Literature DB >> 36237516

Morphological Alterations of CAD Cells Overexpressing AKT1.

James Wachira1.   

Abstract

CAD cells are neuronal cells used in studies of cell differentiation and in cellular models of neuropathology. When cultured in differentiation medium, CAD cells exhibit characteristics of mature neurons including the generation of action potential. In addition to being a central signaling kinase in cell survival, AKT1 plays important roles in the nervous system including neuroplasticity and this study examined the localization of exogenous AKT1 in CAD cells. Neuropeptides modulate many signal transduction pathways and melacortins are implicated in regulating growth factor signal transduction pathways, including the PI3K/AKT pathway. AKT1-DsReD was transfected into CAD cells that were stably expressing melanocortin 3-receptor-GFP (MC3R-GFP), a G-protein coupled receptor. The cells were imaged with confocal microscopy to determine the fluorescent protein localization patterns. AKT1-DsRed was predominantly localized in the cytoplasm and the nucleus. Further, expression of exogenous AKT1 in these cell lines led to morphological changes reminiscent of apoptosis. As expected, MC3R-GFP localized to the plasma membrane but it internalized upon cell stimulation with the cognate ligand. In limited areas of the plasma membrane, AKT1-DsRed and MC3R-GFP were colocalized. In conclusion, quantitative studies to understand the role of relative levels of AKT1 in determining cell survival are needed.

Entities:  

Year:  2020        PMID: 36237516      PMCID: PMC9555227          DOI: 10.1017/s1431927620017821

Source DB:  PubMed          Journal:  Microsc Microanal        ISSN: 1431-9276            Impact factor:   4.099


  8 in total

1.  The natural inverse agonist agouti-related protein induces arrestin-mediated endocytosis of melanocortin-3 and -4 receptors.

Authors:  Andreas Breit; Katharina Wolff; Hermann Kalwa; Hubertus Jarry; Thomas Büch; Thomas Gudermann
Journal:  J Biol Chem       Date:  2006-10-14       Impact factor: 5.157

2.  Immunohistochemical characterisation of differentiated CAD cells: expression of peptides and chromogranins.

Authors:  Yongling Li; Linda Xiu-E Hou; Annika Aktiv; Annica Dahlström
Journal:  Histochem Cell Biol       Date:  2005-07-09       Impact factor: 4.304

Review 3.  G Protein-Coupled Receptor Signaling Through β-Arrestin-Dependent Mechanisms.

Authors:  Pierre-Yves Jean-Charles; Suneet Kaur; Sudha K Shenoy
Journal:  J Cardiovasc Pharmacol       Date:  2017-09       Impact factor: 3.105

4.  Changes in cellular prion protein expression, processing and localisation during differentiation of the neuronal cell line CAD 5.

Authors:  Zuzana Fremuntova; Tibor Mosko; Jakub Soukup; Johanka Kucerova; Marie Kostelanska; Zdenka Backovska Hanusova; Marcela Filipova; Larisa Cervenakova; Karel Holada
Journal:  Biol Cell       Date:  2019-12-06       Impact factor: 4.458

Review 5.  Biased signaling at neural melanocortin receptors in regulation of energy homeostasis.

Authors:  Li-Kun Yang; Ya-Xiong Tao
Journal:  Biochim Biophys Acta Mol Basis Dis       Date:  2017-04-19       Impact factor: 5.187

6.  Endosomal colocalization of melanocortin-3 receptor and beta-arrestins in CAD cells with altered modification of AKT/PKB.

Authors:  D C Nyan; R Anbazhagan; C A Hughes-Darden; S J M Wachira
Journal:  Neuropeptides       Date:  2008-03-04       Impact factor: 3.286

7.  All-trans-retinoid acid induces the differentiation of P19 cells into neurons involved in the PI3K/Akt/GSK3β signaling pathway.

Authors:  Fang Fu; Lu-Shan Li; Ru Li; Qiong Deng; Qiu-Xia Yu; Xin Yang; Min Pan; Jin Han; Li Zhen; Li-Na Zhang; Ting-Ying Lei; Dong-Zhi Li; Can Liao
Journal:  J Cell Biochem       Date:  2020-01-21       Impact factor: 4.429

Review 8.  Akt signalling in health and disease.

Authors:  Ingeborg Hers; Emma E Vincent; Jeremy M Tavaré
Journal:  Cell Signal       Date:  2011-05-17       Impact factor: 4.315

  8 in total

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