2020
DOI: 10.1111/bjd.19552
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A novel nondrug SFRP1 antagonist inhibits catagen development in human hair follicles ex vivo

Abstract: Prevalence, correlates and clinical usefulness of antibodies to RNA polymerase III in systemic sclerosis: a cross-sectional analysis of data from an Australian cohort.

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Cited by 8 publications
(7 citation statements)
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“…The point photograph presented some overlapping genes in multiple compared groups especially back skin compared with other skin sites, including TNN, COL11A1, SFRP1, COL6A5, INHBA, APOA1, IGF1 and SPARCL1. Notably, TNN, called tenascin-N(W), is lager domain glycoprotein that has the potential to modify cell adhesion and typically contribute to cell motility (Chiquet-Ehrismann and Tucker, 2011); COL11A1, an extracellular matrix structural constituent, comprises a subclass of regulatory collagens fibrillogenesis that synergistically assemble other types of collagen such as collagen I, determining fibril structure, fibril organization and functional traits (Smith and Birk, 2012; Sun et al, 2020); SFRP1, a member of secretory glycoprotein SFRP family, is regarded as one of the main classes of macromolecules making up the ECM elements and is reported to be an antagonist that inhibits human hair follicles recession (Bertolini et al, 2021; Jiang et al, 2022); INHBA is a member of TGFβ superfamily and is modified by AP1 expression (Ham et al, 2021). Subsequently, we implemented KEGG analysis in the compared groups (Figure 5—figure supplement 1F, G) and presented dominant enrichment pathways such as ECM-receptor interaction, focal adhesion, protein digestion and adsorption and TGF-beta signaling pathway.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…The point photograph presented some overlapping genes in multiple compared groups especially back skin compared with other skin sites, including TNN, COL11A1, SFRP1, COL6A5, INHBA, APOA1, IGF1 and SPARCL1. Notably, TNN, called tenascin-N(W), is lager domain glycoprotein that has the potential to modify cell adhesion and typically contribute to cell motility (Chiquet-Ehrismann and Tucker, 2011); COL11A1, an extracellular matrix structural constituent, comprises a subclass of regulatory collagens fibrillogenesis that synergistically assemble other types of collagen such as collagen I, determining fibril structure, fibril organization and functional traits (Smith and Birk, 2012; Sun et al, 2020); SFRP1, a member of secretory glycoprotein SFRP family, is regarded as one of the main classes of macromolecules making up the ECM elements and is reported to be an antagonist that inhibits human hair follicles recession (Bertolini et al, 2021; Jiang et al, 2022); INHBA is a member of TGFβ superfamily and is modified by AP1 expression (Ham et al, 2021). Subsequently, we implemented KEGG analysis in the compared groups (Figure 5—figure supplement 1F, G) and presented dominant enrichment pathways such as ECM-receptor interaction, focal adhesion, protein digestion and adsorption and TGF-beta signaling pathway.…”
Section: Resultsmentioning
confidence: 99%
“…The copyright holder for this preprint this version posted February 18, 2023. ; https://doi.org/10.1101/2023.02.17.528908 doi: bioRxiv preprint (Bertolini et al, 2021;Jiang et al, 2022); INHBA is a member of TGFβ superfamily and is modified by AP1 expression (Ham et al, 2021). Subsequently, we implemented KEGG analysis in the compared groups (Figure 5-figure supplement 1F, G) and presented dominant enrichment pathways such as ECM-receptor interaction, focal adhesion, protein digestion and adsorption and TGF-beta signaling pathway.…”
Section: Heterogeneity Of the Fibroblastmentioning
confidence: 99%
“…For IGF‐1 [32] and FGF‐7 [55] expression, cryosections were fixed in acetone at −20°C and pre‐incubated with 2% normal goat serum in TNB buffer (Tris‐HCl + NaCl + Casein) or 10% NGS for 30 min at room temperature (RT) prior to overnight incubation at 4°C with a rabbit anti‐human IGF‐1 primary antibody (1/200 in 2% NGS, Abcam) or a rabbit anti‐human FGF‐7 primary antibody (1/150 in 10% NGS, Abcam). Secondary antibody incubation was performed at RT for 45 min using a goat anti‐rabbit Alexa Fluor 488 (1/400 in 2% NGS (IGF‐1) or 1/750 in 10% NGS (FGF‐7), Invitrogen).…”
Section: Methodsmentioning
confidence: 99%
“…The latter is sustained by the expression of the extracellular matrix protein, versican and the expression and activity of alkaline phosphatase in the hair follicle dermal papilla [27][28][29][30]. Notably, dermal papilla inductivity is linked to the production of Wnt molecules that stimulate the proliferation of hair matrix keratinocytes [27,31,32]. Importantly, DP inductivity is decreased in androgenetic alopecia and telogen effluvium [33].…”
Section: Introductionmentioning
confidence: 99%
“…This has identified a novel regulatory principle in human hair growth control and has encouraged the development of non-immunosuppressive SFRP1-inhibitory agents as a novel class of human hair growth promoters. 67,179 Instead, given the recently appreciated pathogenic role of excessive epidermal Wnt activity in psoriatic lesions, 180,181 topically applicable drugs that up-regulate the production of endogenous Wnt inhibitors in human skin, such as SFRP1 and DKK1, 68…”
Section: Tr Ans L Ational Rele Van Ce and Con Cluding Remark Smentioning
confidence: 99%