Ischemia and reperfusion injury in superficial inferior epigastric artery-based vascularized lymph node flaps

• Published in: PloS one 2020-01, Vol.15 (1), p.e0227599-e0227599
• Main Authors: Perrault, David P, Lee, Gene K, Bouz, Antoun, Sung, Cynthia, Yu, Roy, Pourmoussa, Austin J, Park, Sun Young, Kim, Gene H, Jiao, Wan, Patel, Ketan M, Hong, Young-Kwon, Wong, Alex K
• Format: Article
• Language: English
• Subjects: Animals; Apoptosis; Biology and Life Sciences; Biomarkers; CD3 antigen; CD31 antigen; CD45 antigen; Cell death; Collagen; Cytokines; Cytology; Dissection; Epigastric Arteries - physiopathology; Epigastric Arteries - surgery; Female; Femoral Artery - physiopathology; Fibrosis; Flaps; Fluorescence; Histology; Inflammation; Injury analysis; Ischemia; Ischemia - physiopathology; Lymph; Lymph nodes; Lymph Nodes - blood supply; Lymph Nodes - physiopathology; Lymphatic system; Lymphedema; Lymphedema - surgery; Male; Medical research; Medicine; Medicine and Health Sciences; Morphology; Nodes; Ostomy; Plastic surgery; Rats; Rats, Sprague-Dawley; Reperfusion; Reperfusion Injury - physiopathology; Surgical Flaps - blood supply; Tissues; Tumor necrosis factor-α; Veins & arteries
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/JOURNAL.PONE.0227599

Vascularized lymph node transfer (VLNT) is a promising treatment modality for lymphedema; however, how lymphatic tissue responds to ischemia has not been well defined. This study investigates the cellular changes that occur in lymph nodes in response to ischemia and reperfusion. Lymph node containing superficial epigastric artery-based groin flaps were isolated in Prox-1 EGFP rats which permits real time identification of lymphatic tissue by green fluorescence during flap dissection. Flaps were subjected to ischemia for either 1, 2, 4, or 8 hours, by temporarily occluding the vascular pedicle. Flaps were harvested after 0 hours, 24 hours, or 5 days of reperfusion. Using EGFP signal guidance, lymph nodes were isolated from the flaps and tissue morphology, cell apoptosis, and inflammatory cytokines were quantified and analyzed via histology, immunostaining, and rtPCR. There was a significant increase in collagen deposition and tissue fibrosis in lymph nodes after 4 and 8 hours of ischemia compared to 1 and 2 hours, as assessed by picrosirius red staining. Cell apoptosis significantly increased after 4 hours of ischemia in all harvest times. In tissue subject to 4 hours of ischemia, longer reperfusion periods were associated with increased rates of CD3+ and CD45+ cell apoptosis. rtPCR analysis demonstrated significantly increased expression of CXCL1/GRO-α with 2 hours of ischemia and increased PECAM-1 and TNF-α expression with 1 hour of ischemia. Significant cell death and changes in tissue morphology do not occur until after 4 hours of ischemia; however, analysis of inflammatory biomarkers suggests that ischemia reperfusion injury can occur with as little as 2 hours of ischemia.