Uncovering differences in cadmium accumulation capacity of different Ipomoea aquatica cultivars at the level of root cell types

Chuang Shen , Bai-Fei Huang , Qiong Liao , Kai-Feng Chen , Jun-Liang Xin , Ying-Ying Huang

Horticulture Research ›› 2025, Vol. 12 ›› Issue (6) : 77

PDF (2465KB)
Horticulture Research ›› 2025, Vol. 12 ›› Issue (6) :77 DOI: 10.1093/hr/uhaf077
Articles
research-article

Uncovering differences in cadmium accumulation capacity of different Ipomoea aquatica cultivars at the level of root cell types

Author information +
History +
PDF (2465KB)

Abstract

Water spinach (Ipomoea aquatica) can accumulate cadmium (Cd) even in mildly contaminated soils, but the roles of its root tip cell types in Cd fixation and transport remain unclear. Single-cell RNA sequencing revealed nine cell types in root tips in both the QLQ cultivar (low Cd accumulation) and the T308 cultivar (high Cd accumulation). High expression of LAC2 and PER72 in the QLQ epidermis was associated with enhanced lignin deposition, which may facilitate fixation of Cd and reduce its translocation to the shoot. In T308, PER72 and hormone-related genes (PIN1, ARF8, IAA17, and EIN3) were upregulated, which was hypothesized to promote xylem and trichoblast development, potentially facilitating Cd uptake and transport. Fluorescence assays suggested that the higher pectin demethylation and lignin content in QLQ may limit Cd movement, whereas the more developed tissues in T308 may contribute to increased Cd accumulation in the shoots. These findings clarify the mechanisms by which Cd accumulates in water spinach and offer insights into mitigating Cd uptake in crops.

Cite this article

Download citation ▾
Chuang Shen, Bai-Fei Huang, Qiong Liao, Kai-Feng Chen, Jun-Liang Xin, Ying-Ying Huang. Uncovering differences in cadmium accumulation capacity of different Ipomoea aquatica cultivars at the level of root cell types. Horticulture Research, 2025, 12(6): 77 DOI:10.1093/hr/uhaf077

登录浏览全文

4963

注册一个新账户 忘记密码

Acknowledgments

This study was supported by the National Natural Science Foundation of China (Grant No. 42107039 and 42007144), Natural Science Foundation of Hunan Province, China (Grant No. 2022JJ40139), Scientific Research Foundation of Hunan Provincial Education Department (Grant No. 24B0838) and College Students Research Learning and Innovative Experiment Project of Hunan Province (Grant No. S202311528145). In addition, I would like to express my deepest gratitude to Mr. Chen (B) and Mr. Zhang (Pao) for their consistent provision of nutritional support and wellness resources throughout this research. Their contributions significantly alleviated physical challenges during intensive study periods, enabling sustained focus on this work. May this collaborative spirit inspire continued growth within our scholarly community.

Author Contributions

A total of six authors participated in this work, including Chuang Shen, Bai-Fei Huang, Qiong Liao, Kai-Feng Chen, Jun-Liang Xin, and Ying-Ying Huang. Conception and design of study: Chuang Shen and Ying-Ying Huang. Acquisition of data: Chuang Shen, Bai-Fei Huang, Qiong Liao, Kai-Feng Chen, Jun-Liang Xin. Analysis and/or interpretation of data: Chuang Shen, Bai-Fei Huang, Ying-Ying Huang. Drafting the manuscript: Chuang Shen and Bai-Fei Huang. Revising the manuscript critically for important intellectual content: Chuang Shen and Ying-Ying Huang.

Data availability

The raw scRNA-seq data from this study have been deposited in the China National Center for Bioinformation under BioProject ID: PRJCA029540. Similarly, the raw bulk RNA-seq data are available in the same repository under BioProject ID: PRJCA029575.

Conflict of interest statement:

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Supplementary data

Supplementary data is available at Horticulture Research online.

References

[1]

Zhong S, Li X, Fang L. et al. Multifunctional roles of zinc in cadmium transport in soil-Rice systems: novel insights from stable isotope fractionation and gene expression. Environ Sci Technol. 2024; 58:12467-76

[2]

Honma T, Ohba H, Kaneko-Kadokura A. et al. Optimal soil eh, pH, and water Management for Simultaneously Minimizing Arsenic and Cadmium Concentrations in Rice grains. Environ Sci Technol. 2016; 50:4178-85

[3]

Podar D, Maathuis FJM. The role of roots and rhizosphere in providing tolerance to toxic metals and metalloids. Plant Cell Environ. 2022; 45:719-36

[4]

Yang H, Yu H, Wu Y. et al. Nitric oxide amplifies cadmium binding in root cell wall of a high cadmium-accumulating rice (Oryza sativa L.) line by promoting hemicellulose synthesis and pectin demethylesterification. Ecotoxicol Environ Saf. 2022; 234: 113404

[5]

Noor I, Sohail H, Akhtar MT. et al. From stress to resilience: unraveling the molecular mechanisms of cadmium toxicity, detoxification and tolerance in plants. Sci Total Environ. 2024; 954:176462

[6]

