Journal Article

Alterations in the Cell Cycle in the Cerebellum of Hyperbilirubinemic Gunn Rat: A Possible Link with Apoptosis?

Furlan, Giulia, Gambaro, Sabrina Eliana, Apitsionak, Faina, Gazzin, Silvia, Robert, María Celeste, Vianello, Eleonora, Tiribelli, Claudio, Rosso, Natalia

2013

Overview

Severe hyperbilirubinemia causes neurological damage both in humans and rodents. The hyperbilirubinemic Gunn rat shows a marked cerebellar hypoplasia. More recently bilirubin ability to arrest the cell cycle progression in vascular smooth muscle, tumour cells, and, more importantly, cultured neurons has been demonstrated. However, the involvement of cell cycle perturbation in the development of cerebellar hypoplasia was never investigated before. We explored the effect of sustained spontaneous hyperbilirubinemia on cell cycle progression and apoptosis in whole cerebella dissected from 9 day old Gunn rat by Real Time PCR, Western blot and FACS analysis. The cerebellum of the hyperbilirubinemic Gunn rats exhibits an increased cell cycle arrest in the late G0/G1 phase (p < 0.001), characterized by a decrease in the protein expression of cyclin D1 (15%, p < 0.05), cyclin A/A1 (20 and 30%, p < 0.05 and 0.01, respectively) and cyclin dependent kinases2 (25%, p < 0.001). This was associated with a marked increase in the 18 kDa fragment of cyclin E (67%, p < 0.001) which amplifies the apoptotic pathway. In line with this was the increase of the cleaved form of Poly (ADP-ribose) polymerase (54%, p < 0.01) and active Caspase3 (two fold, p < 0.01). These data indicate that the characteristic cerebellar alteration in this developing brain structure of the hyperbilirubinemic Gunn rat may be partly due to cell cycle perturbation and apoptosis related to the high bilirubin concentration in cerebellar tissue mainly affecting granular cells. These two phenomena might be intimately connected.

• Publisher: Public Library of Science,Public Library of Science (PLoS)
• Subject: Adenosine diphosphate / Animals / Apoptosis / Astrocytes - cytology / Astrocytes - drug effects / Astrocytes - metabolism / Bilirubin / Bilirubin - blood / Bilirubin - metabolism / Bilirubin - pharmacology / Blotting, Western / Brain / Caspase 3 - metabolism / Cell cycle / Cell Cycle Checkpoints / Cells, Cultured / Cerebellum / Cerebellum - cytology / Cerebellum - metabolism / Cholesterol / Cyclin A / Cyclin A - genetics / Cyclin A - metabolism / Cyclin A1 - genetics / Cyclin A1 - metabolism / Cyclin D1 / Cyclin D1 - genetics / Cyclin D1 - metabolism / Cyclin E / Cyclin E - genetics / Cyclin E - metabolism / Female / Flow Cytometry / G1 Phase / Genetic aspects / Hyperbilirubinemia / Hyperbilirubinemia - blood / Hyperbilirubinemia - genetics / Hyperbilirubinemia - metabolism / Hypoplasia / Kinases / Male / Muscles / Mutation / Physiological aspects / Poly(ADP-ribose) Polymerases - metabolism / Rats / Rats, Gunn / Rats, Wistar / Resting Phase, Cell Cycle / Reverse Transcriptase Polymerase Chain Reaction / Ribose / Rodents / Smooth muscle / Tumors