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The pathway of transmembrane cadmium influx via calcium-permeable channels and its spatial characteristics along rice root.

ABSTRACT: To develop elite crops with low cadmium (Cd), a fundamental understanding of the mechanism of Cd uptake by crop roots is necessary. Here, a new mechanism for Cd2+ entry into rice root cells was investigated. The results showed that Cd2+ influx in rice roots exhibited spatially and temporally dynamic patterns. There was a clear longitudinal variation in Cd uptake along rice roots, with the root tip showing much higher Cd2+ influx and concentration than the root mature zone, which might be due to the much higher expression of the well-known Cd transporter genes OsIRT1, OsNRAMP1, OsNRAMP5, and OsZIP1 in the root tip. Both the net Cd2+ influx and the uptake of Cd in rice roots were highly inhibited by ion channel blockers Gd3+ and TEA+, supplementation of Ca2+ and K+, and the plasma membrane H+-ATPase inhibitor vanadate, with Gd3+ and Ca2+ showing the most inhibitory effects. Furthermore, Ca2+- or Gd3+-induced reduction in Cd2+ influx and Cd uptake did not coincide with the expression of Cd transporter genes, but with that of two Ca channel genes, OsAAN4 and OsGLR3.4. These results indicate that Cd transporters are in part responsible for Cd2+ entry into rice root, and provide a new perspective that the Ca channels OsAAN4 and OsGLR3.4 might play an important role in rice root Cd uptake.

SUBMITTER: Chen X

PROVIDER: S-EPMC6184580 | biostudies-literature | 2018 Oct

REPOSITORIES: biostudies-literature

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The pathway of transmembrane cadmium influx via calcium-permeable channels and its spatial characteristics along rice root.

Chen Xiaohui X Ouyang Younan Y Fan Yicong Y Qiu Boyin B Zhang Guoping G Zeng Fanrong F

Journal of experimental botany 20181001 21

To develop elite crops with low cadmium (Cd), a fundamental understanding of the mechanism of Cd uptake by crop roots is necessary. Here, a new mechanism for Cd2+ entry into rice root cells was investigated. The results showed that Cd2+ influx in rice roots exhibited spatially and temporally dynamic patterns. There was a clear longitudinal variation in Cd uptake along rice roots, with the root tip showing much higher Cd2+ influx and concentration than the root mature zone, which might be due to ...[more]

PMID: 30099559

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Project description:1. In this study, intracellular Ca(2+) was measured as the Fura-2 ratio (R) of fluorescence excited at 340 and 380 nm (F(340)/F(380)) in nonpressurized rat mesenteric small arterioles ( (lumen diameter) 10-25 microm). 2. The response to depolarization using 75 mm KCl was an increase in R from a baseline of 0.96+/-0.01 ([Ca(2+)](i) approximately 74 nm) to 1.04+/-0.01 ( approximately 128 nm) (n=80). The response to 75 mm K(+) was reversibly abolished in Ca(2+)-free physiological saline solution, whereas phentolamine (10 microm) or tetrodotoxin (1 microm) had no effects. LaCl(3) (200 microm) inhibited 61+/-9% of the response. 3. A [K(+)]-response curve indicated that the Ca(2+) response was activated between 15 and 25 mm K(+). The data suggest that the Ca(2+) response was caused by the activation of voltage-dependent Ca(2+) channels. 4. Mibefradil use dependently inhibited the Ca(2+) response to 75 mm K(+) by 29+/-2% (100 nm), 73+/-7% (1 microm) or 89+/-7% (10 microm). Pimozide (500 nm) use dependently inhibited the Ca(2+) response by 85+/-1%. 5. Nifedipine (1 microm) inhibited the Ca(2+) response to 75 mm K(+) by 41+/-12%. The response was not inhibited by calciseptine (500 nm), omega-agatoxin IVA (100 nm), omega-conotoxin MVIIA (500 nm), or SNX-482 (100 nm). 6. Using reverse transcriptase-polymerase chain reaction, it was shown that neither Ca(V)2.1a (P-type) nor Ca(V)2.1b (Q-type) voltage-dependent Ca(2+) channels were expressed in mesenteric arterioles, whereas the Ca(V)3.1 (T-type) channel was expressed. Furthermore, no amplification products were detected when using specific primers for the beta(1b), beta(2), or beta(3) auxiliary subunits of high-voltage-activated Ca(2+) channels. 7. The results suggest that the voltage-dependent Ca(2+) channel activated by sustained depolarization in mesenteric arterioles does not classify as any of the high-voltage-activated channels (L-, P/Q-, N-, or R-type), but is likely to be a T-type channel. The possibility that the sustained Ca(2+) influx observed was the result of a T-type window current is discussed.

Dataset Information

The pathway of transmembrane cadmium influx via calcium-permeable channels and its spatial characteristics along rice root.

Publications

The pathway of transmembrane cadmium influx via calcium-permeable channels and its spatial characteristics along rice root.

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