脂筏标记蛋白 flotillin FloA 驱动质膜 H⁺-ATPase PmaA 重定位以应对钙胁迫

by Moemi Kawashima, Thomas Krüger, Maira Rosin, Sophie Tröger-Görler, Thorsten Heinekamp, Axel A. Brakhage

Biological membranes are laterally heterogeneous and contain specialized microdomains called lipid rafts. Lipid rafts serve as organizational platforms that cluster signaling molecules or modulate membrane protein conformation through their unique lipid environment. There are specific lipid raft marker proteins whose functions remain obscure. One of these proteins is flotillin which has been linked to endocytosis. Here, we investigated the regulation and function of FloA, the sole flotillin homolog in the model fungus Aspergillus nidulans. FloA expression is specifically upregulated in response to calcium stress, which is a regulatory pattern also conserved in Aspergillus fumigatus. BioID proximity labeling revealed that A. nidulans FloA physically interacts with proteins in the endocytic pathway as well as another lipid raft marker, the plasma membrane H⁺-ATPase PmaA. Under calcium stress, PmaA undergoes internalization from the cytoplasmic membrane. However, when floA is deleted, PmaA internalization is prevented, resulting in cell death. This phenotype of the ΔfloA strain could be mimicked by treating the cells with an endocytosis inhibitor during calcium stress. Together, we demonstrate that FloA is essential for the internalization of PmaA during calcium stress, a process that prevents intracellular calcium overload and promotes cell viability. Our results also provide further evidence for flotillin-assisted endocytosis.