Human mesenchymal stem cells attenuate pulmonary hypertension induced by prenatal lipopolysaccharide treatment in rats. (October 2016)
- Record Type:
- Journal Article
- Title:
- Human mesenchymal stem cells attenuate pulmonary hypertension induced by prenatal lipopolysaccharide treatment in rats. (October 2016)
- Main Title:
- Human mesenchymal stem cells attenuate pulmonary hypertension induced by prenatal lipopolysaccharide treatment in rats
- Authors:
- Chou, Hsiu‐Chu
Lin, Willie
Chen, Chung‐Ming - Abstract:
- Summary: Intra‐amniotic injection of lipopolysaccharide (LPS) induces pulmonary hypertension in newborn rats. This study was designed to test whether human mesenchymal stem cells (MSCs) reduce pulmonary hypertension and alleviate cardiac hypertrophy in prenatal LPS‐treated rats. Pregnant Sprague‐Dawley rats were injected intraperitoneally with LPS (0.5 mg/kg per day) or untreated on gestational days 20 and 21. Human MSCs (3×10 5 cells and 1×10 6 cells) in 0.03 mL of normal saline (NS) were transplanted intratracheally on postnatal day 5. Four study groups were considered: normal, LPS+NS, LPS+MSCs (3×10 5 cells), and LPS+MSCs (1×10 6 cells). On postnatal day 14, lung and heart tissues were collected for measuring the arterial medial wall thickness (MWT) and β‐myosin heavy chain (β‐MHC) level as markers of pulmonary hypertension and cardiac hypertrophy, respectively. The LPS+NS group exhibited a significantly higher right ventricle (RV)/[left ventricle (LV)+ interventricular septum (IVS)] thickness ratio and MWT, a greater cardiomyocyte width, a greater number of cardiomyocyte nuclei per squared millimeter, and higher β‐MHC expression than those observed in the normal group. Human MSC transplantation (3×10 5 cells and 1×10 6 cells) in LPS‐treated rats reduced MWT and the RV/(LV+IVS) thickness ratio to normal levels. This improvement in right ventricular hypertrophy was accompanied by a decrease in toll‐like receptor 4 (TLR4), nuclear factor‐κB, and tumor necrosis factor‐αSummary: Intra‐amniotic injection of lipopolysaccharide (LPS) induces pulmonary hypertension in newborn rats. This study was designed to test whether human mesenchymal stem cells (MSCs) reduce pulmonary hypertension and alleviate cardiac hypertrophy in prenatal LPS‐treated rats. Pregnant Sprague‐Dawley rats were injected intraperitoneally with LPS (0.5 mg/kg per day) or untreated on gestational days 20 and 21. Human MSCs (3×10 5 cells and 1×10 6 cells) in 0.03 mL of normal saline (NS) were transplanted intratracheally on postnatal day 5. Four study groups were considered: normal, LPS+NS, LPS+MSCs (3×10 5 cells), and LPS+MSCs (1×10 6 cells). On postnatal day 14, lung and heart tissues were collected for measuring the arterial medial wall thickness (MWT) and β‐myosin heavy chain (β‐MHC) level as markers of pulmonary hypertension and cardiac hypertrophy, respectively. The LPS+NS group exhibited a significantly higher right ventricle (RV)/[left ventricle (LV)+ interventricular septum (IVS)] thickness ratio and MWT, a greater cardiomyocyte width, a greater number of cardiomyocyte nuclei per squared millimeter, and higher β‐MHC expression than those observed in the normal group. Human MSC transplantation (3×10 5 cells and 1×10 6 cells) in LPS‐treated rats reduced MWT and the RV/(LV+IVS) thickness ratio to normal levels. This improvement in right ventricular hypertrophy was accompanied by a decrease in toll‐like receptor 4 (TLR4), nuclear factor‐κB, and tumor necrosis factor‐α expression in the heart. Intratracheal human MSCs transplantation can attenuate pulmonary hypertension and right ventricular hypertrophy in prenatal LPS‐treated rats; this attenuation may be associated with suppression of TLR4 expression via paracrine pathways. … (more)
- Is Part Of:
- Clinical and experimental pharmacology and physiology. Volume 43:Number 10(2016:Oct.)
- Journal:
- Clinical and experimental pharmacology and physiology
- Issue:
- Volume 43:Number 10(2016:Oct.)
- Issue Display:
- Volume 43, Issue 10 (2016)
- Year:
- 2016
- Volume:
- 43
- Issue:
- 10
- Issue Sort Value:
- 2016-0043-0010-0000
- Page Start:
- 906
- Page End:
- 914
- Publication Date:
- 2016-10
- Subjects:
- β‐myosin heavy chain -- lipopolysaccharide -- medial wall thickness -- toll‐like receptor
Clinical pharmacology -- Periodicals
Pharmacology, Experimental -- Periodicals
Physiology, Experimental -- Periodicals
Physiology, Pathological -- Periodicals
615.1 - Journal URLs:
- http://www.blackwell-synergy.com/member/institutions/issuelist.asp?journal=cep ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/1440-1681.12604 ↗
- Languages:
- English
- ISSNs:
- 0305-1870
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3286.252000
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