Rapamycin Inhibits Human Laryngotracheal Stenosis–derived Fibroblast Proliferation, Metabolism, and Function in Vitro. (9th March 2015)

• Record Type: Journal Article
• Authors: Namba, Daryan R.; Ma, Garret; Samad, Idris; Ding, Dacheng; Pandian, Vinciya; Powell, Jonathan D.; Horton, Maureen R.; Hillel, Alexander T.
• Is Part Of: Otolaryngology--head and neck surgery. Volume 152:Number 5(2015:May)
• Page Start: 881
• Page End: 888
• Publication Date: 2015-03-09
• Subjects: human -- trachea -- laryngotracheal stenosis -- rapamycin -- fibroblasts -- collagen; Head -- Surgery -- Periodicals; Neck -- Surgery -- Periodicals; Otolaryngology -- Periodicals; 617.51
• DOI: 10.1177/0194599815573708
• Languages: English
• ISSNs: 0194-5998

Abstract

Abstract : Objective: To determine if rapamycin inhibits the growth, function, and metabolism of human laryngotracheal stenosis (LTS)–derived fibroblasts. Study Design: Controlled in vitro study. Setting: Tertiary care hospital in a research university. Subjects and Methods: Fibroblasts isolated from biopsies of 5 patients with laryngotracheal stenosis were cultured. Cell proliferation, histology, gene expression, and cellular metabolism of LTS‐derived fibroblasts were assessed in 4 conditions: (1) fibroblast growth medium, (2) fibroblast growth medium with dimethylsulfoxide (DMSO), (3) fibroblast growth medium with 10 −10 M (low‐dose) rapamycin dissolved in DMSO, and (4) fibroblast growth medium with 10 −9 M (high‐dose) rapamycin dissolved in DMSO. Results: The LTS fibroblast count and DNA concentration were reduced after treatment with high‐dose rapamycin compared to DMSO ( P =. 0007) and normal ( P =. 0007) controls. Collagen I expression decreased after treatment with high‐dose rapamycin versus control ( P =. 0051) and DMSO ( P =. 0093) controls. Maximal respiration decreased to 68.6 pMoles of oxygen/min/10 mg/protein from 96.9 for DMSO ( P =. 0002) and 97.0 for normal ( P =. 0022) controls. Adenosine triphosphate (ATP) production decreased to 66.8 pMoles from 88.1 for DMSO ( P =. 0006) and 83.3 for normal ( P =. 0003) controls. Basal respiration decreased to 78.6 pMoles from 108 for DMSO ( P =. 0002) and 101 for normal ( P =. 0014) controls. Conclusions: Rapamycin demonstrated an anti‐fibroblast effect by significantly reducing the proliferation, metabolism, and collagen deposition of human LTS fibroblast in vitro. Rapamycin significantly decreased oxidative phosphorylation of LTS fibroblasts, suggesting at a potential mechanism for the reduced proliferation and differentiation. Furthermore, rapamycin's anti‐fibroblast effects indicate a promising adjuvant therapy for the treatment of laryngotracheal stenosis.