount of type IV collagen begins after 35 years [40]); as well as the disorganization and degradation of anchoring fibrils [18][19][20].
According to A. Langton (2016), the significant decrease occurs in the level of DEJ main proteins, namely, collagens (types IV, VII, and XVII), integrin β4, and laminin-332, which leads to disturbance of the structural integrity of DEJs and weakens the connection between the epidermis and the dermis [20]. The latter, in turn, causes disruption of metabolic processes between these skin layers and, thus, reduces the supply of nutrients and signaling cytokines to the epidermis, which has a negative effect on the proliferation of BKs by disrupting the homeostasis of their population [21][41][42]. At the same time, the epidermis is also influenced by the state of the dermis, i.e., the water content in “the ground substance” (integrative buffer gel) and the integrity of the collagen–elastin matrix [43].

3. Aging of the Dermis

According to the results of histological and ultrastructural studies, the dermis is the skin layer focusing the most significant changes associated with skin aging [13][44]. This occurs primarily due to structural changes in dermal ECM, its reduction, and degradation [2].
The fibers (collagen and elastin) that constitute the skin framework and are the components of “the ground substance”, as well as proteoglycans (PG) and GAGs which play a key role in maintaining firmness and hydration of the skin, undergo particularly prominent degenerative changes [4][10]. As a result of these processes, firmness and elasticity of the skin is lost, its thickness decreases, and wrinkles form [18][34][40][41].
The changes affect both layers of the dermis; the papillary is the upper and thinner layer, while the reticular is the next more pronounced layer [4][10][42][45]. In the papillary layer that is adjacent to BM, a decrease in the content of perlecan (the main PG of BM) and GAG hyaluronic acid is detected (echographically visualized as a subepidermal anechogenic zone [46]), as well as a decrease in the density and spatial orientation of collagen fibers [47][48][49]. In the elastin network of the papillary layer of the dermis, the progressive atrophy of oxytalan fibers is observed, up to their complete disappearance [10][50].
In the reticular layer, a decrease in the density of collagen fibers is accompanied by a decrease in the thickness of their bundles and an increase in the space between them [51], while the thickening of fibers (elaunin and elastin) and a decrease in the number of functional fibers is observed in the elastic network [10][50].
Under the chronic UVA exposure, solar elastosis affects the elastin network of both dermal layers, i.e., there is the deposition and accumulation of elastin masses possessing the incomplete molecular organization and, therefore, the incomplete function. This phenomenon is explained by the stimulating effect of UV on the expression of the gene responsible for the synthesis of elastin. Solar elastosis zones are also characterized by the accumulation of PGs [5][10].
It should be emphasized that changes in the organization and structure of the collagen matrix are characteristic of both chrono- and photoaging of human skin [2]. The results of the study of skin biopsy samples of elderly people have shown that the accumulation of degraded/fragmented fibers and a decrease in de novo collagen synthesis correlate both with age and with the degree of photo-damage severity [51][52][53][54].
Along with degradation of the collagen–elastin matrix, changes also occur in “the ground substance” of the dermis, which is associated with the quantitative and qualitative transformation of GAGs and PGs (Table 1) responsible for hydration and elasticity of the skin. In particular, the bioavailability of HA decreases significantly with age (although its amount remains unchanged [34]), as well as biglycan [36].
Proteoglycan decorin, that is, the smallest in size and the most important regulator of the assembly of collagen fibers, also undergoes quantitative and qualitative changes, while a decrease in the molecular weight of its polysaccharide chains has a significant negative effect on skin elasticity since decorin is involved in fibrillogenesis and determines the diameter of fibrils [36][55]. It has been shown that during photoaging, the abnormal accumulation of HA, versican, and chondroitin sulfate is observed in the solar elastosis zones, while decorin is completely lost; all these phenomena are caused by chronic damage of the skin under UV exposure [36].
Histological examination of skin biopsy samples of young and elderly people confirms the changes described above. Thus, the histological picture of skin sections [4] showed that the “young” and photoprotected skin is characterized by the pronounced epidermal ridges and DEJs, as well as the highly organized network of collagen fibers and a cascade of elastic network fibers connecting BM with the papillary and reticular layers of the dermis; while the chronologically aged skin is characterized by the reduced collagen fibers and elastic network fibers (especially oxytalan fibers) and the reduced content of GAGs, whereas the photoaged skin is characterized by the reduction in collagen fibers, including type VII collagen in the area of DEJs, and by solar elastosis, that is, the accumulation of disorganized proteins of elastin fibers throughout the dermis and also the accumulation of GAGs. In the case of chronological aging of the photoprotected skin, the flattening of DEJs is observed, as well as the disorganization of the elastic network (mostly in the papillary layer), which is accompanied by the accumulation of amorphous elastin and a reduction in the number of collagen fibers. During photoaging, the skin of both young and elderly patients is characterized by the pronounced destruction of epidermal ridges and DEJs, degradation of the elastic network, and accumulation of amorphous elastin in both layers of the dermis. Aging and UV exposure cause the disorders observed in the integrative buffer system of the dermis, a decrease in functioning of the highly organized network of elastic fibers connecting all layers of the skin through cascading, and structural deformations of collagen fibers including their progressive fragmentation. All these events change the essential functional properties of the skin by reducing the skin hydration, elasticity, firmness, and strength [2][4][46][54]. As regards the collagen fragmentation, it is important to note the degradation of type I collagen fibers, the most common structural fiber-forming protein of the skin, which comprises 80–90% of the total collagen amount, while the other two fiber-forming collagens type III collagen and type V collagen are 8 to 12% and up to 5%, respectively [44]. With age, the level of total collagen in the skin decreases (by approximately 1% throughout the entire adult person’s life [56]), and the level of main collagen types I and III also decreases, especially at the age of over 60 [57]. According to other data, the increase in collagen type III/I ratio occurs with age due to the increased degradation of type I collagen [58].

