Deficits in spatial learning and motor coordination in ADAM11-deficient mice
By E. Takahashi, K. Sagane, T. Oki, K. Yamazaki, T. Nagasu, J. Kuromitsu. 2006
47 citations recorded by the source corpus.
BackgroundADAM11 is a member of the ADAM gene family and is mainly expressed in the nervous system. It is thought to be an adhesion molecule, since it has a disintegrin-like domain related to cell-cell or cell-matrix interactions. To elucidate the physiological functions of ADAM11, we generated ADAM11-deficient mice by means of gene targeting.ResultsADAM11-deficient mice were apparently normal, and survived more than one year with no major histological abnormalities in the brain or spinal cord. Because ADAM11 is highly expressed in the hippocampus and cerebellum, we have examined ADAM11 mutant mice for learning using visual and hidden water maze tasks, and their motor coordination using a rotating rod task. Our results showed that their visual water maze task results are normal, but the hidden water maze and rotating rod task skills are impaired in ADAM11-deficient mice.ConclusionOur results indicate that ADAM11 mutation does not affect cell migration and differentiation during development, but affects learning and motor coordination. Thus, ADAM11 might play an important signalling or structural role as a cell adhesion molecule at the synapse, and may thus participate in synaptic regulation underlying behavioural changes.
Subfields: Cellular and Molecular Neuroscience, Molecular Biology, Oncology
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Molecular Biology
- M. Handsley
- Carlos Fernandez-Patron
- D. Edwards
- S. Zhong
- Pu Zhang
- R. Khalil
- Mengcheng Shen
- C. Pennington
In Oncology
- S. Zhong
- M. Handsley
- Carlos Fernandez-Patron
- D. Edwards
- Pu Zhang
- R. Khalil
- Mengcheng Shen
- C. Pennington
Citations in the corpus
- A Disintegrin and Metalloproteinase (ADAM) and ADAM with Thrombospondin Motifs (ADAMTS) Family in Vascular Biology and Disease (2019, background): “ADAM-11−/− mice have a normal development phenotype, but suffer from learning deficiency [69].”
- ADAMs family and relatives in cardiovascular physiology and pathology. (2016, background): “[129]”
- The ADAM metalloproteinases (2008, background): “Though Adam11À/À mice are apparently normal, these mice show defects in learning in the water maze task and motor coordination in the rotating rod task (Takahashi et al., 2006a) .”