» Articles » PMID: 27465141

Identification of Differentially Regulated Genes in Human Patent Ductus Arteriosus

Overview
Specialty Biology
Date 2016 Jul 29
PMID 27465141
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

In order to identify differentially expressed genes that are specific to the ductus arteriosus, 18 candidate genes were evaluated in matched ductus arteriosus and aortic samples from infants with coarctation of the aorta. The cell specificity of the gene's promoters was assessed by performing transient transfection studies in primary cells derived from several patients. Segments of ductus arteriosus and aorta were isolated from infants requiring repair for coarctation of the aorta and used for mRNA quantitation and culturing of cells. Differences in expression were determined by quantitative PCR using the ΔΔCt method. Promoter regions of six of these genes were cloned into luciferase reporter plasmids for transient transfection studies in matched human ductus arteriosus and aorta cells. Transcription factor AP-2b and phospholipase A2 were significantly up-regulated in ductus arteriosus compared to aorta in whole tissues and cultured cells, respectively. In transient transfection experiments, Angiotensin II type 1 receptor and Prostaglandin E receptor 4 promoters consistently gave higher expression in matched ductus arteriosus versus aorta cells from multiple patients. Taken together, these results demonstrate that several genes are differentially expressed in ductus arteriosus and that their promoters may be used to drive ductus arteriosus-enriched transgene expression.

Citing Articles

Association of the rs7557402 Polymorphism with Hemodynamically Significant Patent Ductus Arteriosus Closure Failure in Premature Newborns under Pharmacological Treatment with Ibuprofen.

Rogel-Ayala D, Munoz-Medina J, Vicente-Juarez V, Grether-Gonzalez P, Morales-Barquet D, Martinez-Garcia A Diagnostics (Basel). 2023; 13(15).

PMID: 37568921 PMC: 10417126. DOI: 10.3390/diagnostics13152558.


Transcriptional profiles in the chicken ductus arteriosus during hatching.

Akaike T, Shinjo S, Ohmori E, Kajimura I, Goda N, Minamisawa S PLoS One. 2019; 14(3):e0214139.

PMID: 30897181 PMC: 6428269. DOI: 10.1371/journal.pone.0214139.


Dark-colored maple syrup treatment induces S-phase cell cycle arrest via reduced proliferating cell nuclear antigen expression in colorectal cancer cells.

Yamamoto T, Nishita T, Taga A Oncol Lett. 2019; 17(3):2713-2720.

PMID: 30854045 PMC: 6365951. DOI: 10.3892/ol.2019.9928.


Novel drug targets for ductus arteriosus manipulation: Looking beyond prostaglandins.

Shelton E, Singh G, Nichols C Semin Perinatol. 2018; 42(4):221-227.

PMID: 29880312 PMC: 6064654. DOI: 10.1053/j.semperi.2018.05.004.

References
1.
Huang J, Cheng L, Li J, Chen M, Zhou D, Lu M . Myocardin regulates expression of contractile genes in smooth muscle cells and is required for closure of the ductus arteriosus in mice. J Clin Invest. 2008; 118(2):515-25. PMC: 2176191. DOI: 10.1172/JCI33304. View

2.
Yajima I, Colombo S, Puig I, Champeval D, Kumasaka M, Belloir E . A subpopulation of smooth muscle cells, derived from melanocyte-competent precursors, prevents patent ductus arteriosus. PLoS One. 2013; 8(1):e53183. PMC: 3561373. DOI: 10.1371/journal.pone.0053183. View

3.
Treszl A, Szabo M, Dunai G, Nobilis A, Kocsis I, Machay T . Angiotensin II type 1 receptor A1166C polymorphism and prophylactic indomethacin treatment induced ductus arteriosus closure in very low birth weight neonates. Pediatr Res. 2003; 54(5):753-5. DOI: 10.1203/01.PDR.0000088016.67117.39. View

4.
Kajino H, Chen Y, Seidner S, Waleh N, Mauray F, Roman C . Factors that increase the contractile tone of the ductus arteriosus also regulate its anatomic remodeling. Am J Physiol Regul Integr Comp Physiol. 2001; 281(1):R291-301. DOI: 10.1152/ajpregu.2001.281.1.R291. View

5.
Waleh N, Barrette A, Dagle J, Momany A, Jin C, Hills N . Effects of Advancing Gestation and Non-Caucasian Race on Ductus Arteriosus Gene Expression. J Pediatr. 2015; 167(5):1033-41.e2. PMC: 4661123. DOI: 10.1016/j.jpeds.2015.07.011. View