Skip to Main Content

Login to your account

Show
Forgot password?
Don’t have an account?
Create a Free Account

If you don't remember your password, you can reset it by entering your email address and clicking the Reset Password button. You will then receive an email that contains a secure link for resetting your password

If the address matches a valid account an email will be sent to __email__ with instructions for resetting your password

Cancel
ADVERTISEMENT
SCROLL TO CONTINUE WITH CONTENT



Property Value
Status
Version
Ad File
Disable Ads Flag
Environment
Moat Init
Moat Ready
Contextual Ready
Contextual URL
Contextual Initial Segments
Contextual Used Segments
AdUnit
SubAdUnit
Custom Targeting
Ad Events
Invalid Ad Sizes
Advertisement
JID Innovations home
Close
  • Home
  • Articles & Issues
    • Back
    • Articles In Press
    • Current Issue
    • Issues in Progress
    • List of Issues
  • Collections
    • Back
    • Atopic Disease
    • Cancer
    • Cell Biology
    • Cover Gallery
    • Clinical & Translational Research
    • Genetic Disease
    • Immunity
    • Melanoma
    • New Methodology
    • Non-Melanoma Skin Cancer
    • Photobiology
    • Psoriasis
    • Training Physician Scientists
  • Authors/Reviewers
    • Back
    • Instructions for Authors
    • Submit a Manuscript 
    • Thank You, Reviewers
    • Contact
    • Permissions
  • Journal Info
    • Back
    • About the Journal
    • Contact the Editorial Office
    • Editorial Board
    • New Content Alerts
  • Advertisers 
  • SID
    • Back
    • SID Website 
    • Join SID 
    • Annual Meeting 
    • Academic Industry Partnership 
  • ESDR
    • Back
    • ESDR Website 
    • Join ESDR 
    • Awards 
    • Events 
    • Media 
    • Education 
  • Companion Titles
    • Back
    • Journal of Investigative Dermatology
    • Journal of Investigative Dermatology Symposium Proceedings
  • Contact
Advanced searchSave search

Please enter a term before submitting your search.

Ok
  • Submit
  • Log in
  • Register
  • Log in
    • Submit
    • Log in
Skip menu
    x

    Filter:

    Filters applied

    • Cell Biology

    Article Type

    • Research Article14
    • Review Article2

    Publication Date

    • Last 6 Months1
    • Last Year3
    • Last 2 Years14
    • Last 5 Years16
    Please choose a date range between 2021 and 2022.

    Author

    • Ara, Katsutoshi1
    • Avecilla, Alexa Regina Chua1
    • Bai, Wanzhu1
    • Barral, Duarte C1
    • Beck, Lisa A1
    • Bento-Lopes, Liliana1
    • Bergerat, David1
    • Brewer, Matthew G1
    • Budamakuntla, Leelavathy1
    • Cabaço, Luís C1
    • Carpenter, M Alexandra1
    • Castex-Rizzi, Nathalie1
    • Colley, Helen E1
    • Danby, Simon1
    • Davis, John M1
    • Ding, Chun-Lei1
    • Domenichiello, Anthony F1
    • Dubrac, Sandrine1
    • Eguchi, Ryoji1
    • Eichmann, Thomas O1
    • Evrard, Céline1
    • Faway, Emilie1
    • Ferreira, Andreia1
    • Flamion, Bruno1
    • Fontao, Fabienne1

    Journal

    • JID Innovations16

    Keyword

    • KC10
    • keratinocyte10
    • AD4
    • atopic dermatitis4
    • 3D3
    • knockout3
    • KO3
    • SC3
    • three-dimensional3
    • ECM2
    • FFA2
    • HDF2
    • HEE2
    • human epidermal equivalent2
    • LA2
    • TEER2
    • transepithelial electrical resistance2
    • 1,25(OH)2VD31
    • 1,25-dihydroxyvitamine D31
    • 13-hydroxy-9,10-epoxy octadecenoate1
    • 5-ethynyl-2'-deoxyuridine1
    • 9,10,13-THL1
    • 9,10,13-trihydroxy-octadecenoate1
    • 9,13-EHL1
    • ACD1

    Access Filter

    • Open Access

    Cell Biology

    16 Results
    Subscribe to collection
    • Export
      • PDF
      • Citation

    Please select at least one article in order to proceed.

