Directional cell motility is required for the development of an organism with proper polarity such as dorso- ventral, anterior-posterior, and left-right symmetry. We have found in Xenopus Laevis that depletion of TRPM7, the first ion channel discovered to have its own kinase domain, results in embryos with severe gastrulation and neural fold closure defects, making TRPM7 the first ion channel shown to have a dramatic effect on this pivotal process during vertebrate development. Surprisingly, our research revealed that incubation of the embryos with excess magnesium or expression of a magnesium transporter reverses this phenotype, giving the first evidence that magnesium plays a critical role in this essential developmental process. Loss of TRPM7's closest homologue TRPM6 in mice has recently been reported to also cause neural tube closure defects. TRPM7 and TRPM6 are known to heterooligomerize when heterologously expressed in tissue culture cells, but reports vary as to whether TRPM6 functions independently as a channel in vivo. Preliminary studies indicate that TRPM7 functions within the non-canonical Wnt pathway to regulate gastrulation and neural fold closure. While TRPM7's mRNA expression remains constant during early development from the zygote to tadpole stage, TRPM6's mRNA expression is upregulated during gastrulation and peaks during neurulation. We propose two specific aims to clarify the functions and regulations of these two channels during early development. The early embryonic lethality caused by deletion of either channel in mice represents a substantial barrier to understanding these channels'functions in vivo. In the first specific aim, we will employ the Xenopus system, in which loss-of-function and gain-of-function experiments are permitted by titrating levels of the protein using antisense morpholino technology, to define the role of TRPM6 and its channel and kinase domains during early development, to determine whether the two channels are functioning in concert, and to determine the impact of these two channels on magnesium homeostasis in the developing embryo. In the second specific aim, we will investigate how the Wnt pathway is regulating TRPM7 and will examine the potential role that 80K-H, a TRPM7- and TRPM6-interacting protein we identified, may have in this process. With their incidence varying among different populations, neural tube closure defects occur at an average rate of 1 per 1000 births and are the second most prevalent malformation, after congenital heart defects, among human pregnancies. Collectively, the proposed experiments should greatly advance our understanding of how these unique bifunctional channels are functioning in vivo, which could lead to new strategies for preventing neural tube closure defects as well as provide new insight into other pathological conditions with which these channels have been associated, including stroke and cancer.

Public Health Relevance

Neural tube defects, such as spina bifida, occur when the neural tube fails to close during embryogenesis and are the second most common birth defect;spina bifida alone affects 166,000 people in the United States with medical costs estimated to be over $70,000 annually for the first 20 years of life. Our research has shown that incubating developing embryos with excess magnesium prevents neural tube defects caused by loss of the TRPM7 ion channel, pointing to critical roles for magnesium and TRPM7 during early development. The proposed research will investigate the functions and regulations of the ion channels TRPM7 and TRPM6 as well as the role of magnesium during embryogenesis, which could help in the development of novel preventive strategies for these devastating birth defects.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
7R01GM080753-07
Application #
8713072
Study Section
Neurotransporters, Receptors, and Calcium Signaling Study Section (NTRC)
Program Officer
Nie, Zhongzhen
Project Start
2007-05-01
Project End
2016-11-30
Budget Start
2013-07-01
Budget End
2013-11-30
Support Year
7
Fiscal Year
2013
Total Cost
$189,383
Indirect Cost
$69,520
Name
Rbhs-Robert Wood Johnson Medical School
Department
Pharmacology
Type
Schools of Medicine
DUNS #
078795875
City
Piscataway
State
NJ
Country
United States
Zip Code
08854
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Liu, Wei; Su, Li-Ting; Khadka, Deepak K et al. (2011) TRPM7 regulates gastrulation during vertebrate embryogenesis. Dev Biol 350:348-57
Su, Li-Ting; Liu, Wei; Chen, Hsiang-Chin et al. (2011) TRPM7 regulates polarized cell movements. Biochem J 434:513-21
Tsai, Yu-Chen; Pestka, Sidney; Wang, Lu-Hai et al. (2011) Interferon-* signaling contributes to Ras transformation. PLoS One 6:e24291
Chen, Hsiang-Chin; Xie, Jia; Zhang, Zheng et al. (2010) Blockade of TRPM7 channel activity and cell death by inhibitors of 5-lipoxygenase. PLoS One 5:e11161
Su, Li-Ting; Chen, Hsiang-Chin; Gonzalez-Pagan, Omayra et al. (2010) TRPM7 activates m-calpain by stress-dependent stimulation of p38 MAPK and c-Jun N-terminal kinase. J Mol Biol 396:858-69