Curcumin derivatives promote Schwann cell differentiation and improve neuropathy in R98C CMT1B mice

Ágnes Patzkó, Yunhong Bai, Mario da Cunha Saporta, István Katona, Xingyao Wu, Domenica Vizzuso, M. Laura Feltri, Suola Wang, Lisa M. Dillon, John Kamholz, Daniel Kirschner, Fazlul H. Sarkar, Lawrence Wrabetz, Michael E. Shy

Research output: Contribution to journalArticle

58 Citations (Scopus)

Abstract

Charcot-Marie-Tooth disease type 1B is caused by mutations in myelin protein zero. R98C mice, an authentic model of early onset Charcot-Marie-Tooth disease type 1B, develop neuropathy in part because the misfolded mutant myelin protein zero is retained in the endoplasmic reticulum where it activates the unfolded protein response. Because oral curcumin, a component of the spice turmeric, has been shown to relieve endoplasmic reticulum stress and decrease the activation of the unfolded protein response, we treated R98C mutant mice with daily gastric lavage of curcumin or curcumin derivatives starting at 4 days of age and analysed them for clinical disability, electrophysiological parameters and peripheral nerve morphology. Heterozygous R98C mice treated with curcumin dissolved in sesame oil or phosphatidylcholine curcumin performed as well as wild-type littermates on a rotarod test and had increased numbers of large-diameter axons in their sciatic nerves. Treatment with the latter two compounds also increased compound muscle action potential amplitudes and the innervation of neuromuscular junctions in both heterozygous and homozygous R98C animals, but it did not improve nerve conduction velocity, myelin thickness, G-ratios or myelin period. The expression of c-Jun and suppressed cAMP-inducible POU (SCIP)-transcription factors that inhibit myelination when overexpressed-was also decreased by treatment. Consistent with its role in reducing endoplasmic reticulum stress, treatment with curcumin dissolved in sesame oil or phosphatidylcholine curcumin was associated with decreased X-box binding protein (XBP1) splicing. Taken together, these data demonstrate that treatment with curcumin dissolved in sesame oil or phosphatidylcholine curcumin improves the peripheral neuropathy of R98C mice by alleviating endoplasmic reticulum stress, by reducing the activation of unfolded protein response and by promoting Schwann cell differentiation.

Original languageEnglish (US)
Pages (from-to)3551-3566
Number of pages16
JournalBrain
Volume135
Issue number12
DOIs
StatePublished - Jan 1 2012
Externally publishedYes

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Curcumin
Schwann Cells
Cell Differentiation
Sesame Oil
Unfolded Protein Response
Endoplasmic Reticulum Stress
Myelin P0 Protein
Phosphatidylcholines
Charcot-Marie-Tooth Disease
Myelin Sheath
POU Domain Factors
Rotarod Performance Test
Gastric Lavage
Protein Splicing
Curcuma
Spices
Neuromuscular Junction
Neural Conduction
Peripheral Nervous System Diseases
Sciatic Nerve

Keywords

  • Charcot-Marie-Tooth disease 1B
  • curcumin
  • myelin protein zero
  • peripheral neuropathy
  • unfolded protein response

ASJC Scopus subject areas

  • Clinical Neurology

Cite this

Curcumin derivatives promote Schwann cell differentiation and improve neuropathy in R98C CMT1B mice. / Patzkó, Ágnes; Bai, Yunhong; da Cunha Saporta, Mario; Katona, István; Wu, Xingyao; Vizzuso, Domenica; Feltri, M. Laura; Wang, Suola; Dillon, Lisa M.; Kamholz, John; Kirschner, Daniel; Sarkar, Fazlul H.; Wrabetz, Lawrence; Shy, Michael E.

In: Brain, Vol. 135, No. 12, 01.01.2012, p. 3551-3566.

Research output: Contribution to journalArticle

Patzkó, Á, Bai, Y, da Cunha Saporta, M, Katona, I, Wu, X, Vizzuso, D, Feltri, ML, Wang, S, Dillon, LM, Kamholz, J, Kirschner, D, Sarkar, FH, Wrabetz, L & Shy, ME 2012, 'Curcumin derivatives promote Schwann cell differentiation and improve neuropathy in R98C CMT1B mice', Brain, vol. 135, no. 12, pp. 3551-3566. https://doi.org/10.1093/brain/aws299
Patzkó, Ágnes ; Bai, Yunhong ; da Cunha Saporta, Mario ; Katona, István ; Wu, Xingyao ; Vizzuso, Domenica ; Feltri, M. Laura ; Wang, Suola ; Dillon, Lisa M. ; Kamholz, John ; Kirschner, Daniel ; Sarkar, Fazlul H. ; Wrabetz, Lawrence ; Shy, Michael E. / Curcumin derivatives promote Schwann cell differentiation and improve neuropathy in R98C CMT1B mice. In: Brain. 2012 ; Vol. 135, No. 12. pp. 3551-3566.
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abstract = "Charcot-Marie-Tooth disease type 1B is caused by mutations in myelin protein zero. R98C mice, an authentic model of early onset Charcot-Marie-Tooth disease type 1B, develop neuropathy in part because the misfolded mutant myelin protein zero is retained in the endoplasmic reticulum where it activates the unfolded protein response. Because oral curcumin, a component of the spice turmeric, has been shown to relieve endoplasmic reticulum stress and decrease the activation of the unfolded protein response, we treated R98C mutant mice with daily gastric lavage of curcumin or curcumin derivatives starting at 4 days of age and analysed them for clinical disability, electrophysiological parameters and peripheral nerve morphology. Heterozygous R98C mice treated with curcumin dissolved in sesame oil or phosphatidylcholine curcumin performed as well as wild-type littermates on a rotarod test and had increased numbers of large-diameter axons in their sciatic nerves. Treatment with the latter two compounds also increased compound muscle action potential amplitudes and the innervation of neuromuscular junctions in both heterozygous and homozygous R98C animals, but it did not improve nerve conduction velocity, myelin thickness, G-ratios or myelin period. The expression of c-Jun and suppressed cAMP-inducible POU (SCIP)-transcription factors that inhibit myelination when overexpressed-was also decreased by treatment. Consistent with its role in reducing endoplasmic reticulum stress, treatment with curcumin dissolved in sesame oil or phosphatidylcholine curcumin was associated with decreased X-box binding protein (XBP1) splicing. Taken together, these data demonstrate that treatment with curcumin dissolved in sesame oil or phosphatidylcholine curcumin improves the peripheral neuropathy of R98C mice by alleviating endoplasmic reticulum stress, by reducing the activation of unfolded protein response and by promoting Schwann cell differentiation.",
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