    Ok
    FilterHide Filter
    • Original Article
      Open Access

      Endogenous Derivatives of Linoleic Acid and their Stable Analogs Are Potential Pain Mediators

      JID Innovations
      Vol. 3Issue 2100177Published online: December 25, 2022
      • Joshua J. Wheeler
      • Anthony F. Domenichiello
      • Jennifer R. Jensen
      • Gregory S. Keyes
      • Kristen M. Maiden
      • John M. Davis
      • and others
      Cited in Scopus: 0
      • Preview Hide Preview
      • Download PDF
      • Export Citation
        Psoriasis is characterized by intense pruritus, with a subset of individuals with psoriasis experiencing thermal hypersensitivity. However, the pathophysiology of thermal hypersensitivity in psoriasis and other skin conditions remains enigmatic. Linoleic acid is an omega-6 fatty acid that is concentrated in the skin, and oxidation of linoleic acid into metabolites with multiple hydroxyl and epoxide functional groups has been shown to play a role in skin barrier function. Previously, we identified several linoleic acid‒derived mediators that were more concentrated in psoriatic lesions, but the role of these lipids in psoriasis remains unknown.
        Endogenous Derivatives of Linoleic Acid and their Stable Analogs Are Potential Pain Mediators
      • Original Article
        Open Access

        Ninjurin1 Deletion in NG2-Positive Pericytes Prevents Microvessel Maturation and Delays Wound Healing

        JID Innovations
        Vol. 2Issue 6100141Published online: July 6, 2022
        • Risa Matsuo
        • Mari Kishibe
        • Kiwamu Horiuchi
        • Kohei Kano
        • Takamitsu Tatsukawa
        • Taiki Hayasaka
        • and others
        Cited in Scopus: 0
        • Preview Hide Preview
        • Download PDF
        • Export Citation
          The formation of mature vasculature through angiogenesis is essential for adequate wound healing, such that blood-borne cells, nutrients, and oxygen can be delivered to the remodeling skin area. Neovessel maturation is highly dependent on the coordinated functions of vascular endothelial cells and perivascular cells, namely pericytes (PCs). However, the underlying mechanism for vascular maturation has not been completely elucidated, and its role in wound healing remains unclear. In this study, we investigated the role of Ninjurin-1 (Ninj1), a new molecule mediating vascular maturation, in wound healing using an inducible PC-specific Ninj1 deletion mouse model.
          Ninjurin1 Deletion in NG2-Positive Pericytes Prevents Microvessel Maturation and Delays Wound Healing
        • Original Article
          Open Access

          RAB3A Regulates Melanin Exocytosis and Transfer Induced by Keratinocyte-Conditioned Medium

          JID Innovations
          Vol. 2Issue 5100139Published online: June 21, 2022
          • Luís C. Cabaço
          • Liliana Bento-Lopes
          • Matilde V. Neto
          • Andreia Ferreira
          • Wanja B.L. Staubli
          • José S. Ramalho
          • and others
          Cited in Scopus: 0
          • Preview Hide Preview
          • Download PDF
          • Export Citation
            Skin pigmentation is imparted by melanin and is crucial for photoprotection against UVR. Melanin is synthesized and packaged into melanosomes within melanocytes and is then transferred to keratinocytes (KCs). Although the molecular players involved in melanogenesis have been extensively studied, those underlying melanin transfer remain unclear. Previously, our group proposed that coupled exocytosis/phagocytosis is the predominant mechanism of melanin transfer in human skin and showed an essential role for RAB11B and the exocyst tethering complex in this process.
            RAB3A Regulates Melanin Exocytosis and Transfer Induced by Keratinocyte-Conditioned Medium
          • Original Article
            Open Access

            Identification of Keratinocyte Mitogens: Implications for Hyperproliferation in Psoriasis and Atopic Dermatitis