Mi B, Xiao W, Tu N. et al. Selection of pollution-safe head cab-bage: interaction of multiple heavy metals in soil on bioaccu-mulation and transfer. Food Chem. 2024; 452:139615

[7]

Shen C, Fu H-L, Liao Q. et al. Transcriptome analysis and phys-iological indicators reveal the role of sulfur in cadmium accu-mulation and transportation in water spinach (Ipomoea aquatica Forsk.). Ecotoxicol Environ Saf. 2021; 225:112787

[8]

Xiong J, Yang Y, Fu G. et al. Novel roles of hydrogen peroxide (H2O2) in regulating pectin synthesis and demethylesterifica-tion in the cell wall of rice (Oryza sativa) root tips. New Phytol. 2015; 206:118-26

[9]

Shen C, Fu H, Huang B. et al. Physiological and molecular mech-anisms of boron in alleviating cadmium toxicity in Capsicum annuum. Sci Total Environ. 2023; 903:166264

[10]

Wang P, Yang B, Wan H. et al. The differences of cell wall in roots between two contrasting soybean cultivars exposed to cadmium at young seedlings. Environ Sci Pollut Res Int. 2018; 25:29705-14

[11]

Di X, Jing R, Qin X. et al. The role and transcriptomic mecha-nism of cell wall in the mutual antagonized effects between selenium nanoparticles and cadmium in wheat. J Hazard Mater. 2024; 472:134549

[12]

Peng C, Song H, Zhao Z. et al. Foliar spraying with a mixture of transpiration inhibitor-rhamnolipid reduces the Cd content in rice grains. Sci Total Environ. 2023; 885:163844

[13]

Zhang T-Q, Xu Z-G, Shang G-D. et al. A single-cell RNA sequenc-ing profiles the developmental landscape of Arabidopsis root. Mol Plant. 2019; 12:648-60

[14]

Drapek C, Sparks EE, Benfey PN. Uncovering gene regulatory networks controlling plant cell differentiation. Trends Genet TIG. 2017; 33:529-39

[15]

Kuang L, Yan T, Gao F. et al. Multi-omics analysis reveals differ-ential molecular responses to cadmium toxicity in rice root tip and mature zone. J Hazard Mater. 2024; 462:132758

[16]

Chen X, Ru Y, Takahashi H. et al. Single-cell transcriptomic anal-ysis of pea shoot development and cell-type-specific responses to boron deficiency. Plant J Cell Mol Biol. 2024; 117:302-22

[17]

Piacentini D, Della Rovere F, Bertoldi I. et al. Peroxisomal PEX7 receptor affects cadmium-induced ROS and Auxin homeostasis in Arabidopsis root system. Antioxid Basel Switz. 2021; 10:1494

[18]

Lux A, Martinka M, Vaculík M. et al. Root responses to cadmium in the rhizosphere: a review. JExp Bot. 2011; 62:21-37

[19]

Kolodziejczyk AA, Kim JK, Svensson V. et al. The technology and biology of single-cell RNA sequencing. Mol Cell. 2015; 58:610-20

[20]

Bai Y, Liu H, Lyu H. et al. Development of a single-cell atlas for woodland strawberry (Fragaria vesca) leaves during early Botrytis cinerea infection using single cell RNA-seq. Hortic Res. 2022;9:uhab055

[21]

Zong J, Wang L, Zhu L. et al. A rice single cell transcriptomic atlas defines the developmental trajectories of rice floret and inflorescence meristems. New Phytol. 2022; 234:494-512

[22]

Wang Y, Huan Q, Li K. et al. Single-cell transcriptome atlas of the leaf and root of rice seedlings. J Genet Genomics Yi Chuan Xue Bao. 2021; 48:881-98

[23]

Wendrich JR, BaoJun Y, Niels V. et al. Vascular transcription factors guide plant epidermal responses to limiting phosphate conditions. Science. 2020;370:eaay4970

[24]

Xin J, Huang B, Yang Z. et al. Comparison of cadmium subcellular distribution in different organs of two water spinach (Ipomoea aquatica Forsk.) cultivars. Plant Soil. 2013; 372:431-44

[25]

Balcerowicz D, Schoenaers S, Vissenberg K. Cell fate determi-nation and the switch from diffuse growth to planar polarity in Arabidopsis root epidermal cells. Front Plant Sci. 2015; 6: 1163

[26]

Huang Y-Y, Shen C, Fu H-L. et al. Proteomic and biochemical evidence involving root Cell Wall biosynthesis and modification, tricarboxylic acid cycle, and glutathione metabolism in cultivar-dependent Cd accumulation of water spinach (Ipomoea aquatica). J Agric Food Chem. 2023; 71:2784-94

[27]

An Y, Jiao X, Yang S. et al. Evaluation of novel promoters for vascular tissue-specific gene expression in Populus. Plant Sci. 2024; 344:112083

[28]

Liang X, Ma Z, Ke Y. et al. Single-cell transcriptomic analyses reveal cellular and molecular patterns of rubber tree response to early powdery mildew infection. Plant Cell Environ. 2023; 46: 2222-37

[29]

