Intravital imaging of neutrophil recruitment in intestinal ischemia-reperfusion injury

S Hashimoto, M Honda, T Takeichi, M Sakisaka… - Biochemical and …, 2018 - Elsevier
S Hashimoto, M Honda, T Takeichi, M Sakisaka, Y Narita, D Yoshii, K Uto, S Sakamoto…
Biochemical and biophysical research communications, 2018Elsevier
Background Neutrophils are known to be key players in innate immunity. Activated
neutrophils induce local inflammation, which results in pathophysiologic changes during
intestinal ischemia-reperfusion injury (IRI). However, most studies have been based on
static assessments, and few have examined real-time intravital neutrophil recruitment. We
herein report a method for imaging and evaluating dynamic changes in the neutrophil
recruitment in intestinal IRI using two-photon laser scanning microscopy (TPLSM). Methods …
Background
Neutrophils are known to be key players in innate immunity. Activated neutrophils induce local inflammation, which results in pathophysiologic changes during intestinal ischemia-reperfusion injury (IRI). However, most studies have been based on static assessments, and few have examined real-time intravital neutrophil recruitment. We herein report a method for imaging and evaluating dynamic changes in the neutrophil recruitment in intestinal IRI using two-photon laser scanning microscopy (TPLSM).
Methods
LysM-eGFP mice were subjected to 45 min of warm intestinal ischemia followed by reperfusion. Mice received an intravenous injection of tetramethylrhodamine isothiocyanate-labeled albumin to visualize the microvasculature. Using a time-lapse TPLSM technique, we directly observed the behavior of neutrophils in intestinal IRI.
Results
We were able to image all layers of the intestine without invasive surgical stress. At low-magnification, the number of neutrophils per field of view continued to increase for 4 h after reperfusion. High-magnification images revealed the presence or absence of blood circulation. At 0–2 h after reperfusion, rolling and adhesive neutrophils increased along the vasculature. At 2–4 h after reperfusion, the irregularity of crypt architecture and transmigration of neutrophils were observed in the lamina propria. Furthermore, TPLSM imaging revealed the villus height, the diameters of the crypt, and the number of infiltrating neutrophils in the crypt. In the IRI group, the villus height 4 h after reperfusion was significantly shorter than in the control group.
Conclusions
TPLSM imaging revealed the real-time neutrophil recruitment in intestinal IRI. Z-stack imaging was useful for evaluating pathophysiological changes in the intestinal wall.
Elsevier