# Modulation of Peripheral Mast Cell and Brain Microglia Axis via Kinase Inhibition

**Authors:** Xiaoguang Liu, Michaeline Hebron, Kaluvu Balaraman, Louis Ballard, Kimberly Liu, Max Stevenson, Charbel Moussa

PMC · DOI: 10.3390/metabo15030194 · Metabolites · 2025-03-11

## TL;DR

A new drug that inhibits specific enzymes reduces brain cell damage and improves behavior in mice with neurodegenerative diseases.

## Contribution

A novel broad kinase inhibitor (BK40196) is developed and shown to reduce tau pathology and neuroinflammation in mouse models of neurodegeneration.

## Key findings

- BK40196 reduces hyper-phosphorylated tau levels and brain cell loss in neurodegenerative models.
- The drug improves motor, cognitive, and anxiety-related behaviors in treated mice.
- BK40196 limits mast cell activation and reduces microglial activity and brain tryptase levels.

## Abstract

Background/Objectives: Kinase inhibition is a hot therapeutic strategy for several human diseases, including neurodegeneration. Tyrosine kinase c-KIT activates peripheral mast cells, while other kinases including Abelson (c-Abl) promotes autophagy and FYN mediates Tau phosphorylation. We synthesized a novel broad kinase inhibitor (BK40196) and investigated its effects on tau hyper-phosphorylation, cell loss, inflammation and behavior in transgenic rTg4510 and TgAPP (TgSwDI) mice. Methods: Drug synthesis and investigation of the pharmacokinetics and pharmacodynamics effects of BK40196 on behavior, protein levels, mast cells and microglial activity in vivo. Results: We synthesized a novel kinase inhibitor (BK40196) that exhibited high brain penetration and a potentially wide therapeutic dose. BK40196 is a dual c-KIT/c-Abl (Abelson) inhibitor but also displays binding affinity to other kinases, including fused in sarcoma (SRC) and FYN. BK40196 induces autophagy in vitro and limits the maturation of mast cells in vitro and in vivo. BK40196 significantly reduces the levels of hyper-phosphorylated tau and attenuates cell loss, while improving motor, cognitive and behavioral (anxiety) functions in models of neurodegeneration. BK40196 reduces microglial activity and the levels of brain tryptase in parallel with mast cell activation. Conclusions: BK40196 inhibits c-Kit and may play an important role in peripheral and central immunity via mast cells and microglia, respectively, and induces synergistic mechanisms through anti-inflammation and protein clearance that are mutually beneficial to alleviate neurodegenerative pathology. BK40196 is a potential candidate for the treatment of human tauopathies.

## Linked entities

- **Genes:** KIT (KIT proto-oncogene, receptor tyrosine kinase) [NCBI Gene 3815], ABL1 (ABL proto-oncogene 1, non-receptor tyrosine kinase) [NCBI Gene 25], SRC (SRC proto-oncogene, non-receptor tyrosine kinase) [NCBI Gene 6714], FYN (FYN proto-oncogene, Src family tyrosine kinase) [NCBI Gene 2534]
- **Proteins:** MAPT (microtubule associated protein tau), TPSB2 (tryptase beta 2)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** MAPT (microtubule associated protein tau) [NCBI Gene 4137] {aka DDPAC, FTD1, FTDP-17, MAPTL, MSTD, MTBT1}, KIT (KIT proto-oncogene, receptor tyrosine kinase) [NCBI Gene 3815] {aka C-Kit, CD117, MASTC, PBT, SCFR}, FYN (FYN proto-oncogene, Src family tyrosine kinase) [NCBI Gene 2534] {aka SLK, SYN, p59-FYN}, SRC (SRC proto-oncogene, non-receptor tyrosine kinase) [NCBI Gene 6714] {aka ASV, SRC1, THC6, c-SRC, p60-Src}, ABL1 (ABL proto-oncogene 1, non-receptor tyrosine kinase) [NCBI Gene 25] {aka ABL, BCR-ABL, CHDSKM, JTK7, bcr/abl, c-ABL}, FUS (FUS RNA binding protein) [NCBI Gene 2521] {aka ALS6, ETM4, FUS1, HNRNPP2, POMP75, TLS}, TXK (TXK tyrosine kinase) [NCBI Gene 7294] {aka BTKL, PSCTK5, PTK4, RLK, TKL}
- **Diseases:** neurodegeneration (MESH:D019636), inflammation (MESH:D007249), tauopathies (MESH:D024801), anxiety (MESH:D001007)
- **Chemicals:** Abelson (-)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11945821/full.md

## References

60 references — full list in the complete paper: https://tomesphere.com/paper/PMC11945821/full.md

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Source: https://tomesphere.com/paper/PMC11945821