Adaptive Optical Two-Photon Fluorescence Microscopy Probes Cellular Organization of Ocular Lenses In Vivo

• Published in: Investigative ophthalmology & visual science Vol. 64; no. 7; p. 20
• Main Authors: Paidi, Santosh Kumar, Zhang, Qinrong, Yang, Yuhan, Xia, Chun-Hong, Ji, Na, Gong, Xiaohua
• Format: Journal Article
• Language: English
• Published: United States Association for Research in Vision and Ophthalmology 12.06.2023; The Association for Research in Vision and Ophthalmology
• Subjects: 60 APPLIED LIFE SCIENCES; Animals; Epithelial Cells; Eye; Lens; Lens, Crystalline; Mammals; Microscopy, Fluorescence; Ophthalmology; Photons
• ISSN: 1552-5783; 0146-0404; 1552-5783
• DOI: 10.1167/iovs.64.7.20

The mammalian ocular lens is an avascular multicellular organ that grows continuously throughout life. Traditionally, its cellular organization is investigated using dissected lenses, which eliminates in vivo environmental and structural support. Therefore, in vivo optical imaging methods for studying lenses in their native context in live animals are urgently needed. Here, we demonstrated that two-photon fluorescence microscopy can visualize lens cells in vivo. To maintain subcellular resolution at depth, we used adaptive optics to correct aberrations owing to ocular and lens tissues, which led to substantial signal and resolution improvements. Imaging lens cells up to 980 µm deep, we observed novel cellular organizations including suture-associated voids, enlarged vacuoles, and large cavities, contrary to the conventional view of a highly ordered organization. We tracked these features longitudinally over weeks and observed the incorporation of new cells during growth. Taken together, noninvasive longitudinal in vivo imaging of lens morphology using adaptive optics two-photon fluorescence microscopy will allow us to observe the development or alterations of lens cellular organization in living animals directly.