            JID Innovations
            Vol. 2Issue 1100066Published online: October 21, 2021
            • Hanna Niehues
            • Gijs Rikken
            • Ivonne M.J.J. van Vlijmen-Willems
            • Diana Rodijk-Olthuis
            • Piet E.J. van Erp
            • Patrick L.J.M. Zeeuwen
            • and others
            Cited in Scopus: 0
            • Preview Hide Preview
            • Download PDF
            • Export Citation
              Psoriasis and atopic dermatitis are chronic inflammatory skin diseases characterized by keratinocyte (KC) hyperproliferation and epidermal acanthosis (hyperplasia). The milieu of disease-associated cytokines and soluble factors is considered a mitogenic factor; however, pinpointing the exact mitogens in this complex microenvironment is challenging. We employed organotypic human epidermal equivalents, faithfully mimicking native epidermal proliferation and stratification, to evaluate the proliferative effects of a broad panel of (literature-based) potential mitogens.
              Identification of Keratinocyte Mitogens: Implications for Hyperproliferation in Psoriasis and Atopic Dermatitis
            • Original Article
              Open Access

              Lipid Droplet Proteins in Acne Skin: A Sound Target for the Maintenance of Low Comedogenic Sebum and Acne-Prone Skin Health

              JID Innovations
              Vol. 1Issue 4100057Published online: September 16, 2021
              • Olivier Sorg
              • Thérèse Nocera
              • Fabienne Fontao
              • Nathalie Castex-Rizzi
              • Lucile Garidou
              • Christophe Lauze
              • and others
              Cited in Scopus: 0
              • Preview Hide Preview
              • Download PDF
              • Export Citation
                In adipocytes and sebocytes, lipid droplet proteins control the storage of lipids in organized droplets and their release on demand. The contribution of lipid droplet proteins to the pathogenesis of acne is plausible because they control the levels of comedogenic free fatty acids. The expression of two lipid droplet proteins, CIDEA and PLIN2, was analyzed in the skin of patients with acne by immunohistochemistry and western blotting. The design of clinical protocols allowed correlating the expression of CIDEA and PLIN2 with both comedogenesis and the release of free fatty acids.
                Lipid Droplet Proteins in Acne Skin: A Sound Target for the Maintenance of Low Comedogenic Sebum and Acne-Prone Skin Health
              • Original Article
                Open Access

                Deletion of TNFAIP6 Gene in Human Keratinocytes Demonstrates a Role for TSG-6 to Retain Hyaluronan Inside Epidermis

                JID Innovations
                Vol. 1Issue 4100054Published online: August 23, 2021
                • Céline Evrard
                • Emilie Faway
                • Evelyne De Vuyst
                • Olivier Svensek
                • Valérie De Glas
                • David Bergerat
                • and others
                Cited in Scopus: 0
                • Preview Hide Preview
                • Download PDF
                • Export Citation
                  TSG-6 is a soluble protein secreted in the extracellular matrix by various cell types in response to inflammatory stimuli. TSG-6 interacts with extracellular matrix molecules, particularly hyaluronan (HA), and promotes cutaneous wound closure in mice. Between epidermal cells, the discrete extracellular matrix contains HA and a tiny amount of TSG-6. However, challenges imposed to keratinocytes in reconstructed human epidermis revealed strong induction of TSG-6 expression, after exposure to T helper type 2 cytokines to recapitulate the atopic dermatitis phenotype or after fungal infection that causes secretion of cytokines and antimicrobial peptides.
                  Deletion of TNFAIP6 Gene in Human Keratinocytes Demonstrates a Role for TSG-6 to Retain Hyaluronan Inside Epidermis
                • Original Article
                  Open Access

                  Hair Follicle Grafting Therapy Promotes Re-Emergence of Critical Skin Components in Chronic Nonhealing Wounds

                  JID Innovations
                  Vol. 1Issue 3100041Published online: July 8, 2021
                  • Dyuti Saha
                  • Sujaya Thannimangalath
                  • Leelavathy Budamakuntla
                  • Eswari Loganathan
                  • Colin Jamora
                  Cited in Scopus: 0
                  • Preview Hide Preview
                  • Download PDF
                  • Export Citation
                    An exploding public health crisis is the exponential growth in the incidence of chronic nonhealing ulcers associated with diseases such as diabetes. Various modalities have been developed to stimulate wound closure that is otherwise recalcitrant to standard clinical treatments. However, these approaches primarily focus on the process of re-epithelialization and are often deficient in regenerating the full spectrum of structures necessary for normal skin function. Autologous hair follicle grafting is a recent therapy to stimulate the closure of such nonhealing wounds, and we observed effects beyond the epidermis to other important components of the dermis.
                    Hair Follicle Grafting Therapy Promotes Re-Emergence of Critical Skin Components in Chronic Nonhealing Wounds
                  • Review
                    Open Access

