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Biphasic Response of Protein Kinase A to Cyclic Adenosine Monophosphate Triggers Distinct Epithelial Phenotypes

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Culturing MDCK Cells in Three Dimensions for Analyzing Intracellular Dynamics

inferredcites →https://doi.org/10.1002/bies.20839openalex-snapshot

The biphasic behavior of incoherent feed‐forward loops in biomolecular regulatory networks

inferredcites →https://doi.org/10.1002/jcp.1041000210openalex-snapshot

Hemicyst formation stimulated by cyclic AMP in dog kidney cell line MDCK

inferredcites →https://doi.org/10.1007/s00239-001-0013-1openalex-snapshot

Classification and Phylogenetic Analysis of the cAMP-Dependent Protein Kinase Regulatory Subunit Family

inferredcites →https://doi.org/10.1016/0092-8674(89)90013-5openalex-snapshot

Cyclic AMP stimulates somatostatin gene transcription by phosphorylation of CREB at serine 133

inferredcites →https://doi.org/10.1016/j.bbapap.2013.03.007openalex-snapshot

PKA: Lessons learned after twenty years

inferredcites →https://doi.org/10.1016/j.cellsig.2008.02.022openalex-snapshot

Relations between the mitogen-activated protein kinase and the cAMP-dependent protein kinase pathways: Comradeship and hostility

inferredcites →https://doi.org/10.1016/j.molcel.2013.01.004openalex-snapshot

The Utility of Paradoxical Components in Biological Circuits

inferredcites →https://doi.org/10.1016/j.ydbio.2009.09.024openalex-snapshot

Morphogenesis of epithelial tubes: Insights into tube formation, elongation, and elaboration

inferredcites →https://doi.org/10.1016/s0021-9258(19)34204-8openalex-snapshot

An Adenosine 3′,5′-Monophosphate-dependant Protein Kinase from Rabbit Skeletal Muscle

inferredcites →https://doi.org/10.1016/s0962-8924(02)02294-8openalex-snapshot

Crosstalk between cAMP and MAP kinase signaling in the regulation of cell proliferation

inferredcites →https://doi.org/10.1021/cr000236lopenalex-snapshot

Physiological Substrates of cAMP-Dependent Protein Kinase

inferredcites →https://doi.org/10.1038/msb.2008.43openalex-snapshot

The incoherent feed‐forward loop can generate non‐monotonic input functions for genes

inferredcites →https://doi.org/10.1038/ncb3164openalex-snapshot

Inactivation of a Gαs–PKA tumour suppressor pathway in skin stem cells initiates basal-cell carcinogenesis

inferredcites →https://doi.org/10.1038/nchembio.1589openalex-snapshot

Endosomal GPCR signaling turned off by negative feedback actions of PKA and v-ATPase

inferredcites →https://doi.org/10.1038/nchembio.1665openalex-snapshot

Spatial encoding of cyclic AMP signaling specificity by GPCR endocytosis

inferredcites →https://doi.org/10.1038/ncomms1605openalex-snapshot

PKA regulatory subunits mediate synergy among conserved G-protein-coupled receptor cascades

inferredcites →https://doi.org/10.1038/nrm911openalex-snapshot

Cyclic nucleotide research — still expanding after half a century

inferredcites →https://doi.org/10.1046/j.1523-1755.2000.00991.xopenalex-snapshot

cAMP stimulates the in vitro proliferation of renal cyst epithelial cells by activating the extracellular signal-regulated kinase pathway

inferredcites →https://doi.org/10.1073/pnas.1709123114openalex-snapshot

Systems-level identification of PKA-dependent signaling in epithelial cells

inferredcites →https://doi.org/10.1073/pnas.86.15.6007openalex-snapshot

Renal epithelial cyst formation and enlargement in vitro: dependence on cAMP.

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Molecular cloning, characterization, and localization of a high-affinity serotonin receptor (5-HT7) activating cAMP formation.

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GABP Mediates Insulin-increased Prolactin Gene Transcription

inferredcites →https://doi.org/10.1074/jbc.271.28.16526openalex-snapshot

Phosphorylation and Activation of a cAMP-specific Phosphodiesterase by the cAMP-dependent Protein Kinase

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Analysis of the Gs/Mitogen-activated Protein Kinase Pathway in Mutant S49 Cells

inferredcites →https://doi.org/10.1074/jbc.m106457200openalex-snapshot

β-Arrestin Scaffolding of the ERK Cascade Enhances Cytosolic ERK Activity but Inhibits ERK-mediated Transcription following Angiotensin AT1a Receptor Stimulation

inferredcites →https://doi.org/10.1074/jbc.m110.185496openalex-snapshot

Light Modulation of Cellular cAMP by a Small Bacterial Photoactivated Adenylyl Cyclase, bPAC, of the Soil Bacterium Beggiatoa

inferredcites →https://doi.org/10.1074/jbc.m116.768986openalex-snapshot

Phosphorylation of Rap1 by cAMP-dependent Protein Kinase (PKA) Creates a Binding Site for KSR to Sustain ERK Activation by cAMP

inferredcites →https://doi.org/10.1074/jbc.m404101200openalex-snapshot

The Functional Consequences of Cross-talk between the Vitamin D Receptor and ERK Signaling Pathways Are Cell-specific

