HaCaT cells are the immortalized human keratinocytes and have been extensively used to study the epidermal homeostasis and its pathophysiology. T helper cells play a role in various chronic dermatological conditions and they can affect skin barrier homeostasis. To evaluate whether HaCaT cells can be used as a model cell system to study abnormal skin barrier development in various dermatologic diseases, we analyzed the gene expression profile of epidermal differentiation markers of HaCaT cells in response to major T helper (Th) cell cytokines, such as IFNγ, IL-4, IL-17A and IL-22. The gene transcriptional profile of cornified envelope-associated proteins, such as filaggrin, loricrin, involucrin and keratin 10 (KRT10), in HaCaT cells was generally different from that in normal human keratinocytes (NHKs).
HaCaT cells are the immortalized human keratinocytes and have been extensively used to study the epidermal homeostasis and its pathophysiology. T helper cells play a role in various chronic dermatological conditions and they can affect skin barrier homeostasis. To evaluate whether HaCaT cells can be used as a model cell system to study abnormal skin barrier development in various dermatologic diseases, we analyzed the gene expression profile of epidermal differentiation markers of HaCaT cells in response to major T helper (Th) cell cytokines, such as IFNγ, IL-4, IL-17A and IL-22. The gene transcriptional profile of cornified envelope-associated proteins, such as filaggrin, loricrin, involucrin and keratin 10 (KRT10), in HaCaT cells was generally different from that in normal human keratinocytes (NHKs).
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HaCaT cells are immortalized human keratinocytes, which have been widely used to study epidermal homeostasis and its pathophysiology. T helper cells play a role in various chronic skin diseases and can affect the balance of skin barrier in vivo. In order to evaluate whether HaCaT cells can be used as a model cell system to study the development of abnormal skin barrier in various skin diseases, we analyzed the gene expression profiles of the epidermal differentiation markers of HaCaT cells in response to major T helper (Th) cytokines, su as IFNγ, IL-4, IL-17A and IL-22. The gene transcription profiles of corneal associated protein, such as filaggrin, loricrin, inclusion protein and keratin 10(KRT10) in HaCaT cells are basically different from those in normal human keratinocytes (NHKs).
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