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Lithium suppresses epidermal SERCA2 and PMR1 levels in the rat

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Pathology & Oncology Research

Abstract

Autosomal dominant mutations in the genes encoding the calcium ATPases SERCA2 and PMR1/SPCA1 cause the genodermatoses Darier disease (DD) and Hailey-Hailey disease (HHD), respectively. Recent observations indicated that the level of the pathogenic proteins greatly decreases in the affected areas of the epidermis in these disorders. Here we addressed how lithium, a recognized exacerbating factor in Darier disease, affects the epidermal expression of SERCA2 and PMR1/SPCA1 in the rat as a model. Standard histologic and immunohistochemical methods were utilized in 3 lithium-treated and 3 control animals. A significant suppression of epidermal SERCA2 and PMR1 levels were observed as a result of lithium therapy in addition to marked qualitative and quantitative changes in the stratum corneum and the granular layer of the epidermis in the treated animals. Our findings suggest that exacerbating factors in calcium ATPase disorders of the skin suppress epidermal SERCA2 and PMR1 levels, further decreasing the already haploinsufficient protein expression to a potentially critical level in Darier disease and Hailey-Hailey disease, respectively. Lithium therapy should specifically be avoided not only in Darier disease, but Hailey-Hailey disease as well.

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References

  1. Sakuntabhai A, Ruiz-Perez V, Carter S, et al: Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease. Nat Genet 21: 271–277, 1999

    Article  PubMed  CAS  Google Scholar 

  2. HuZ, Bonifas JM, Beech J, et al: Mutations in ATP2C1, encoding a calcium pump, cause Hailey-Hailey disease. Nat Genet 24: 61–65, 2000

    Article  Google Scholar 

  3. Tavadia S, Authi KS, Hodgins MB, Munro CS: Expression of the sarco/endoplasmic reticulum calcium ATPase type 2 and 3 isoforms in normal skin and Darier’s disease. Br J Dermatol 151: 440–445, 2004

    Article  PubMed  CAS  Google Scholar 

  4. Porgpermdee S, Yu X, Takagi A, et al: Expression of SPCA1 (Hailey-Hailey disease gene product) in acantholytic dermatoses. J Dermatol Sci 40: 137–140, 2005

    Article  PubMed  CAS  Google Scholar 

  5. Mayuzumi N, Ikeda S, Kawada H, et al: Effects of ultraviolet B irradiation, proinflammatory cytokines and raised extracellular calcium concentration on the expression of ATP2A2 and ATP2C1. Br J Dermatol 152: 697–701, 2005

    Article  PubMed  CAS  Google Scholar 

  6. Rubin MB: Lithium-induced Darier’s disease. J Am Acad Dermatol 32: 674–675, 1995

    Article  PubMed  CAS  Google Scholar 

  7. Kellermayer R: Hailey-Hailey disease as an orthodisease of PMR1 deficiency in Saccharomyces cerevisiae. FEBS Lett 579: 2021–2025, 2005

    Article  PubMed  CAS  Google Scholar 

  8. Prasad V, Boivin GP, Miller ML, et al: Haploinsufficiency of Atp2a2, encoding the sarco(endo)plasmic reticulum Ca2+-ATPase isoform 2 Ca2+ pump, predisposes mice to squamous cell tumors via a novel mode of cancer susceptibility. Cancer Res 65: 8655–8661, 2005

    Article  PubMed  CAS  Google Scholar 

  9. Burge SM, Schomberg KH: Adhesion molecules and related proteins in Darier’s disease and Hailey-Hailey disease. Br J Dermatol 127: 335–343, 1992

    Article  PubMed  CAS  Google Scholar 

  10. Elias PM, Nau P, Hartley K, et al: Formation of the epidermal calcium gradient coincides with key milestones of barrier ontogenesis in the rodent. J Invest Dermatol 110: 399–404, 1998

    Article  PubMed  CAS  Google Scholar 

  11. Green E, Elvidge G, Jacobsen N, et al: Localization of bipolar susceptibility locus by molecular genetic analysis of the chromosome 12q23–q24 region in two pedigrees with bipolar disorder and Darier’s disease. Am J Psychiatry 162: 35–42, 2005

    Article  PubMed  Google Scholar 

  12. Kellermayer R, Szigeti R, Keeling KM, et al: Aminoglycosides as potential pharmacogenetic agents in the treatment of Hailey-Hailey disease. J Invest Dermatol 126: 229–231, 2006

    Article  PubMed  CAS  Google Scholar 

  13. Yeung CK, Chan HH: Cutaneous adverse effects of lithium: epidemiology and management. Am J Clin Dermatol 5: 3–8, 2004

    Article  PubMed  Google Scholar 

  14. Csutora P, Karsai A, Nagy T, et al: Lithium induces phosphoglucomutase activity in various tissues of rats and in bipolar patients. Int J Neuropsychopharmacol 9:613–619, 2006

    Article  PubMed  CAS  Google Scholar 

  15. Csutora P, Strassz A, Boldizsar F, et al: Inhibition of phosphoglucomutase activity by lithium alters cellular calcium homeostasis and signaling in Saccharomyces cerevisiae. Am J Physiol Cell Physiol 289: C58-C67, 2005

    Article  PubMed  CAS  Google Scholar 

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Correspondence to Richard Kellermayer MD, PhD.

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Süle, N., Tészás, A., Kálmán, E. et al. Lithium suppresses epidermal SERCA2 and PMR1 levels in the rat. Pathol. Oncol. Res. 12, 234–236 (2006). https://doi.org/10.1007/BF02893419

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  • DOI: https://doi.org/10.1007/BF02893419

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