Improvement of multiple pathophysiological phenotypes ofklotho (kl/kl) mice by adenovirus-mediated expression of theklotho gene
| Autor: | Masaki Noda, Yo-ichi Nabeshima, Akihiro Iida, Takako Shiraki-Iida, Satoshi Nishikawa, Makoto Kuro-o, Hideharu Anazawa, Yoko Nabeshima |
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| Rok vydání: | 2000 |
| Předmět: |
Premature aging
medicine.medical_specialty Mutation Transgene Chinese hamster ovary cell Biology urologic and male genital diseases medicine.disease_cause female genital diseases and pregnancy complications Viral vector Adenoviridae Endocrinology Cell culture Internal medicine Drug Discovery Genetics medicine Cancer research Molecular Medicine Molecular Biology Klotho Genetics (clinical) |
| Zdroj: | The Journal of Gene Medicine. 2:233-242 |
| ISSN: | 1521-2254 1099-498X |
| DOI: | 10.1002/1521-2254(200007/08)2:4<233::aid-jgm110>3.0.co;2-5 |
| Popis: | Background We have established a novel mouse mutant, klotho (kl), by insertional mutation of a transgene and identified the structural gene. The mouse homozygous for the mutation exhibits multiple pathological conditions resembling age-related disorders in humans and can be regarded as a model of human premature aging syndromes. However, the pathophysiological role of Klotho protein has not been clarified. Methods A replication-deficient adenoviral vector expressing the membrane form of the mouse klotho gene was constructed and we examined Klotho expression in vitro. The recombinant adenoviral vector was then administered intravenously into klotho mice at 4–5 weeks of age and its therapeutic potential was examined. Results Expression of Klotho protein was observed in the adenoviral vector-infected CHO cells. The klotho mice infused with the recombinant adenovirus showed a significant extension of life span and gain in body weight at 1 week after treatment. Macroscopic and histological analyses demonstrated the improvement of multiple pathological findings such as restoration from atrophy and cell formation and differentiation in the gonadal cells, immune tissues and subcutaneous fat. Conclusion We showed that local expression of the klotho gene retards or partially improves pathological abnormalities in several organs of klotho mice after onset of the phenotypes. Therefore, the recombinant adenovirus vector will provide an important tool for investigating the molecular mechanism of the Klotho protein and give clues to understanding the individual disease mechanisms. Copyright © 2000 John Wiley & Sons, Ltd. |
| Databáze: | OpenAIRE |
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