Nitrate (NO 3 −) is a source of plant nutrients and osmolytes, but its delivery machineries under osmotic and low-nutrient stress remain largely unknown. Here, we report that AtICln, an Arabidopsis homolog of the nucleotide-sensitive chloride-conductance regulatory protein family (ICln), is involved in response to osmotic and low-NO 3 − stress. The gene AtICln, encoding plasma membrane-anchored proteins, was upregulated by various osmotic stresses, and its disruption impaired plant tolerance to osmotic stress. Compared with the wild type, the aticln mutant retained lower anions, particularly NO 3 − , and its growth retardation was not rescued by NO 3 − supply under osmotic stress. Interestingly, this mutant also displayed growth defects under low-NO 3 stress, which were accompanied by decreases in NO 3 − accumulation, suggesting that AtICln may facilitate the NO 3 − accumulation under NO 3 − deficiency. Moreover, the low-NO 3 − hypersensitive phenotype of aticln mutant was overridden by the overexpression of NRT1.1, an important NO 3 − transporter in Arabidopsis low-NO 3 − responses. Further genetic analysis in the plants with altered activity of AtICln and NRT1.1 indicated that AtICln and NRT1.1 play a compensatory role in maintaining NO 3 − homeostasis under low-NO 3 − environments.These results suggest that AtICln is involved in cellular NO 3 − accumulation and thus determines osmotic adjustment and low-NO 3 − tolerance in plants.