An optical system for noninvasive microscopy of psoriatic mice in vivo.
Yiting LuYujie ZhuXiaohui ZhaoMeng PanHao HePublished in: Journal of biophotonics (2022)
Psoriasis is a chronic inflammatory skin disease involved with both complex morphological changes of skin and immune processes. The clinical diagnostics and research of psoriasis often require invasive biopsy which lacks their real-time dynamics in vivo. Here we report a noninvasive microscopic system developed by combining in vivo fluorescent microscopy, optical clearing, and immunolabeling to enable real-time imaging of immune cells and cytokines in blood flow in psoriatic animal models. The vascular morphology and time-lapse kinetics of interleukin (IL)-23, IL-17, tumor necrosis factor-α, and CD4+ cells in blood are captured at submicron resolution through the thickening epidermis and opaque scales during the development of psoriasis in vivo. Our data suggest IL-23 recruits CD4+ cells to release IL-17 in blood that further leaks out in the psoriatic skin area. This optical system enables noninvasive and real-time assessment of immune molecules and cells in vivo, providing good potential for medical researches on psoriasis.
Keyphrases
- high resolution
- induced apoptosis
- rheumatoid arthritis
- cell cycle arrest
- blood flow
- high speed
- single molecule
- healthcare
- ankylosing spondylitis
- disease activity
- oxidative stress
- soft tissue
- atopic dermatitis
- endoplasmic reticulum stress
- type diabetes
- systemic lupus erythematosus
- climate change
- quantum dots
- machine learning
- optical coherence tomography
- big data
- cell death
- electronic health record
- adipose tissue
- skeletal muscle
- metabolic syndrome
- drug induced
- risk assessment
- nk cells