Researchers at the University of Tokyo have shed light on the molecular mechanisms underlying SLC29A3 disorders

The researchers have shown how histiocytosis in SLC29A3 disorders is driven by TLR7/8 stress responses.

In humans, the SLC29A3 gene regulates the function of lysosomes to control waste recycling in cells such as macrophages (that engulf and destroy foreign bodies).

This gene encodes for the lysosomal protein that transports nucleosides – degradation products of RNA and DNA – from lysosomes to the cytoplasm.  

Loss-of-function mutations in the SLC29A3 gene lead to aberrant nucleoside storage, resulting in a spectrum of conditions called SLC29A3 disorders.

These disorders can manifest in the form of pigmented skin patches, enlargement of the liver/ spleen, hearing loss, or type 1 diabetes.

A key manifestation of this group of disorders is histiocytosis, which is characterised by the accumulation of mononuclear phagocytes (histiocytes) in multiple organs.

However, the molecular link between lysosomal nucleoside storage and histiocytosis has remained elusive so far, making the treatment of this condition challenging.



Establish the mechanism


A team of Japanese researchers has now been able to solve this mystery and establish the mechanism underlying SLC29A3 disorders.

The findings clearly describe how the aberrant responses of toll-like receptor (TLR) 7 and TLR8 – immune proteins expressed on macrophages – drive histiocytosis under conditions of SLC29A3 loss-of-function.

Professor Kensuke Miyake, from The Institute of Medical Science, The University of Tokyo and the corresponding author of the article said: “We have now uncovered how TLR signalling, a key innate immune response pathway, contributes to histiocytosis in SLC29A3 disorders.”

Pathogens engulfed by macrophages are broken down within the lysosomes.

The degradation of pathogenic RNA leads to the generation of nucleosides, which can be sensed by TLR7 and TLR8.

Given that SLC29A3 mutations lead to abnormal nucleoside storage within lysosomes, the authors hypothesised that the constitutive activation of TLR7 and TLR8 by nucleosides would be involved in SLC29A3 disorders.

They tested this hypothesis in mice lacking this gene.

While Slc29a3–/– mice showed significant nucleoside accumulation and histiocytosis, the latter phenotype disappeared when the TLR7 gene was knocked out (ie, in Slc29a3–/– Tlr7–/– mice).

This demonstrated that the histiocytosis occurring due to SLC29A3 mutations was dependent on TLR7.

The results also showed that in Slc29a3–/– mice, during excess lysosomal nucleoside storage, TLR7 promoted the proliferation and maturation of a subset of macrophages.


Patient-derived monocytes


Similar findings were observed in patient-derived monocytes with a SLC29A3 mutation.

These monocytes showed greater survival and proliferation after stimulation with macrophage colony stimulating factor (M-CSF), a macrophage survival factor, than monocytes derived from healthy subjects.

Interestingly, this enhanced survival and proliferation was attenuated when TLR8 was inhibited; human monocytes use TLR8 rather than TLR7 to respond to nucleosides. 

Associate Professor Takuma Shibata, who is also the lead author on this study, explained: “To put it simply, mutations in SLC29A3 lead to nucleoside accumulation in macrophages.

“These nucleosides activate TLR7 and TLR8, and this excessive TLR response leads to excess macrophage proliferation and accumulation.”

Miyake added: “In a way, our findings show that SLC29A3 acts as a negative regulator of the TLR7/8 response in cells of the innate immune system.” 

The study by the group led by Miyake and Shibata answers a long-standing question in the field of innate immunology.

Miyake concluded: “TLR7 and TLR8 could serve as therapeutic targets for SLC29A3 disorders, and this is very promising from the perspective of developing novel therapeutic interventions for these conditions.

“Moreover, the findings can also pave the way for understanding the pathogenic mechanisms of other disorders associated with macrophage proliferation and accumulation.” 

The study is published in the Journal of Experimental Medicine.

Image: An abnormal response of pathogen sensors in macrophages causes histiocytosis by driving macrophage proliferation. Credit: Takuma Shibata, Ryota Sato, Masato Taoka, Shin-Ichiroh Saitoh, Mayumi Komine, Kiyoshi Yamaguchi, Susumu Goyama, Yuji Motoi, Jiro Kitaura, Kumi Izawa, Yoshio Yamauchi, Yumiko Tsukamoto, Takeshi Ichinohe, Etsuko Fujita, Ryosuke Hiranuma, Ryutaro Fukui, Yoichi Furukawa, Toshio Kitamura, Toshiyuki Takai, Arinobu Tojo, Mamitaro Ohtsuki, Umeharu Ohto, Toshiyuki Shimizu, Manabu Ozawa, Nobuaki Yoshida, Toshiaki Isobe, Eicke Latz, Kojiro Mukai, Tomohiko Taguchi, Kensuke Miyake.

Research Aether / Health Uncovered