Up-regulation of transient receptor potential canonical 1 (TRPC1) following Sarco(endo)plasmic Reticulum Ca2+ ATPase 2 gene silencing promotes cell survival: A potential role for TRPC1 in Darier's disease

Biswaranjan Pani, Eric Cornatzer, William Cornatzer, Dong Min Shin, Mark R. Pittelkow, Alain Hovnanian, Indu S. Ambudkar, Brij B Singh

Research output: Contribution to journalArticle

63 Citations (Scopus)

Abstract

The mechanism(s) involved in regulation of store operated calcium entry in Darier's disease (DD) is not known. We investigated the distribution and function of transient receptor potential canonical (TRPC) in epidermal skin cells. DD patients demonstrated up-regulation of TRPC1, but not TRPC3, in the squamous layers. Ca2+ influx was significantly higher in keratinocytes obtained from DD patients and showed enhanced proliferation compared with normal keratinocytes. Similar up-regulation of TRPC1 was also detected in epidermal layers of SERCA2+/- mice. HaCaT cells expressed TRPC1 in the plasma membrane. Expression of sarco(endo)plasmic reticulum Ca2+ ATPase (SERCA)2 small interfering RNA (siRNA) in HaCaT cells increased TRPC1 levels and thapsigargin-stimulated Ca2+ influx, which was blocked by store-operated calcium entry inhibitors. Thapsigargin-stimulated intracellular Ca2+ release was decreased in DD cells. DD keratinocytes exhibited increased cell survival upon thapsigargin treatment. Alternatively, overexpression of TRPC1 or SERCA2-SiRNA in HaCaT cells demonstrated resistance to thapsigargin-induced apoptosis. These effects were dependent on external Ca2+ and activation of nuclear factor-κB. Isotretinoin reduced Ca2+ entry in HaCaT cells and decreased survival of HaCaT and DD keratinocytes. These findings put forward a novel consequence of compromised SERCA2 function in DD wherein up-regulation of TRPC1 augments cell proliferation and restrict apoptosis. We suggest that the anti-apoptotic effect of TRPC1 could potentially contribute to abnormal keratosis in DD.

Original languageEnglish (US)
Pages (from-to)4446-4458
Number of pages13
JournalMolecular Biology of the Cell
Volume17
Issue number10
DOIs
StatePublished - Oct 1 2006
Externally publishedYes

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Darier Disease
Reticulum
Calcium-Transporting ATPases
Gene Silencing
Cell Survival
Up-Regulation
Thapsigargin
Keratinocytes
Apoptosis
Calcium
Keratosis
Isotretinoin
Small Interfering RNA
Cell Proliferation
Cell Membrane
Skin

ASJC Scopus subject areas

  • Molecular Biology
  • Cell Biology

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Up-regulation of transient receptor potential canonical 1 (TRPC1) following Sarco(endo)plasmic Reticulum Ca2+ ATPase 2 gene silencing promotes cell survival : A potential role for TRPC1 in Darier's disease. / Pani, Biswaranjan; Cornatzer, Eric; Cornatzer, William; Shin, Dong Min; Pittelkow, Mark R.; Hovnanian, Alain; Ambudkar, Indu S.; Singh, Brij B.

In: Molecular Biology of the Cell, Vol. 17, No. 10, 01.10.2006, p. 4446-4458.

Research output: Contribution to journalArticle

Pani, Biswaranjan ; Cornatzer, Eric ; Cornatzer, William ; Shin, Dong Min ; Pittelkow, Mark R. ; Hovnanian, Alain ; Ambudkar, Indu S. ; Singh, Brij B. / Up-regulation of transient receptor potential canonical 1 (TRPC1) following Sarco(endo)plasmic Reticulum Ca2+ ATPase 2 gene silencing promotes cell survival : A potential role for TRPC1 in Darier's disease. In: Molecular Biology of the Cell. 2006 ; Vol. 17, No. 10. pp. 4446-4458.
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abstract = "The mechanism(s) involved in regulation of store operated calcium entry in Darier's disease (DD) is not known. We investigated the distribution and function of transient receptor potential canonical (TRPC) in epidermal skin cells. DD patients demonstrated up-regulation of TRPC1, but not TRPC3, in the squamous layers. Ca2+ influx was significantly higher in keratinocytes obtained from DD patients and showed enhanced proliferation compared with normal keratinocytes. Similar up-regulation of TRPC1 was also detected in epidermal layers of SERCA2+/- mice. HaCaT cells expressed TRPC1 in the plasma membrane. Expression of sarco(endo)plasmic reticulum Ca2+ ATPase (SERCA)2 small interfering RNA (siRNA) in HaCaT cells increased TRPC1 levels and thapsigargin-stimulated Ca2+ influx, which was blocked by store-operated calcium entry inhibitors. Thapsigargin-stimulated intracellular Ca2+ release was decreased in DD cells. DD keratinocytes exhibited increased cell survival upon thapsigargin treatment. Alternatively, overexpression of TRPC1 or SERCA2-SiRNA in HaCaT cells demonstrated resistance to thapsigargin-induced apoptosis. These effects were dependent on external Ca2+ and activation of nuclear factor-κB. Isotretinoin reduced Ca2+ entry in HaCaT cells and decreased survival of HaCaT and DD keratinocytes. These findings put forward a novel consequence of compromised SERCA2 function in DD wherein up-regulation of TRPC1 augments cell proliferation and restrict apoptosis. We suggest that the anti-apoptotic effect of TRPC1 could potentially contribute to abnormal keratosis in DD.",
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