1779 Cell Death Genes are Induced Immediately after Hypoxia-Reoxygenation (HR) in the Newborn Mouse Lung. (October 2012)
- Record Type:
- Journal Article
- Title:
- 1779 Cell Death Genes are Induced Immediately after Hypoxia-Reoxygenation (HR) in the Newborn Mouse Lung. (October 2012)
- Main Title:
- 1779 Cell Death Genes are Induced Immediately after Hypoxia-Reoxygenation (HR) in the Newborn Mouse Lung
- Authors:
- Wollen, EJ
Rognlien, AGW
Atneosen-Åsegg, M
Wright, MS
Bjørås, M
Saugstad, OD - Abstract:
- Abstract : Background and Aims: HR-injury can induce generation of reactive oxygen species which activate anti-/pro-apoptotic signalling in the cell or cause direct cell damage. The lungs of newborn neonates are susceptible to HR-injury. To explore underlying mechanisms, a temporal profile of a priori selected genes was performed. Methods: 84 C57BL/6 mice postnatal day 7 were randomized to 120 min of hypoxia (FiO2 0.08, n=64) or 180 min in air (C21, n=20). The hypoxia group was further randomized to 30 min reoxygenation with FiO2 0.60 (H60) or air (H2 1). Lung tissue was harvested after observation in air for 0, 150, 300 min or 3 days and 44 mRNA transcripts were analyzed by real-time PCR. Results: Bcl2, Bcl2l1, Bnip3 and Gadd45g were significantly up- regulated (p<0.05), and Ccnd1, Chek1 and Casp3 down-regulated in H60vsC21 and H2 1vsC21 (0 min). Apex1 and Apaf1 were also down-regulated in the comparison H60vsC21. After 150 min Apex1, Bcl2, Casp3, Ccnd1, Chek1 and Mutyh were down-regulated for H60vsC21 and H2 1vsC21. Bcl2 continued to be down-regulated in both comparisons (300 min). Gadd45g was only up-regulated in H60vsC21 after 150 and 300 min. No significant gene expression changes were observed after 3 days. Conclusion: HR-injury in the newborn lung induces an immediate alteration in the expression of both anti- ( Bcl2, Bcl2l1 ) and pro-apoptotic genes ( Bnip3, Apaf1, Apex1, Gadd45g ), while cell-cycle genes ( Ccnd1, Chek1 ) are suppressed. A suppression of Bcl2 fromAbstract : Background and Aims: HR-injury can induce generation of reactive oxygen species which activate anti-/pro-apoptotic signalling in the cell or cause direct cell damage. The lungs of newborn neonates are susceptible to HR-injury. To explore underlying mechanisms, a temporal profile of a priori selected genes was performed. Methods: 84 C57BL/6 mice postnatal day 7 were randomized to 120 min of hypoxia (FiO2 0.08, n=64) or 180 min in air (C21, n=20). The hypoxia group was further randomized to 30 min reoxygenation with FiO2 0.60 (H60) or air (H2 1). Lung tissue was harvested after observation in air for 0, 150, 300 min or 3 days and 44 mRNA transcripts were analyzed by real-time PCR. Results: Bcl2, Bcl2l1, Bnip3 and Gadd45g were significantly up- regulated (p<0.05), and Ccnd1, Chek1 and Casp3 down-regulated in H60vsC21 and H2 1vsC21 (0 min). Apex1 and Apaf1 were also down-regulated in the comparison H60vsC21. After 150 min Apex1, Bcl2, Casp3, Ccnd1, Chek1 and Mutyh were down-regulated for H60vsC21 and H2 1vsC21. Bcl2 continued to be down-regulated in both comparisons (300 min). Gadd45g was only up-regulated in H60vsC21 after 150 and 300 min. No significant gene expression changes were observed after 3 days. Conclusion: HR-injury in the newborn lung induces an immediate alteration in the expression of both anti- ( Bcl2, Bcl2l1 ) and pro-apoptotic genes ( Bnip3, Apaf1, Apex1, Gadd45g ), while cell-cycle genes ( Ccnd1, Chek1 ) are suppressed. A suppression of Bcl2 from 150 min and a continuous up-regulation of Gadd45g after hyperoxic reoxygenation may indicate early phase of DNA damage-induced apoptosis. … (more)
- Is Part Of:
- Archives of disease in childhood. Volume 97(2012)Supplement 2
- Journal:
- Archives of disease in childhood
- Issue:
- Volume 97(2012)Supplement 2
- Issue Display:
- Volume 97, Issue 2 (2012)
- Year:
- 2012
- Volume:
- 97
- Issue:
- 2
- Issue Sort Value:
- 2012-0097-0002-0000
- Page Start:
- A503
- Page End:
- A503
- Publication Date:
- 2012-10
- Subjects:
- Children -- Diseases -- Periodicals
Infants -- Diseases -- Periodicals
618.920005 - Journal URLs:
- http://adc.bmjjournals.com/ ↗
http://www.bmj.com/archive ↗ - DOI:
- 10.1136/archdischild-2012-302724.1779 ↗
- Languages:
- English
- ISSNs:
- 0003-9888
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
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- 18435.xml