Crucial roles of Rab22a in endosomal cargo recycling

Abstract

Endosomal cargo recycling lies at the heart of subcellular trafficking processes under the management of several Ras‐related GTP‐binding proteins (Rabs) which are coordinated by their upstream regulators and require their downstream effectors to display their functions. In this regard, several Rabs have been well‐reviewed except Rab22a. Rab22a is a crucial regulator of vesicle trafficking, early endosome and recycling endosome formation. Notably, recent studies demonstrated the immunological roles of Rab22a, which are closely associated with cancers, infection and autoimmune disorders. This review provides an overview of the regulators and effectors of Rab22a. Also, we highlight the current knowledge of the role of Rab22a in endosomal cargo recycling, including the biogenesis of recycling tubules with the help of a complex with Rab22a at its core, and how different internalized cargo chooses different recycling routes thanks to the cooperation of Rab22a, its effectors and its regulators. Of note, contradictions and speculation related to endosomal cargo recycling that Rab22a brings impacts on are also discussed. Finally, this review endeavors to briefly introduce the various events impacted by Rab22a, particularly focusing on the commandeered Rab22a‐associated endosomal maturation and endosomal cargo recycling, in addition to the extensively investigated oncogenic role of Rab22a.

The Underlying Rab Network of MRGPRX2-Stimulated Secretion Unveils the Impact of Receptor Trafficking on Secretory Granule Biogenesis and Secretion

“…Therefore, their hyperactivation might lead to dynein sequestration, which, by impairing the balance of the bidirectional motility of the SGs, would result in their peripheral accumulation. Both Rab22A and Rab14 play a role in endocytic recycling [ 70 , 71 ] and may impact the recycling of the exocytic machinery. Finally, the Rab27 isoform preference is intriguing.…”