Improved Growth Patterns in Cystic Fibrosis Mice after Loss of Histone Deacetylase 6.

Abstract

Growth failure in cystic fibrosis (CF) patients has been well-documented and shown to correlate with poorer disease outcomes. This observation is also true in CF animal models, including mouse, pig, rat, and ferret. The etiology underlying growth deficits is unknown, and our previous work demonstrated reduced tubulin acetylation in CF cell models and tissue that is correctable by inhibition of histone deacetylase-6 (HDAC6). Here, we hypothesize that loss of HDAC6 will improve growth phenotype in a CF mouse model. Hdac6 knockout mice were crossed with F508del (CF) mice to generate F508del/Hdac6 (CF/HDA) mice. Growth, fat deposits, survival, and bioelectric measurements were analyzed. CF/HDA mice displayed improvements in length and weight with no correction of CFTR function. Mechanistically, Igf1 levels likely account for increased length and improvements in fertility. Weight gain is attributed to increased fat deposits potentially mediated by increased adipocyte differentiation. CF-related growth deficits can be improved via inhibition of HDAC6, further implicating it as a potential therapeutic target for CF.

• Authors: Sharon M Rymut, Deborah A Corey, Dana M Valerio, Bernadette O Erokwu, Chris A Flask, Thomas J Kelley, Craig A Hodges
• Journal: Scientific reports (Sci Rep) Vol. 7 Issue 1 Pg. 3676 (06 16 2017) ISSN: 2045-2322 [Electronic] England
• PMID: 28623308 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Biomarkers
• Cystic Fibrosis Transmembrane Conductance Regulator
• Hdac6 protein, mouse
• Histone Deacetylase 6

Topics

• Adiposity
• Animals
• Biomarkers
• Cystic Fibrosis (complications, genetics, metabolism)
• Cystic Fibrosis Transmembrane Conductance Regulator (genetics)
• Disease Models, Animal
• Female
• Fluorescent Antibody Technique
• Genetic Predisposition to Disease
• Growth Disorders (diagnosis, etiology, metabolism)
• Histone Deacetylase 6 (deficiency, genetics, metabolism)
• Male
• Mice
• Mice, Knockout