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Merck
  • A pore-forming protein drives macropinocytosis to facilitate toad water maintaining.

A pore-forming protein drives macropinocytosis to facilitate toad water maintaining.

Communications biology (2022-07-23)
Zhong Zhao, Zhi-Hong Shi, Chen-Jun Ye, Yun Zhang
摘要

Maintaining water balance is a real challenge for amphibians in terrestrial environments. Our previous studies with toad Bombina maxima discovered a pore-forming protein and trefoil factor complex βγ-CAT, which is assembled under tight regulation depending on environmental cues. Here we report an unexpected role for βγ-CAT in toad water maintaining. Deletion of toad skin secretions, in which βγ-CAT is a major component, increased animal mortality under hypertonic stress. βγ-CAT was constitutively expressed in toad osmoregulatory organs, which was inducible under the variation of osmotic conditions. The protein induced and participated in macropinocytosis in vivo and in vitro. During extracellular hyperosmosis, βγ-CAT stimulated macropinocytosis to facilitate water import and enhanced exosomes release, which simultaneously regulated aquaporins distribution. Collectively, these findings uncovered that besides membrane integrated aquaporin, a secretory pore-forming protein can facilitate toad water maintaining via macropinocytosis induction and exocytosis modulation, especially in responses to osmotic stress.

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Sigma-Aldrich
渥曼青霉素, Wortmannin, CAS 19545-26-7, is a cell-permeable, potent, selective, and irreversible inhibitor of PI3-Kinase (IC₅₀ = 5 nM). Does not affect any upstream signaling events.
Sigma-Aldrich
抗兔 IgG(全分子)-金 山羊抗, affinity isolated antibody, aqueous glycerol suspension, 10 nm (colloidal gold)
Sigma-Aldrich
抗 小鼠 IgG(全分子)-金 山羊抗, affinity isolated antibody, aqueous glycerol suspension, 5 nm (colloidal gold)