84 prolonged ventilation causes p27kip1 induced cell cycle arrest in newborn rat lung

84 prolonged ventilation causes p27kip1 induced cell cycle arrest in newborn rat lung

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ABSTRACT Background: I_n vitro_ studies have demonstrated that mechanical stretch can inhibit lung cell proliferation. This inhibition of cell growth may lead to reduction of alveolar formation and contribute to the development of bronchopulmonary dyplasia. Objective: To determine the effect of prolonged mechanical ventilation on cell-cycle regulation in a newborn rat model. Methods: 7-day old Wistar rats were ventilated with low/moderate tidal volume and room air for 24 h. Following ventilation arterial blood gas analysis was performed and the animal was killed. Lung tissues were processed for histological or molecular/protein analysis to determine (1) number of proliferating cells by BrdU and phospho-Histone H3 staining and (2) gene and protein expression of cell cycle regulatory proteins by real-time PCR and Western blotting. Results: After 24 h of ventilation arterial blood gas values were within normal range but alveolar formation was reduced. The number of proliferating cells was decreased (BrdU incorporation decreased from 10 to 3 % and phospho-histone H3 positive cells from 0.8 to 0.1%. Expression of CyclinD1 and E1 mRNA and protein was markedly down-regulated. Instead, protein expression of the CDK inhibitor p27Kip1 was significantly increased while its phosphorylation at site T157, T198 and T187 was decreased. Interestingly, CDK inhibitor p16Ink4a levels were decreased by ventilation. Conclusions: Prolonged mechanical ventilation causes cycle arrest of lung cells in newborn rats by increased transcription and nuclear localization of the CDK inhibitor p27Kip1. These data may in part explain the arrest in alveolarization by mechanical ventilation of the neonatal lung. ARTICLE PDF AUTHOR INFORMATION AUTHORS AND AFFILIATIONS * Pediatrics, Erasmus MC - Sophia Children's Hospital, Rotterdam, The Netherlands A A Kroon * Lung Biology Research, Physiology and Experimental Medicine Program, Hospital for Sick Children, Toronto, ON, Canada A A Kroon, J Wang, Z Huang, M Kuliszewski & M Post Authors * A A Kroon View author publications You can also search for this author inPubMed Google Scholar * J Wang View author publications You can also search for this author inPubMed Google Scholar * Z Huang View author publications You can also search for this author inPubMed Google Scholar * M Kuliszewski View author publications You can also search for this author inPubMed Google Scholar * M Post View author publications You can also search for this author inPubMed Google Scholar RIGHTS AND PERMISSIONS Reprints and permissions ABOUT THIS ARTICLE CITE THIS ARTICLE Kroon, A., Wang, J., Huang, Z. _et al._ 84 Prolonged Ventilation Causes P27KIP1 Induced Cell Cycle Arrest in Newborn Rat Lung. _Pediatr Res_ 68 (Suppl 1), 45 (2010). https://doi.org/10.1203/00006450-201011001-00084 Download citation * Issue Date: November 2010 * DOI: https://doi.org/10.1203/00006450-201011001-00084 SHARE THIS ARTICLE Anyone you share the following link with will be able to read this content: Get shareable link Sorry, a shareable link is not currently available for this article. Copy to clipboard Provided by the Springer Nature SharedIt content-sharing initiative

ABSTRACT Background: I_n vitro_ studies have demonstrated that mechanical stretch can inhibit lung cell proliferation. This inhibition of cell growth may lead to reduction of alveolar


formation and contribute to the development of bronchopulmonary dyplasia. Objective: To determine the effect of prolonged mechanical ventilation on cell-cycle regulation in a newborn rat


model. Methods: 7-day old Wistar rats were ventilated with low/moderate tidal volume and room air for 24 h. Following ventilation arterial blood gas analysis was performed and the animal was


killed. Lung tissues were processed for histological or molecular/protein analysis to determine (1) number of proliferating cells by BrdU and phospho-Histone H3 staining and (2) gene and


protein expression of cell cycle regulatory proteins by real-time PCR and Western blotting. Results: After 24 h of ventilation arterial blood gas values were within normal range but alveolar


formation was reduced. The number of proliferating cells was decreased (BrdU incorporation decreased from 10 to 3 % and phospho-histone H3 positive cells from 0.8 to 0.1%. Expression of


CyclinD1 and E1 mRNA and protein was markedly down-regulated. Instead, protein expression of the CDK inhibitor p27Kip1 was significantly increased while its phosphorylation at site T157,


T198 and T187 was decreased. Interestingly, CDK inhibitor p16Ink4a levels were decreased by ventilation. Conclusions: Prolonged mechanical ventilation causes cycle arrest of lung cells in


newborn rats by increased transcription and nuclear localization of the CDK inhibitor p27Kip1. These data may in part explain the arrest in alveolarization by mechanical ventilation of the


neonatal lung. ARTICLE PDF AUTHOR INFORMATION AUTHORS AND AFFILIATIONS * Pediatrics, Erasmus MC - Sophia Children's Hospital, Rotterdam, The Netherlands A A Kroon * Lung Biology


Research, Physiology and Experimental Medicine Program, Hospital for Sick Children, Toronto, ON, Canada A A Kroon, J Wang, Z Huang, M Kuliszewski & M Post Authors * A A Kroon View author


publications You can also search for this author inPubMed Google Scholar * J Wang View author publications You can also search for this author inPubMed Google Scholar * Z Huang View author


publications You can also search for this author inPubMed Google Scholar * M Kuliszewski View author publications You can also search for this author inPubMed Google Scholar * M Post View


author publications You can also search for this author inPubMed Google Scholar RIGHTS AND PERMISSIONS Reprints and permissions ABOUT THIS ARTICLE CITE THIS ARTICLE Kroon, A., Wang, J.,


Huang, Z. _et al._ 84 Prolonged Ventilation Causes P27KIP1 Induced Cell Cycle Arrest in Newborn Rat Lung. _Pediatr Res_ 68 (Suppl 1), 45 (2010).


https://doi.org/10.1203/00006450-201011001-00084 Download citation * Issue Date: November 2010 * DOI: https://doi.org/10.1203/00006450-201011001-00084 SHARE THIS ARTICLE Anyone you share the


following link with will be able to read this content: Get shareable link Sorry, a shareable link is not currently available for this article. Copy to clipboard Provided by the Springer


Nature SharedIt content-sharing initiative