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- Imai Yumiko
- Department of Biological Informatics and Experimental Therapeutics, the Global COE program, Akita University Graduate School of Medicine
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- Kuba Keiji
- Department of Biological Informatics and Experimental Therapeutics, the Global COE program, Akita University Graduate School of Medicine
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- Ohto-Nakanishi Takayo
- Department of Biological Informatics and Experimental Therapeutics, the Global COE program, Akita University Graduate School of Medicine
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- Penninger Josef M.
- Institute of Molecular Biotechnology of the Austrian Academy of Sciences (IMBA)
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説明
Angiotensin-converting enzyme 2 (ACE2), a first homolog of ACE, regulates the renin-angiotensin system by counterbalancing ACE activity. Accumulating evidence in recent years has demonstrated a physiological and pathological role of ACE2 in the cardiovascular, renal and respiratory systems. For instance, in the acute respiratory distress syndrome (ARDS), ACE, AngII, and AT1R promote the disease pathogenesis, whereas ACE2 and the AT2R protect from ARDS. Importantly, ACE2 has been identified as a key SARS-coronavirus receptor and plays a protective role in SARS pathogenesis. Furthermore, the recent explosion of research into the ACE2 homolog, collectrin, has revealed a new physiological function of ACE2 as an amino acid transporter, which explains the pathogenic role of gene mutations in Hartnup disorder. This review summarizes and discusses the recently unveiled roles for ACE2 in disease pathogenesis. (Circ J 2010; 74: 405 - 410)<br>
収録刊行物
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- Circulation Journal
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Circulation Journal 74 (3), 405-410, 2010
一般社団法人 日本循環器学会
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詳細情報 詳細情報について
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- CRID
- 1390282680081361280
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- NII論文ID
- 10025942941
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- NII書誌ID
- AA11591968
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- ISSN
- 13474820
- 13469843
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- 本文言語コード
- en
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- データソース種別
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- JaLC
- Crossref
- CiNii Articles
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- 抄録ライセンスフラグ
- 使用不可