Liu J, Lv Y, Li M. et al. Peroxidase in plant defense: novel insights for cadmium accumulation in rice (Oryza sativa L.). J Hazard Mater. 2024; 474:134826

[30]

Rahoui S, Martinez Y, Sakouhi L. et al. Cadmium-induced changes in antioxidative systems and differentiation in roots of contrasted Medicago truncatula lines. Protoplasma. 2017; 254: 473-89

[31]

Wang X-S, Fu H-L, Gong F-Y. et al. Lignin side chain region participates in Cd detoxification related to the cultivar-dependent Cd accumulation in Brassica chinensis L. J Hazard Mater. 2020; 392:122264

[32]

Dong Q, Wu Y, Li B. et al. Multiple insights into lignin-mediated cadmium detoxification in rice (Oryza sativa). J Hazard Mater. 2023; 458:131931

[33]

Ramachandran P, Wang G, Augstein F. et al. Continuous root xylem formation and vascular acclimation to water deficit involves endodermal ABA signalling via miR165. Dev Camb Engl. 2018;145:dev159202

[34]

von der Mark C, Cruz TMD, Blanco-Touriñan N. et al. Bipartite phosphoinositide-dependent modulation of auxin signaling dur-ing xylem differentiation in Arabidopsis thaliana roots. New Phytol. 2022; 236:1734-47

[35]

Ben-Targem M, Ripper D, Bayer M. et al. Auxin and gibberellin signaling cross-talk promotes hypocotyl xylem expansion and cambium homeostasis. JExp Bot. 2021; 72:3647-60

[36]

Agustí J, Blázquez MA. Plant vascular development: mecha-nisms and environmental regulation. Cell Mol Life Sci. 2020; 77: 3711-28

[37]

de Silva NDG, Cholewa E, Ryser P. Effects of combined drought and heavy metal stresses on xylem structure and hydraulic conductivity in red maple (Acer rubrum L.). JExp Bot. 2012; 63: 5957-66

[38]

TaoQ, JupaR, DongQ. et al. Abscisic acid-mediated modi-fications in water transport continuum are involved in cad-mium hyperaccumulation in sedum alfredii. Chemosphere. 2021; 268:129339

[39]

Tao J, Lu L. Advances in genes-encoding transporters for cad-mium uptake, translocation, and accumulation in plants. Toxics. 2022; 10:411

[40]

Hendriks P-W, Ryan PR, Hands P. et al. Selection for early shoot vigour in wheat increases root hair length but reduces epidermal cell size of roots and leaves. JExp Bot. 2022; 73:2499-510

[41]

Zhou M, Zhang LL, Ye JY. et al. Knockout of FER decreases cadmium concentration in roots of Arabidopsis thaliana by inhibiting the pathway related to iron uptake. Sci Total Environ. 2021; 798:149285

[42]

Cui X, Wang S, Huang Y. et al. Arabidopsis SYP121 acts as an ROP2 effector in the regulation of root hair tip growth. Mol Plant. 2022; 15:1008-23

[43]

Feng Y, Xu P, Li B. et al. Ethylene promotes root hair growth through coordinated EIN3/EIL1 and RHD6/RSL1 activity in Ara-bidopsis. Proc Natl Acad Sci USA. 2017; 114:13834-9

[44]

Mangano S, Denita-Juarez SP, Choi H-S. et al. Molecular link between auxin and ROS-mediated polar growth. Proc Natl Acad Sci USA. 2017; 114:5289-94

[45]

Loix C, Huybrechts M, Vangronsveld J. et al. Reciprocal interac-tions between cadmium-induced cell wall responses and oxida-tive stress in plants. Front Plant Sci. 2017; 8:1867

[46]

Lao R, Guo Y, Hao W. et al. The role of lignin in the com-partmentalization of cadmium in maize roots is enhanced by mycorrhiza. J Fungi. 2023; 9:852

[47]

Yang F, Chang YZ, Zheng YT. et al. Physiological and transcrip-tomic characterization of cadmium toxicity in Moso bamboo (Phyllostachys edulis), a non-timber forest species. Tree Physiol. 2023; 43:1250-64

[48]

Trapnell C, Cacchiarelli D, Grimsby J. et al. The dynamics and regulators of cell fate decisions are revealed by pseudotemporal ordering of single cells. Nat Biotechnol. 2014; 32:381-6

[49]

Yang JL, Li YY, Zhang YJ. et al. Cell wall polysaccharides are specifically involved in the exclusion of aluminum from the rice root apex. Plant Physiol. 2008; 146:602-11

[50]

Gao MY, Chen XW, Huang WX. et al. Cell wall modification induced by an arbuscular mycorrhizal fungus enhanced cad-mium fixation in rice root. J Hazard Mater. 2021; 416:125894

[51]

Baldacci-Cresp F, Spriet C, Twyffels L. et al. A rapid and quantita-tive safranin-based fluorescent microscopy method to evaluate cell wall lignification. Plant J. 2020; 102:1074-89

AI Summary AI Mindmap
PDF (2465KB)

19

Accesses

0

Citation

Detail

Sections
Recommended

AI思维导图

/