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Hanin, G.* ; Yayon, N.* ; Tzur, Y.* ; Haviv, R.* ; Bennett, E.R.* ; Udi, S.* ; Krishnamoorthy, Y.R.* ; Kotsiliti, E. ; Zangen, R.* ; Efron, B.* ; Tam, J.* ; Pappo, O.* ; Shteyer, E.* ; Pikarsky, E.* ; Heikenwälder, M. ; Greenberg, D.S.* ; Soreq, H.*

miRNA-132 induces hepatic steatosis and hyperlipidaemia by synergistic multitarget suppression.

Gut 67, 1124-1134 (2017)
Publ. Version/Full Text DOI PMC
Open Access Gold (Paid Option)
Creative Commons Lizenzvertrag
Skin affections after sulfur mustard (SM) exposure include erythema, blister formation and severe inflammation. An antidote or specific therapy does not exist. Anti-inflammatory compounds as well as substances counteracting SM-induced cell death are under investigation. In this study, we investigated the benzylisoquinoline alkaloide berberine (BER), a metabolite in plants like berberis vulgaris, which is used as herbal pharmaceutical in Asian countries, against SM toxicity using a well-established in vitro approach. Keratinocyte (HaCaT) mono-cultures (MoC) or HaCaT/THP-1 co-cultures (CoC) were challenged with 100, 200 or 300 mM SM for 1 h. Post-exposure, both MoC and CoC were treated with 10, 30 or 50 mu M BER for 24 h. At that time, supernatants were collected and analyzed both for interleukine (IL) 6 and 8 levels and for content of adenylate-kinase (AK) as surrogate marker for cell necrosis. Cells were lysed and nucleosome formation as marker for late apoptosis was assessed. In parallel, AK in cells was determined for normalization purposes. BER treatment did not influence necrosis, but significantly decreased apoptosis. Anti-inflammatory effects were moderate, but also significant, primarily in CoC. Overall, BER has protective effects against SM toxicity in vitro. Whether this holds true should be evaluated in future in vivo studies.
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Publication type Article: Journal article
Document type Scientific Article
Corresponding Author
Keywords Fatty Liver ; Nonalcoholic Steatohepatitis; Cell-line Thp-1; In-vitro; Hacat Keratinocytes; Alkaloid Berberine; Dendritic Cells; Injury; Skin; Sensitization; Expression; Toxicity
ISSN (print) / ISBN 0017-5749
e-ISSN 1468-3288
Journal Gut (eGut)
Quellenangaben Volume: 67, Issue: 6, Pages: 1124-1134 Article Number: , Supplement: ,
Publisher BMJ Publishing Group
Publishing Place Elsevier House, Brookvale Plaza, East Park Shannon, Co, Clare, 00000, Ireland
Non-patent literature Publications
Reviewing status Peer reviewed
Institute(s) Institute of Virology (VIRO)