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A potent antagonist antibody targeting connexin hemichannels alleviates Clouston syndrome symptoms in mutant mice.
- Source :
-
EBioMedicine [EBioMedicine] 2020 Jul; Vol. 57, pp. 102825. Date of Electronic Publication: 2020 Jun 15. - Publication Year :
- 2020
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Abstract
- Background: Numerous currently incurable human diseases have been causally linked to mutations in connexin (Cx) genes. In several instances, pathological mutations generate abnormally active Cx hemichannels, referred to also as "leaky" hemichannels. The goal of this study was to assay the in vivo efficacy of a potent antagonist antibody targeting Cx hemichannels.<br />Methods: We employed the antibody to treat Cx30 <superscript>A88V/A88V</superscript> adult mutant mice, the only available animal model of Clouston syndrome, a rare orphan disease caused by Cx30 p.A88V leaky hemichannels. To gain mechanistic insight into antibody action, we also performed patch clamp recordings, Ca <superscript>2+</superscript> imaging and ATP release assay in vitro.<br />Findings: Two weeks of antibody treatment sufficed to repress cell hyperproliferation in skin and reduce hypertrophic sebaceous glands (SGs) to wild type (wt) levels. These effects were obtained whether mutant mice were treated topically, by application of an antibody cream formulation, or systemically, by intraperitoneal antibody injection. Experiments with mouse primary keratinocytes and HaCaT cells revealed the antibody blocked Ca <superscript>2+</superscript> influx and diminished ATP release through leaky Cx30 p.A88V hemichannels.<br />Interpretation: Our results show anti-Cx antibody treatment was effective in vivo and sufficient to counteract the effects of pathological connexin expression in Cx30 <superscript>A88V/A88V</superscript> mice. In vitro experiments suggest antibodies gained control over leaky hemichannels and contributed to restoring epidermal homeostasis. Therefore, regulating cell physiology by antibodies targeting the extracellular domain of Cxs may enforce an entirely new therapeutic strategy. These findings support the further development of antibodies as drugs to address unmet medical needs for Cx-related diseases. FUND: Fondazione Telethon, GGP19148; University of Padova, SID/BIRD187130; Consiglio Nazionale delle Ricerche, DSB.AD008.370.003\TERABIO-IBCN; National Science Foundation of China, 31770776; Science and Technology Commission of Shanghai Municipality, 16DZ1910200.<br />Competing Interests: Declaration of Competing Interest Drs. F. Mammano, G. Yang and F. Zonta report a patent: “Fully human antibody specifically inhibiting connexin 26”, Inventors: Qu Z, Yang G, Mammano F, Zonta F, International application number: PCT/CN2016/109847, pending to ShanghaiTech University; and a patent: “Composition and Methods to treat Ectodermal Dysplasia 2, Clouston Type”, Inventors: Mammano F, Yang G, Zonta F, International Application No.: PCT/CN2019/088689, International Filing Date: 2019-05-28, pending to ShanghaiTech University. All other Authors have nothing to declare.<br /> (Copyright © 2020 The Author(s). Published by Elsevier B.V. All rights reserved.)
- Subjects :
- Adenosine Triphosphate genetics
Animals
Cell Proliferation drug effects
Connexin 30 antagonists & inhibitors
Connexin 30 immunology
Connexins antagonists & inhibitors
Connexins immunology
Disease Models, Animal
Ectodermal Dysplasia drug therapy
Ectodermal Dysplasia immunology
Epidermis drug effects
Epidermis growth & development
Epidermis metabolism
Gap Junctions genetics
Gap Junctions immunology
Gap Junctions pathology
Gene Expression Regulation drug effects
Humans
Keratinocytes drug effects
Keratinocytes immunology
Mice
Mutation genetics
Antibodies pharmacology
Connexin 30 genetics
Connexins genetics
Ectodermal Dysplasia genetics
Subjects
Details
- Language :
- English
- ISSN :
- 2352-3964
- Volume :
- 57
- Database :
- MEDLINE
- Journal :
- EBioMedicine
- Publication Type :
- Academic Journal
- Accession number :
- 32553574
- Full Text :
- https://doi.org/10.1016/j.ebiom.2020.102825