                    Cracking the Skin Barrier: Liquid-Liquid Phase Separation Shines under the Skin

                    JID Innovations
                    Vol. 1Issue 3100036Published online: July 5, 2021
                    • Alexa Regina Chua Avecilla
                    • Felipe Garcia Quiroz
                    Cited in Scopus: 0
                    • Preview Hide Preview
                    • Download PDF
                    • Export Citation
                      Central to forming and sustaining the skin’s barrier, epidermal keratinocytes (KCs) fluxing to the skin surface undergo a rapid and enigmatic transformation into flat, enucleated squames. At the crux of this transformation are intracellular keratohyalin granules (KGs) that suddenly disappear as terminally differentiating KCs transition to the cornified skin surface. Defects in KGs have long been linked to skin barrier disorders. Through the biophysical lens of liquid-liquid phase separation (LLPS), these enigmatic KGs recently emerged as liquid-like membraneless organelles whose assembly and subsequent pH-triggered disassembly drive squame formation.
                      Cracking the Skin Barrier: Liquid-Liquid Phase Separation Shines under the Skin
                    • Original Article
                      Open Access

                      Kininogen–Nitric Oxide Signaling at Nearby Nonexcited Acupoints after Long-Term Stimulation

                      JID Innovations
                      Vol. 1Issue 3100038Published online: June 24, 2021
                      • Ting Wang
                      • Geng Zhu
                      • Liyue Qin
                      • Qian Wang
                      • Chen She
                      • Dongsheng Xu
                      • and others
                      Cited in Scopus: 0
                      • Preview Hide Preview
                      • Download PDF
                      • Export Citation
                        Acupuncture treatment is based on acupoint stimulation; however, the biological basis is not understood. We stimulated one acupoint with catgut embedding for 8 weeks and then used isobaric tags for relative and absolute quantitation to screen proteins with altered expression in adjacent acupoints of Sprague Dawley rats. We found that kininogen expression was significantly upregulated in the stimulated and the nonstimulated adjacent acupoints along the same meridian. The enhanced kininogen expression was meridian dependent and was most apparent among small vessels in the subcutaneous layer.
                        Kininogen–Nitric Oxide Signaling at Nearby Nonexcited Acupoints after Long-Term Stimulation
                      • Review
                        Open Access

                        Seeing through the Skin: Photoacoustic Tomography of Skin Vasculature and Beyond

                        JID Innovations
                        Vol. 1Issue 3100039Published online: June 24, 2021
                        • Daiwei Li
                        • Lucas Humayun
                        • Emelina Vienneau
                        • Tri Vu
                        • Junjie Yao
                        Cited in Scopus: 0
                        • Preview Hide Preview
                        • Download PDF
                        • Export Citation
                          Skin diseases are the most common human diseases and manifest in distinct structural and functional changes to skin tissue components such as basal cells, vasculature, and pigmentation. Although biopsy is the standard practice for skin disease diagnosis, it is not sufficient to provide in vivo status of the skin and highly depends on the timing of diagnosis. Noninvasive imaging technologies that can provide structural and functional tissue information in real time would be invaluable for skin disease diagnosis and treatment evaluation.
                          Seeing through the Skin: Photoacoustic Tomography of Skin Vasculature and Beyond
                        • Original Article
                          Open Access

                          Peroxisomal Fatty Acid Oxidation and Glycolysis Are Triggered in Mouse Models of Lesional Atopic Dermatitis

                          JID Innovations
                          Vol. 1Issue 3100033Published online: June 14, 2021
                          • Petra Pavel
                          • Géraldine Leman
                          • Martin Hermann
                          • Christian Ploner
                          • Thomas O. Eichmann
                          • Deborah Minzaghi
                          • and others
                          Cited in Scopus: 0
                          • Preview Hide Preview
                          • Download PDF
                          • Export Citation
                            Alterations of the lipid profile of the stratum corneum have an important role in the pathogenesis of atopic dermatitis (AD) because they contribute to epidermal barrier impairment. However, they have not previously been envisioned as a cellular response to altered metabolic requirements in AD epidermis. In this study, we report that the lipid composition in the epidermis of flaky tail, that is, ft/ft mice mimics that of human lesional AD (ADL) epidermis, both showing a shift toward shorter lipid species.
                            Peroxisomal Fatty Acid Oxidation and Glycolysis Are Triggered in Mouse Models of Lesional Atopic Dermatitis
                          • Original Article
                            Open Access