inferredcites →https://doi.org/10.1074/jbc.m707009200openalex-snapshot

β2-Adrenergic Receptor Signaling and Desensitization Elucidated by Quantitative Modeling of Real Time cAMP Dynamics

inferredcites →https://doi.org/10.1074/jbc.m801313200openalex-snapshot

A Novel Protein Kinase A-independent, β-Arrestin-1-dependent Signaling Pathway for p38 Mitogen-activated Protein Kinase Activation by β2-Adrenergic Receptors

inferredcites →https://doi.org/10.1074/jbc.m802476200openalex-snapshot

Biphasic Regulation of Mammary Epithelial Resistance by Serotonin through Activation of Multiple Pathways

inferredcites →https://doi.org/10.1083/jcb.148.6.1267openalex-snapshot

β-Arrestin–Dependent Endocytosis of Proteinase-Activated Receptor 2 Is Required for Intracellular Targeting of Activated Erk1/2

inferredcites →https://doi.org/10.1091/mbc.e12-02-0078openalex-snapshot

Cyclic AMP regulates formation of mammary epithelial acini in vitro

inferredcites →https://doi.org/10.1091/mbc.e16-06-0354openalex-snapshot

Model-guided optogenetic study of PKA signaling in budding yeast

inferredcites →https://doi.org/10.1093/nar/gkm415openalex-snapshot

DAVID Bioinformatics Resources: expanded annotation database and novel algorithms to better extract biology from large gene lists

inferredcites →https://doi.org/10.1093/nar/gkw377openalex-snapshot

Enrichr: a comprehensive gene set enrichment analysis web server 2016 update

inferredcites →https://doi.org/10.1096/fj.201601116ropenalex-snapshot

Critical role of the cAMP‐PKA pathway in hyperglycemia‐induced epigenetic activation of fibrogenic program in the kidney

inferredcites →https://doi.org/10.1101/cshperspect.a011148openalex-snapshot

The Cyclic AMP Pathway

inferredcites →https://doi.org/10.1101/lm.1231009openalex-snapshot

Exchange protein activated by cAMP enhances long-term memory formation independent of protein kinase A

inferredcites →https://doi.org/10.1111/j.1749-6632.1981.tb15490.xopenalex-snapshot

MORPHOLOGICAL SIMILARITIES BETWEEN THE DOG KIDNEY CELL LINE MDCK AND THE MAMMALIAN CORTICAL COLLECTING TUBULE*

inferredcites →https://doi.org/10.1126/science.aaj1669openalex-snapshot

Local protein kinase A action proceeds through intact holoenzymes

inferredcites →https://doi.org/10.1126/scisignal.122re4openalex-snapshot

Pharmacological PKA Inhibition: All May Not Be What It Seems

inferredcites →https://doi.org/10.1126/scisignal.2004621openalex-snapshot

Interconnected Network Motifs Control Podocyte Morphology and Kidney Function

inferredcites →https://doi.org/10.1146/annurev.bi.59.070190.004543openalex-snapshot

cAMP-DEPENDENT PROTEIN KINASE: FRAMEWORK FOR A DIVERSE FAMILY OF REGULATORY ENZYMES

inferredcites →https://doi.org/10.1152/ajpcell.00084.2009openalex-snapshot

Inhibition of basal p38 or JNK activity enhances epithelial barrier function through differential modulation of claudin expression

inferredcites →https://doi.org/10.1177/153537020623100308openalex-snapshot

Lixazinone Stimulates Mitogenesis of Madin-Darby Canine Kidney Cells

inferredcites →https://doi.org/10.1186/1471-2121-12-43openalex-snapshot

The MDCK variety pack: choosing the right strain

inferredcites →https://doi.org/10.1186/s12859-017-1934-zopenalex-snapshot

ImageJ2: ImageJ for the next generation of scientific image data

inferredcites →https://doi.org/10.1186/s13059-014-0550-8openalex-snapshot

Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2

inferredcites →https://doi.org/10.1196/annals.1378.076openalex-snapshot

c‐Jun and JunB Are Essential for Hypoglycemia‐Mediated VEGF Induction

inferredcites →https://doi.org/10.1242/dev.127944openalex-snapshot

Mammary epithelial tubes elongate through MAPK-dependent coordination of cell migration

inferredcites →https://doi.org/10.1242/dev.128.21.4329openalex-snapshot

Erk MAP kinase regulates branching morphogenesis in the developing mouse kidney

inferredcites →https://doi.org/10.1242/jcs.114140openalex-snapshot

Separate roles of PKA and EPAC in renal function unraveled by the optogenetic control of cAMP levels in vivo

inferredcites →https://doi.org/10.1371/journal.pone.0021800openalex-snapshot

REVIGO Summarizes and Visualizes Long Lists of Gene Ontology Terms

inferredcites →https://doi.org/10.2741/skalheggopenalex-snapshot

Specificity in the cAMP/PKA signaling pathway. differential expression, regulation, and subcellular localization of subunits of PKA

inferredcites →https://doi.org/10.7554/elife.05161openalex-snapshot

Controlling fertilization and cAMP signaling in sperm by optogenetics

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1371/journal.pcbi.1009873openalex-snapshot

Analysis of localized cAMP perturbations within a tissue reveal the effects of a local, dynamic gap junction state on ERK signaling

inferred← citeshttps://doi.org/10.7554/elife.86520openalex-snapshot

A unified approach to dissecting biphasic responses in cell signaling

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