The diabetes-linked transcription factor Pax4 is expressed in human pancreatic islets and is activated by mitogens and GLP-1

Autor: Marc Y. Donath, Anne Wojtusciszyn, Bernhard O. Boehm, Kai Hui Hu He, Kathrin Maedler, Piero Marchetti, Nadine S. Sauter, Roberto Lupi, Benoit R. Gauthier, Thierry Brun
Přispěvatelé: University of Zurich, Gauthier, B R
Jazyk: angličtina
Rok vydání: 2017
Předmět:
Epigenesis Genetic
Interleukin-1beta
Gene Expression
Glucagon-Like Peptide 1/pharmacology
Epigenesis
Genetic

Cell Proliferation/drug effects
Islets of Langerhans/drug effects/metabolism/secretion
Diabetes Mellitus Type 2/complications/genetics/metabolism
Glucagon-Like Peptide 1
Insulin-Secreting Cells
Gene expression
Insulin Secretion
Insulin
Paired Box Transcription Factors
Homeodomain Proteins/genetics/metabolism
Genetics (clinical)
geography.geographical_feature_category
Mitogens/pharmacology
General Medicine
Cell cycle
Islet
Glucose/pharmacology
Activins
medicine.anatomical_structure
Intercellular Signaling Peptides and Proteins
Signal transduction
Interleukin-1beta/genetics
Signal Transduction
medicine.medical_specialty
2716 Genetics (clinical)
endocrine system
Insulin-Secreting Cells/cytology/drug effects/metabolism/secretion
Incretin
610 Medicine & health
Biology
Obesity/complications/genetics/metabolism
In Vitro Techniques
Transfection
142-005 142-005
Islets of Langerhans
1311 Genetics
Internal medicine
Genetics
medicine
1312 Molecular Biology
Animals
Humans
Intercellular Signaling Peptides and Proteins/pharmacology
Obesity
RNA
Messenger

fas Receptor
Betacellulin
ddc:612
Molecular Biology
Cell Proliferation
Insulin/secretion
Homeodomain Proteins
geography
Pancreatic islets
Antigens CD95/genetics
Activins/pharmacology
Rats
Paired Box Transcription Factors/genetics/metabolism
Endocrinology
Glucose
Diabetes Mellitus
Type 2

RNA Messenger/genetics/metabolism
PAX4
570 Life sciences
biology
Mitogens
Zdroj: BASE-Bielefeld Academic Search Engine
Human molecular genetics, Vol. 17, No 4 (2008) pp. 478-89
ISSN: 1460-2083
Popis: We previously demonstrated that the transcription factor Pax4 is important for beta-cell replication and survival in rat islets. Herein, we investigate Pax4 expression in islets of non-diabetic and diabetic donors, its regulation by mitogens, glucose and the incretin GLP-1 and evaluate its effect on human islet proliferation. Pax4 expression was increased in islets derived from Type 2 diabetic donors correlating with hyperglycaemia. In vitro studies on non diabetic islets demonstrated that glucose, betacellulin, activin A, GLP-1 and insulin increased Pax4 mRNA levels. Glucose-induced Pax4 expression was abolished by the inhibitors LY294002, PD98050 or H89. Surprisingly, increases in Pax4 expression did not prompt a surge in human islet cell replication. Furthermore, expression of the proliferation marker gene Id2 remained unaltered. Adenoviral-mediated expression of human Pax4 resulted in a small increase in Bcl-xL expression while Id2 transcript levels and cell replication were unchanged in human islets. In contrast, overexpression of mouse Pax4 induced human islet cell proliferation. Treatment of islets with 5-Aza-2'-deoxycytidine induced Pax4 without stimulating Bcl-xL and Id2 expression. Human Pax4 DNA binding activity was found to be lower than that of the mouse homologue. Thus, human pax4 gene expression is epigenetically regulated and induced by physiological stimuli through the concerted action of multiple signalling pathways. However, it is unable to initiate the transcriptional replication program likely due to post-translational modifications of the protein. The latter highlights fundamental differences between human and rodent islet physiology and emphasizes the importance of validating results obtained with animal models in human tissues.
Databáze: OpenAIRE