TY - JOUR
T1 - Analysis of gene expression profiles in tympanic membrane following perforation using PCR Array in rats-Preliminary investigation
AU - Hassmann-Poznańska, Elzbieta
AU - Taranta, Andrzej
AU - Bialuk, Izabela
AU - Poznańska, Maria
AU - Zajaczkiewicz, Hanna
AU - Winnicka, Maria Małgorzata
PY - 2013/10/1
Y1 - 2013/10/1
N2 - Objectives: The goal of this work was to identify genes, known to be involved in the skin wound healing, that express differentially in the healthy and injured tympanic membrane (TM), and designate the molecules potentially beneficial for treatment of TM perforation. The molecular mechanisms controlling the course of TM regeneration are far from being elucidated. Methods: Twenty rats had their tympanic membranes perforated, while four served as a control. Animals were sacrificed on either days 1, 2, 3, 5 and 10 post injury, and TMs were immediately dissected and frozen in liquid nitrogen. Total TM RNA was isolated and reversely transcribed. qPCR was performed using Rat Wound Healing RT2 Profiler PCR Array (QIAGEN) containing primers for 84 genes. Results: Statistically significant changes in the expression of 42 genes were found in various stages of TM healing. The increased expression of genes taking part in the inflammatory reaction (interleukin 6, granulocyte and macrophage chemotactic proteins) was observed from day 2. The expression of several genes of extracellular matrix components and their remodeling enzymes was also changed. Among growth factor genes: Vegfa, Igf1 and Hbegf showed increased expression at the beginning of the healing process, while Hgf expression was highest on day 3. Conclusions: Several changes in the expression of genes involved in remodeling of extracellular matrix point to important role of connective tissue in TM healing. The molecules accelerating this process, like HbEGF and HGF, seem to be good candidates for further evaluation of their possible use in clinical treatment.
AB - Objectives: The goal of this work was to identify genes, known to be involved in the skin wound healing, that express differentially in the healthy and injured tympanic membrane (TM), and designate the molecules potentially beneficial for treatment of TM perforation. The molecular mechanisms controlling the course of TM regeneration are far from being elucidated. Methods: Twenty rats had their tympanic membranes perforated, while four served as a control. Animals were sacrificed on either days 1, 2, 3, 5 and 10 post injury, and TMs were immediately dissected and frozen in liquid nitrogen. Total TM RNA was isolated and reversely transcribed. qPCR was performed using Rat Wound Healing RT2 Profiler PCR Array (QIAGEN) containing primers for 84 genes. Results: Statistically significant changes in the expression of 42 genes were found in various stages of TM healing. The increased expression of genes taking part in the inflammatory reaction (interleukin 6, granulocyte and macrophage chemotactic proteins) was observed from day 2. The expression of several genes of extracellular matrix components and their remodeling enzymes was also changed. Among growth factor genes: Vegfa, Igf1 and Hbegf showed increased expression at the beginning of the healing process, while Hgf expression was highest on day 3. Conclusions: Several changes in the expression of genes involved in remodeling of extracellular matrix point to important role of connective tissue in TM healing. The molecules accelerating this process, like HbEGF and HGF, seem to be good candidates for further evaluation of their possible use in clinical treatment.
KW - Extracellular matrix remodeling
KW - Gene expression profiles
KW - Growth factors
KW - Rats
KW - Regeneration of tympanic membrane
KW - Wound healing
UR - http://www.scopus.com/inward/record.url?scp=84884290973&partnerID=8YFLogxK
U2 - 10.1016/j.ijporl.2013.08.009
DO - 10.1016/j.ijporl.2013.08.009
M3 - Journal article
C2 - 24012216
AN - SCOPUS:84884290973
SN - 0165-5876
VL - 77
SP - 1753
EP - 1759
JO - International Journal of Pediatric Otorhinolaryngology
JF - International Journal of Pediatric Otorhinolaryngology
IS - 10
ER -