                            Dehydrated Human Amniotic Membrane Inhibits Myofibroblast Contraction through the Regulation of the TGFβ‒SMAD Pathway In Vitro

                            JID Innovations
                            Vol. 1Issue 2100020Published online: May 5, 2021
                            • Sarah E. Moreno
                            • Michelle Massee
                            • Thomas J. Koob
                            Cited in Scopus: 0
                            • Preview Hide Preview
                            • Download PDF
                            • Export Citation
                              Excessive fibrosis affects more than 100 million patients yearly, leading to the accumulation of extracellular matrix that compromises tissue architecture and impedes its function. Intrinsic properties of the amniotic membrane have alluded to its potential to inhibit excessive fibrosis; therefore, this study aimed to investigate the effects of dehydrated human amnion/chorion membrane (dHACM) on dermal fibroblasts and their role in fibrotic pathways. Human dermal fibroblasts were stimulated with TGFβ1, triggering myofibroblast-like characteristics in vitro.
                              Dehydrated Human Amniotic Membrane Inhibits Myofibroblast Contraction through the Regulation of the TGFβ‒SMAD Pathway In Vitro
                            • Original Article
                              Open Access

                              Topical Treatment of Human Skin and Cultured Keratinocytes with High-Dose Spironolactone Reduces XPB Expression and Induces Toxicity

                              JID Innovations
                              Vol. 1Issue 3100023Published online: May 5, 2021
                              • M. Alexandra Carpenter
                              • Michael G. Kemp
                              Cited in Scopus: 0
                              • Preview Hide Preview
                              • Download PDF
                              • Export Citation
                                Spironolactone (SP) is used to treat a variety of disparate disease states ranging from heart failure to acne through antagonism of the mineralocorticoid and androgen receptors. Although normally taken as an oral medication, recent studies have explored the topical application of SP onto the skin. However, because SP induces the proteolytic degradation of the XPB protein, which plays critical roles in DNA repair and transcription, there may be safety concerns with the use of topical SP. In this study, we show that the topical application of a high concentration of either SP or its metabolite canrenone onto human skin ex vivo lowers XPB protein levels and induces toxic responses in the epidermis.
                                Topical Treatment of Human Skin and Cultured Keratinocytes with High-Dose Spironolactone Reduces XPB Expression and Induces Toxicity
                              • Original Article
                                Open Access

                                Characterization of Human Keratinocyte Cell Lines for Barrier Studies

                                JID Innovations
                                Vol. 1Issue 2100018Published online: April 27, 2021
                                • Mary C. Moran
                                • Radha P. Pandya
                                • Kimberly A. Leffler
                                • Takeshi Yoshida
                                • Lisa A. Beck
                                • Matthew G. Brewer
                                Cited in Scopus: 0
                                • Preview Hide Preview
                                • Download PDF
                                • Export Citation
                                  Epidermal cell models are critical for studying skin biology. The gold standard used by the scientific community has historically been primary cell cultures from discarded tissue, typically from neonates (foreskin). Although directly applicable to humans, this system suffers from multiple issues, including substantial donor-to-donor variability and a finite number of divisions in culture. As such, we have identified a faithful alternative called N/TERT2G cells. These cells show many of the characteristics of primary cells, including barrier formation, differentiation kinetics and/or protein expression, and pathogenesis.
                                  Characterization of Human Keratinocyte Cell Lines for Barrier Studies
                                • Original Article
                                  Open Access

                                  Determination of Chemical Irritation Potential Using a Defined Gene Signature Set on Tissue-Engineered Human Skin Equivalents

