In more than 100 years of research and development, Shiseido has continued to face the eternal skin concerns of consumers, including sagging, wrinkles, spots, and dullness, while evolving the observation technology and worked towards the elucidation of contributing factors and development of solutions. In recent years, we focused on the conditions inside the skin, including blood vessels, lymph ducts, immunity, and nerves, and deepened the research in the relationship of these structures and the skin conditions.
Shiseido has repeatedly elucidated findings regarding the age-related changes in facial contour, sagging, as a pioneer in this research area.
The results are evaluated highly in international research forums hosted by IFSCC*, including the receipt of conference awards four times in succession.
We elucidated the cause of sagging for the aged appearance and discovered the Dynamic Belt, which is a system where the skin resists the deformation caused by gravity. The Dynamic Belt is a mechanism where the hair muscles on the face at high density resists gravity.
We have closed in on the root cause of wrinkles and deepened the research on solution as pure retinol as the only retino-related substance in Japan with the indication of wrinkle improvement as Shiseido's representative technology in improving wrinkles.
Using the independently developed cutting-edge technology for imaging skin elasticity in three dimensions, we analyzed the mechano-physical properties of skin for consumers in various age groups, from young to senior, and found that the “balance of elasticity between the stratum corneum and the dermis” deteriorates with age, concluding that such phenomenon is the root cause of wrinkle formation.
We closed in on the mechanisms of pigmentation and dullness and have worked to develop solution materials ranging from the independently developed brightening active ingredient potassium 4-methoxysalicylate and tranexamic acid to a variety of plant extracts.
We have elucidated part of the mechanism by which photoaging*1 and other factors induce acquired genetics (epigenetics) to make skin dull.
We develop technology for non-invasive observation of the conditions of blood vessels, lymph ducts, immunity, and nerves that exists in the skin and play a role in linking the skin to the entire body, while also elucidating the relationship with the beauty of the skin.
We discovered for that Fermented Camellia Seed Extract can increase the expression of CXCL9, which potentially recruits the immune cells CD4 CTL(Memory T cells) having the function to eliminate senescent fibroblasts in the skin. In other words, Fermented Camellia Seed Extract is expected to enhance the effect of skin immune cells to eliminate senescent cells.
We discovered as a new function of skin’s immune cells the elimination of aged fibroblasts (senescent cells) and its mechanism. Advancing age alone does not correlate with the accumulation of senescent cells in the human skin. Among the potential mechanisms, Cytotoxic CD4+ T cell (CD4 CTL) , a type of immune cells, are strongly associated with the inhibition of accumulation of senescent cells.
We gained understanding of the mechanism in which capillaries contribute to skin elasticity, and identified that neem leaf extract and Houttuynia cordata extract work effectively for maintaining thick (large diameter) and stable capillaries, which can become thinner and regress due to aging and ultraviolet rays, etc.
We have elucidated the aging mechanism of lymphatic vessels in the skin for the first in the world by applying its unique skin visualization technology*1.
Our new discovery revealed that the downregulation of IL-34 (interleukin 34), a protein secreted in the epidermis, skews the M1/M2 balance, a balance between two types of macrophages (M1 macrophages and M2 macrophages), which has previously been found to be involved in skin aging and collagen metabolism.
We revealed that the balance between two types of macrophages*1 (the M1/M2 balance) is involved in a series of collagen metabolism, collagen production, fragmentation, and degradation in photoaged skin.
We found that the number of Langerhans*2 precursor cells*3 (hereafter, LC precursor cells) is reduced in the dermis of aged skin, and that decreased expression of CXCL14 that recruits LC precursor cells to the epidermis might result in the reduction of mature epidermal Langerhans cells.
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