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Conference Paper: Secretin protects from apoptosis by activation of ERK1/2 and CREB
Title | Secretin protects from apoptosis by activation of ERK1/2 and CREB |
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Authors | |
Issue Date | 2017 |
Publisher | BioScientifica Ltd. The Journal's web site is located at http://www.endocrine-abstracts.org/default.htm |
Citation | 19th European Congress of Endocrinology (ECE 2017), Lisbon, Portugal, 20-23 May 2017. In Endocrine Abstracts, 2017, v. 49, no. EP916 How to Cite? |
Abstract | There are a growing number of studies identifying secretin as a neuroprotective factor. Consistently, our previous data showed that neuronal apoptosis considerably increased in the developing cerebellum from secretin knockout (Sct-/-) mice. However, the underlying mechanisms remained poorly understood. Extracellular signal-regulated protein kinase (ERK) and AKT signalling pathways are known for the regulation of apoptosis. Additionally, these two pathways could activate cAMP-response-element-binding protein (CREB), which has been shown to promote cell survival. Therefore, their phosphorylation levels in the cerebellum were compared between Sct-/- and WT mice. The basal levels of phosphor-ERK1/2 (pERK1/2) and phosphor-CREB (pCREB) showed a significant decrease in Sct-/- mice, but not phosphor-AKT (pAKT). The cerebellar slices obtained from Sct-/- displayed a dose-dependent increase of pERK1/2 and pCREB, but not pAKT, in response to graded concentrations of secretin peptide and the impaired phosphorylation of ERK1/2 and CREB in Sct-/- cerebellar slices was able to be recovered by the treatment of secretin compared with WT, suggesting the involvement of ERK1/2 and CREB. Specific inhibitors were applied for further confirmation. Secretin failed to reduce the level of activated Caspase-3 when either ERK1/2 or CREB was inhibited, revealing that ERK1/2 and CREB was required for secretin’s neuroprotective function. Our results clearly provide evidence that ERK1/2 and CREB play a role in mediating the anti-apoptotic function of secretin. |
Persistent Identifier | http://hdl.handle.net/10722/262106 |
ISSN |
DC Field | Value | Language |
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dc.contributor.author | Wang, L | - |
dc.contributor.author | Chow, BKC | - |
dc.date.accessioned | 2018-09-28T04:53:25Z | - |
dc.date.available | 2018-09-28T04:53:25Z | - |
dc.date.issued | 2017 | - |
dc.identifier.citation | 19th European Congress of Endocrinology (ECE 2017), Lisbon, Portugal, 20-23 May 2017. In Endocrine Abstracts, 2017, v. 49, no. EP916 | - |
dc.identifier.issn | 1470-3947 | - |
dc.identifier.uri | http://hdl.handle.net/10722/262106 | - |
dc.description.abstract | There are a growing number of studies identifying secretin as a neuroprotective factor. Consistently, our previous data showed that neuronal apoptosis considerably increased in the developing cerebellum from secretin knockout (Sct-/-) mice. However, the underlying mechanisms remained poorly understood. Extracellular signal-regulated protein kinase (ERK) and AKT signalling pathways are known for the regulation of apoptosis. Additionally, these two pathways could activate cAMP-response-element-binding protein (CREB), which has been shown to promote cell survival. Therefore, their phosphorylation levels in the cerebellum were compared between Sct-/- and WT mice. The basal levels of phosphor-ERK1/2 (pERK1/2) and phosphor-CREB (pCREB) showed a significant decrease in Sct-/- mice, but not phosphor-AKT (pAKT). The cerebellar slices obtained from Sct-/- displayed a dose-dependent increase of pERK1/2 and pCREB, but not pAKT, in response to graded concentrations of secretin peptide and the impaired phosphorylation of ERK1/2 and CREB in Sct-/- cerebellar slices was able to be recovered by the treatment of secretin compared with WT, suggesting the involvement of ERK1/2 and CREB. Specific inhibitors were applied for further confirmation. Secretin failed to reduce the level of activated Caspase-3 when either ERK1/2 or CREB was inhibited, revealing that ERK1/2 and CREB was required for secretin’s neuroprotective function. Our results clearly provide evidence that ERK1/2 and CREB play a role in mediating the anti-apoptotic function of secretin. | - |
dc.language | eng | - |
dc.publisher | BioScientifica Ltd. The Journal's web site is located at http://www.endocrine-abstracts.org/default.htm | - |
dc.relation.ispartof | Endocrine Abstracts | - |
dc.relation.ispartof | 19th European Congress of Endocrinology (ECE 2017) | - |
dc.title | Secretin protects from apoptosis by activation of ERK1/2 and CREB | - |
dc.type | Conference_Paper | - |
dc.identifier.email | Chow, BKC: bkcc@hku.hk | - |
dc.identifier.authority | Chow, BKC=rp00681 | - |
dc.identifier.doi | 10.1530/endoabs.49.EP916 | - |
dc.identifier.hkuros | 292921 | - |
dc.identifier.volume | 49 | - |
dc.identifier.spage | EP916 | - |
dc.identifier.epage | EP916 | - |
dc.publisher.place | United Kingdom | - |
dc.identifier.issnl | 1470-3947 | - |