4. The Relationship between the State of Collagen Matrix and Functioning of Dermal Fibroblasts

It has been shown that signals entering the dermis from outside are perceived by the ECM and transmitted to DFs, which, receiving these signals, provide ECM homeostasis [13][51][59]. At the same time, the DF functioning directly depends on the state of the surrounding collagen matrix (CM). The intact CM ensures proper adhesion and mechanical tension in DFs, which allows these cells to provide collagen homeostasis while the ECM fully regulates cellular processes including cell migration, proliferation, differentiation, and apoptosis [60].
When the CM integrity is damaged, which occurs both during chronological aging and photoaging, changes are observed in mechanotransduction (transmission of mechanical signals from ECM to cells), promoting development of the mechanism that disrupts DF functions (Figure 2) [13][53][61][62].
Figure 2. Schematic representation of the relationship between mechanical tension of CM and the DF cytoskeleton during collagen production in the human dermis.
It has been revealed that integrins (heterodimeric transmembrane proteins, specific receptors, primarily, α1β1 and α2β1 to collagen type I [63]) located on the cell surface are able to specifically bind ECM proteins, in particular type I collagen [53]. The adhesion of integrins to ECM proteins contributes to the formation of bonds not only between integrins and the collagen matrix but also with actin (protein of the DF cytoskeleton) since integrins are attached to the CM from the outer surface of the cell membrane and connected to the cytoskeleton from the inner surface of the cell membrane, thereby creating focal adhesion complexes (focal contacts) that ensure the closely related regulatory and mechanical functions of DFs [11][53][64]. The formation of these complexes induces a cascade of intracellular signaling pathways that regulate the DF metabolism including the balance between production of collagens and their degradation by MMPs. Due to the focal contacts, DFs can “spread out” on the CM, which allows intracellular microfilaments to exert mechanical pressure on the matrix. At the same time, the cytoskeleton microfilaments located on the inner surface of the cell membrane and in the cytoplasm are physically linked to integrins and use this coupling to tighten the collagen network [13]. The internal tension of actin–myosin microfilaments (AMF) activates the complex of intracellular microtubules and intermediate filaments, contributing to the formation of pressure from the outside. A balance is created between the external pressure and the internal tension of AMF, which results in a dynamic tension between DFs and CM. This allows DFs to achieve the proper level of stretching which ensures the possibility of perfect functioning, including the synthesis of collagen and other ECM components [63]. When the structural integrity of CM is disrupted, the mechanical tension decreases which leads to the reduction in DF focal adhesion and violates the mechanical resistance of collagen fibers. As a result, the balance between the tension inside DFs and the pressure outside them is disturbed. For this reason, DFs lose their ability to stretch and, therefore, reduce the production of collagen, while the production of MMPs, on the contrary, increases, contributing to even greater disorganization of collagen fibers. Thus, the production of collagen in the elderly (80 years and older) compared with its synthesis in the skin of the young (18–29 years) decreases by about 75% [11][53], while the level of collagen degradation (similar to photoaging) increases by 75% [11]. Moreover, there is a parallel decrease in the content of collagens of types I and III, which constitute the main structural fibers of the dermal ECM [65][66].
Despite the different etiologies, the disorders observed in both types of aging are based on the common fundamental molecular mechanisms. The oxidative stress is believed to be the main trigger of these destructive processes [65][67].


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