Tropomodulin 1 Regulation of Actin Is Required for the Formation of Large Paddle Protrusions Between Mature Lens Fiber Cells

PURPOSE. To elucidate the proteins required for specialized small interlocking protrusions and large paddle domains at lens fiber cell tricellular junctions (vertices), we developed a novel method to immunostain single lens fibers and studied changes in cell morphology due to loss of tropomodulin 1 (Tmod1), an F-actin pointed end-capping protein. METHODS. We investigated F-actin and F-actin-binding protein localization in interdigitations of Tmod1(+/+) and Tmod1(-/-) single mature lens fibers. RESULTS. F-actin-rich small protrusions and large paddles were present along cell vertices of Tmod1(+/+) mature fibers. In contrast, Tmod1(-/-) mature fiber cells lack normal paddle domains, while small protrusions were unaffected. In Tmod1(+/+) mature fibers, Tmod1, beta 2-spectrin, and a-actinin are localized in large puncta in valleys between paddles; but in Tmod1(-/-) mature fibers, b2-spectrin was dispersed while alpha-actinin was redistributed at the base of small protrusions and rudimentary paddles. Fimbrin and Arp3 (actin-related protein 3) were located in puncta at the base of small protrusions, while N-cadherin and ezrin outlined the cell membrane in both Tmod1(+/+) and Tmod1(-/-) mature fibers. CONCLUSIONS. These results suggest that distinct F-actin organizations are present in small protrusions versus large paddles. Formation and/or maintenance of large paddle domains depends on a beta 2-spectrin-actin network stabilized by Tmod1. alpha-Actinin-crosslinked F-actin bundles are enhanced in absence of Tmod1, indicating altered cytoskeleton organization. Formation of small protrusions is likely facilitated by Arp3-branched and fimbrin-bundled Factin networks, which do not depend on Tmod1. This is the first work to reveal the F-actinassociated proteins required for the formation of paddles between lens fibers.