Original title: STING activation drives pericentrosomal positioning of acidic organelles via the VAIL-LRRK2-Rab35 pathway
Shoichi Suenaga, Maria Sakurai, Takeshi Iwatsubo, Tomoki Kuwahara · September 2026
Inside your immune cells, tiny compartments called lysosomes and recycling endosomes help process waste and stress. Scientists wanted to understand how an immune sensor named STING moves these compartments around. They looked at brain immune cells called microglia. When STING is turned on, it triggers a chain reaction that shifts a key protein, LRRK2, to a central spot near the cell center. To move there, LRRK2 relies on internal tracks called microtubules, its own enzymatic activity, a helper target called Rab35, and motor adaptors like JIP4. These helpers gather around the central area too. Finally, a mutation linked to Parkinson disease makes this movement happen even more actively. In short, STING uses LRRK2 to steer cell organelles inward during stress.
Imagine your room has a central table where you keep important items. Normally, you spread things around, but when you get a text from your mom (an immune signal), you start moving all your dirty laundry and recycling bins toward that table. This movement requires a specific worker (LRRK2) and a clear path (microtubules). If that worker has a Parkinson's-linked mutation, they work overtime and move things even faster. In this paper, the immune signal is STING activation, the central table is the pericentrosomal area, and the dirty laundry represents acidic organelles like lysosomes.
This connects the immune system's DNA sensor to how cells organize their internal garbage disposal. For Parkinson's disease, where a common mutation makes LRRK2 hyperactive, the finding suggests immune stress could directly disrupt organelle positioning in brain immune cells, potentially linking infection or inflammation to neurodegeneration.
The abstract does not establish whether this pathway operates in neurons or only in microglia, nor does it show functional consequences of the organelle repositioning for cell health or disease. It also does not test whether the pathway is conserved in human cells or only in model systems.
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STING activation drives pericentrosomal positioning of acidic organelles via the VAIL-LRRK2-Rab35 pathway — Shoichi Suenaga, Maria Sakurai, Takeshi Iwatsubo et al. — bioRxiv — doi:10.64898/2026.09.11.750829
Abstract licence: CC BY
Explanation generated by Synthesis from the abstract — it is not the original paper. This is a preprint, so it hasn't necessarily been peer reviewed.