Zinc is an essential trace element that serves as a cofactor for enzymes in critical biochemical processes and also plays a structural role in numerous proteins. Zinc transporter ZIP4 (ZIP4) is a zinc importer required for dietary zinc uptake in the intestine and other cell types. Studies in cultured cells have reported that zinc stimulates the endocytosis of plasma membrane-localized ZIP4 protein， resulting in reduced cellular zinc uptake. Thus， zinc-regulated trafficking of ZIP4 is a key means for regulating cellular zinc homeostasis， but the underlying mechanisms are not well understood. In this study， we used mutational analysis， immunoblotting， HEK293 cells， and immunofluorescence microscopy to identify a histidine-containing motif (HTH) in the first extracellular loop that is required for high sensitivity to low zinc concentrations in a zinc-induced endocytic response of mouse ZIP4 (mZIP4). Moreover， using synthetic peptides with selective substitutions and truncated mZIP4 variants， we provide evidence that histidine residues in this motif coordinate a zinc ion in mZIP4 homodimers at the plasma membrane. These findings suggest that HTH is an important zinc-sensing motif for eliciting high-affinity zinc-stimulated endocytosis of mZIP4 and provide insight into cellular mechanisms for regulating cellular zinc homeostasis in mammalian cells.