The annexinopathies: a new category of diseases
The annexins are a family of highly homologous phospholipid binding proteins, which share a four-domain structure, with one member of the family – annexin VI – having a duplication consisting of eight domains. Thus far, ten annexins have been described in mammals. Although the biological functions o...
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Published in | BBA - Molecular Cell Research Vol. 1498; no. 2; pp. 169 - 173 |
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Main Author | |
Format | Book Review Journal Article |
Language | English |
Published |
Netherlands
Elsevier B.V
20.12.2000
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Subjects | |
Online Access | Get full text |
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Summary: | The annexins are a family of highly homologous phospholipid binding proteins, which share a four-domain structure, with one member of the family – annexin VI – having a duplication consisting of eight domains. Thus far, ten annexins have been described in mammals. Although the biological functions of the annexins have not been definitively established, two human diseases involving annexin abnormalities (‘annexinopathies’) have been identified as of the time of writing. Overexpression of annexin II occurs in the leukocytes of a subset of patients having a hemorrhagic form of acute promyelocytic leukemia. Underexpression of annexin V occurs on placental trophoblasts in the antiphospholipid syndrome and in preeclampsia. Also, an animal model has been described in which annexin VII is underexpressed and is associated with disease, but the relevance of this animal model to human disease is not yet understood. Future research is likely to elucidate additional ‘annexinopathies’. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-3 content type line 23 ObjectType-Review-1 |
ISSN: | 0167-4889 0006-3002 1879-2596 |
DOI: | 10.1016/S0167-4889(00)00093-8 |