                                  JID Innovations
                                  Vol. 1Issue 2100011Published online: March 15, 2021
                                  • Amy L. Harding
                                  • Craig Murdoch
                                  • Simon Danby
                                  • Md Zobaer Hasan
                                  • Hirofumi Nakanishi
                                  • Tetsuo Furuno
                                  • and others
                                  Cited in Scopus: 0
                                  • Preview Hide Preview
                                  • Download PDF
                                  • Export Citation
                                    There are no physical or visual manifestations that define skin sensitivity or irritation; a subjective diagnosis is made on the basis of the evaluation of clinical presentations, including burning, prickling, erythema, and itching. Adverse skin reaction in response to topically applied products is common and can limit the use of dermatological or cosmetic products. The purpose of this study was to evaluate the use of human skin equivalents based on immortalized skin keratinocytes and evaluate the potential of a 22-gene panel in combination with multivariate analysis to discriminate between chemicals known to act as irritants and those that do not.
                                    Determination of Chemical Irritation Potential Using a Defined Gene Signature Set on Tissue-Engineered Human Skin Equivalents
                                  • Original Article
                                    Open Access

                                    Unlocking the Mechanisms of Cutaneous Adverse Drug Reactions: Activation of the Phosphatidylinositol 3-Kinase/Protein Kinase B Pathway by EGFR Inhibitors Triggers Keratinocyte Differentiation and Polarization of Epidermal Immune Responses

                                    JID Innovations
                                    Vol. 1Issue 2100009Published online: March 5, 2021
                                    • Thomas Ondet
                                    • Pierre-François Roux
                                    • Mario Monshouwer
                                    • Georgios N. Stamatas
                                    Cited in Scopus: 0
                                    • Preview Hide Preview
                                    • Download PDF
                                    • Export Citation
                                      EGFR inhibitors used in oncology therapy modify the keratinocyte differentiation processes, impairing proper skin barrier formation and leading to cutaneous adverse drug reactions. To uncover the molecular signatures associated with cutaneous adverse drug reactions, we applied phosphoproteomic and transcriptomic assays on reconstructed human epidermis tissues exposed to a therapeutically relevant concentration of afatinib, a second-generation EGFR inhibitor. After drug exposure, we observed activation of the phosphatidylinositol 3-kinase/protein kinase B pathway associated with an increased expression of gene families involved in keratinocyte differentiation, senescence, oxidative stress, and alterations in the epidermal immune-related markers.
                                      Unlocking the Mechanisms of Cutaneous Adverse Drug Reactions: Activation of the Phosphatidylinositol 3-Kinase/Protein Kinase B Pathway by EGFR Inhibitors Triggers Keratinocyte Differentiation and Polarization of Epidermal Immune Responses
                                    Page 1 of 1
                                    • Home
                                    • Articles & Issues
                                    • Articles In Press
                                    • Current Issue
                                    • Issues in Progress
                                    • List of Issues
                                    • Collections
                                    • Atopic Disease
                                    • Cancer
                                    • Cell Biology
                                    • Clinical & Translational Research
                                    • Cover Gallery
                                    • Genetic Disease
                                    • Immunity
                                    • Melanoma
                                    • New Methodology
                                    • Non-Melanoma Skin Cancer
                                    • Photobiology
                                    • Psoriasis
                                    • Training Physician Scientists
                                    • Authors/Reviewers
                                    • Instructions for Authors
                                    • Submit a Manuscript
                                    • Thank You, Reviewers
                                    • Editorial Board
                                    • Permissions
                                    • Researcher Academy
                                    • -->
                                    • Journal Info
                                    • About the Journal
                                    • Advertisers
                                    • Contact Us
                                    • New Content Alerts
                                    • SID
                                    • SID Website
                                    • Join SID
                                    • Annual Meeting
                                    • Academic Industry Partnership
                                    • ESDR
                                    • ESDR Website
                                    • Join ESDR
                                    • Awards
                                    • Events
                                    • Media
                                    • Education
                                    • Companion Titles
                                    • Journal of Investigative Dermatology
                                    • Journal of Investigative Dermatology Symposium Proceedings
                                    • Follow Us
                                    • Facebook
                                    • Twitter

                                    The content on this site is intended for healthcare professionals.



                                    We use cookies to help provide and enhance our service and tailor content. To update your cookie settings, please visit the Cookie Preference Center for this site.
                                    Copyright © 2023 Elsevier Inc. except certain content provided by third parties.

                                    • Privacy Policy  
                                    • Terms and Conditions  
                                    • Accessibility  
                                    • Help & Contact

                                    RELX