Junkai Xie
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Junkai Xie has a total of 17 co-authors. Here are the top co-authors by number of shared publications:
- Alexander A. Chubykin
Department of Biological Sciences, Purdue Institute for Integrative Neuroscience, Purdue Autism Research Center, Purdue University, West Lafayette, IN 47907, USA; Department of Biomedical Engineering, Purdue University, West Lafayette, IN 47907, USA
1 shared publication - Chang Ding
Department of Biological Sciences, Purdue University 4 , West Lafayette, Indiana 47907
1 shared publication - Chongli Yuan
Davidson School of Chemical Engineering, Purdue University, West Lafayette, USA
1 shared publication - Christopher J. Staiger
Department of Botany and Plant Pathology, Purdue University, West Lafayette, IN, USA
1 shared publication - Conwy Zheng
Purdue University, West Lafayette 1 Department of Biological Sciences West Lafayette, IN
1 shared publication - Daniel H. Kim
Purdue University, West Lafayette 1 Department of Biological Sciences West Lafayette, IN
1 shared publication
Latest Publications
- Open Access
- 19 November 2025
- Published by Rockefeller University Press in Journal of Cell Biology
- Vol. 225 (1)
Inwardly rectifying potassium channels promote directional sensing during neutrophil chemotaxis
Potassium channels control membrane potential and various physiological processes, including cell migration. However, the specific role of inwardly rectifying potassium channels in immune cell chemotaxis remains unknown. Here, we demonstrate that inwardly rectifying potassium channels, particularly Kir7.1 (Kcnj13), maintain the resting membrane potential and are crucial for directional sensing during neutrophil chemotaxis. Blocking or knocking out Kir in neutrophils disrupted their ability to sense direction toward different chemoattractants in multiple models. Using genetically encoded voltage indicators, we observed oscillating hyperpolarization during tail retraction in zebrafish neutrophils, with Kir7.1 required for depolarization toward the chemokine source. Focal depolarization via optogenetics biased pseudopod selection and triggered new protrusions, which depended on Gα signaling. Global hyperpolarization caused neutrophils to stall migration. Additionally, Kir influences GPCR signaling activation in dHL-60 cells. This research introduces membrane potential as a key component of the complex feedforward mechanism that links the adaptive and excitable networks necessary to guide immune cells in challenging tissue environments.
- 19 November 2025
- Published by Rockefeller University Press in Journal of Cell Biology
- Vol. 225 (1)
Open AccessInwardly rectifying potassium channels promote directional sensing during neutrophil chemotaxis
Potassium channels control membrane potential and various physiological processes, including cell migration. However, the specific role of inwardly rectifying potassium channels in immune cell chemotaxis remains unknown. Here, we demonstrate that inwardly rectifying potassium channels, particularly Kir7.1 (Kcnj13), maintain the resting membrane potential and are crucial for directional sensing during neutrophil chemotaxis. Blocking or knocking out Kir in neutrophils disrupted their ability to sense direction toward different chemoattractants in multiple models. Using genetically encoded voltage indicators, we observed oscillating hyperpolarization during tail retraction in zebrafish neutrophils, with Kir7.1 required for depolarization toward the chemokine source. Focal depolarization via optogenetics biased pseudopod selection and triggered new protrusions, which depended on Gα signaling. Global hyperpolarization caused neutrophils to stall migration. Additionally, Kir influences GPCR signaling activation in dHL-60 cells. This research introduces membrane potential as a key component of the complex feedforward mechanism that links the adaptive and excitable networks necessary to guide immune cells in challenging tissue environments.