Rationally Designed Two-Photon Ratiometric Elastase Probe for Investigating Inflammatory Bowel Disease

• Published in: Analytical chemistry (Washington) 2022-01, Vol.94 (2), p.1373-1381
• Main Authors: Sarkar, Sourav, Shil, Anushree, Nandy, Madhurima, Singha, Subhankar, Reo, Ye Jin, Yang, Yun Jae, Ahn, Kyo Han
• Format: Article
• Language: English
• Subjects: Animals; Chemistry; Colitis; Colon; Duodenum; Elastase; Fluorescence; Immune response; Immune system; Inflammation; Inflammatory bowel disease; Inflammatory bowel diseases; Inflammatory Bowel Diseases - diagnosis; Inflammatory Bowel Diseases - diagnostic imaging; Intestine; Leukocyte Elastase; Leukocyte migration; Leukocytes (neutrophilic); Liver; Mice; Neutrophils; Organs; Photons; Serine proteinase; Small intestine
• ISSN: 0003-2700; 1520-6882
• DOI: 10.1021/acs.analchem.1c04646

Elastase, a serine protease, plays important roles in our body in food digestion and defence against pathogens. Particularly, the elastase present in neutrophils is directly associated with inflammatory bowel disease (IBD). Through a rational approach, we have developed a fluorescent elastase probe that has multiple advantages for biological applications including two-photon ratiometric imaging capability. Using the probe, which is capable of detecting intracellular elastase activity associated with inflammation, we have investigated elastase level changes in various mouse organs under an IBD condition for the first time. The results reveal notably higher elastase levels in the liver and duodenum of the healthy mice than in the other investigated organs. Under the IBD condition, we observed significant elastase level changes in the liver, duodenum, colon, and lung. The downregulation of elastase in the liver under the IBD condition suggests migration of neutrophils into the upregulated organs. The notable upregulation of elastase in the duodenum is explained by self-production of elastase, in addition to the neutrophil migration from the liver. We have observed little elastase level changes in selected organs of immune-deficient mice raised under the normal and IBD conditions, which supports the neutrophil migration as the reason for perturbed elastase activity in the healthy mice. The results also suggest an important role of the liver in maintaining the immune response associated with the inflammation-induced elastase level changes. The probe offers an ideal tool for mapping neutrophil migration in body. Further understanding of the elastase-associated biology and diagnosis of IBD by monitoring affected organs are anticipated using the probe.