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Aberrant Ca2+ handling in lysosomal storage disorders

期刊

CELL CALCIUM
卷 47, 期 2, 页码 103-111

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.ceca.2009.12.007

关键词

Lysosomal storage diseases; Calcium; Autophagy; Mitochondria; Signaling; Lysosomes; Ion channels; Mucolipins; Two pore channels; TRPML1; TRPML3; Cell death

资金

  1. National Institutes of Health [HD058577, ES016782, DE12309, DK38938]
  2. Ruth S. Harrell Professorship in Medical Research
  3. Uehara Memorial Foundation, Tokyo, Japan

向作者/读者索取更多资源

Lysosomal storage diseases (LSDs) are caused by inability of cells to process the material captured during endocytosis. While they are essentially diseases of cellular indigestion, LSDs affect large number of cellular activities and, as such, they teach us about the integrative function of the cell, as well as about the gaps ill our knowledge of the endocytic pathway and membrane transport. The present review summarizes recent findings on Ca2+ handling in LSDs and attempts to identify the key questions on alterations in Ca2+ signaling and membrane transport in this group of diseases, answers to which may lie in delineating the cellular pathogeneses of LSDs. (C) 2009 Elsevier Ltd. All rights reserved.

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