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PMID:11246230

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Citation

Bajenaru, ML, Donahoe, J, Corral, T, Reilly, KM, Brophy, S, Pellicer, A and Gutmann, DH (2001) Neurofibromatosis 1 (NF1) heterozygosity results in a cell-autonomous growth advantage for astrocytes. Glia 33:314-23

Abstract

Individuals with neurofibromatosis 1 (NF1) develop low-grade astrocytomas at an increased frequency. To gain insight into the function of the Nf1 gene product as a growth regulator for astrocytes, we examined mice heterozygous for a targeted Nf1 mutation. In our previous studies, we demonstrated increased numbers of proliferating astrocytes in Nf1 heterozygote (Nf1+/-) mice in vivo. We now show that cultured Nf1+/- astrocytes exhibit a cell-autonomous growth advantage in vitro associated with increased p21-ras pathway activation. Furthermore, we demonstrate that Nf1+/-;wild-type N-ras mice have a similar astrocyte growth advantage in vitro and in vivo as either oncogenic N-ras or Nf1+/-; oncogenic N-ras mice. Lastly, mice heterozygous for targeted defects in both Nf1 and p53 as well as Nf1 and Rb exhibit 3- and 2.5-fold increases in astrocyte proliferation in vivo, respectively, suggesting that abnormalities in Nf1- and p53/Rb-regulated pathways cooperate in the heterozygous state to confer a growth advantage for brain astrocytes. Collectively, these results provide evidence for a cell-autonomous growth advantage in Nf1+/- astrocytes and suggest that some of the brain pathology in individuals with NF1 might result from reduced, but not absent, NF1 gene function.

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PubMed

Keywords

Animals; Astrocytes/cytology; Astrocytes/physiology; Astrocytoma/genetics; Brain Neoplasms/genetics; Cell Count; Cell Division/physiology; Cells, Cultured; Heterozygote; Mice; Mice, Knockout; Neocortex/cytology; Nerve Tissue Proteins/genetics; Neurofibromin 1; Proto-Oncogene Proteins p21(ras)/physiology; Retinoblastoma Protein/genetics; Tumor Suppressor Protein p53/genetics

Significance

Annotations

Gene product Qualifier GO ID GO term name Evidence Code with/from Aspect Notes Status


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References

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