TAM receptors mediate the Fpr2-driven pain resolution and fibrinolysis after nerve injury

Hartmannsberger, B.; Ben-Kraiem, A.; Kramer, S.; Guidolin, C.; Kazerani, I.; Doppler, K.; Thomas, D.; Gurke, R.; Sisignano, M.; Kalelkar, P. P.; Garcia, A.; Monje, P. V.; Nusrat, A.; Brack, A.; Krug, S. M.; Sommer, C.; Rittner, H.

doi:10.1101/2024.08.04.605987

bioRxiv · 10.1101/2024.08.04.605987

TAM receptors mediate the Fpr2-driven pain resolution and fibrinolysis after nerve injury

Hartmannsberger, B.·Ben-Kraiem, A.·Kramer, S.·Guidolin, C.·Kazerani, I.·Doppler, K.·Thomas, D.·Gurke, R.·Sisignano, M.·Kalelkar, P. P.·Garcia, A.·Monje, P. V.·Nusrat, A.·Brack, A.·Krug, S. M.·Sommer, C.·Rittner, H.

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Abstract

Nerve injury causes neuropathic pain and multilevel nerve barrier disruption. Nerve barriers consist of perineurial, endothelial, and myelin barriers. So far, it is unclear whether resealing nerve barriers fosters pain resolution and recovery. To this end, we analysed the nerve barrier property portfolio, pain behaviour battery, and lipidomics for precursors of specialized pro-resolving meditators (SPMs) and their receptors in chronic constriction injury of rat sciatic nerve to identify targets for pain resolution by resealing the selected nerve barriers. Of the three nerve barriers - perineurium, capillaries, and myelin - only capillary tightness specifically against larger molecules, such as fibrinogen, recuperated with pain resolution. Fibrinogen immunoreactivity was not only elevated in rats at the time of neuropathic pain but also in nerve biopsies from patients with (but not without) painful polyneuropathy indicating that sealing of the vascular barrier might be novel approach in pain treatment. 15R-HETE (hydroxyeicosatetraenoic acid), a precursor of aspirin-triggered lipoxin A4, were specifically upregulated at the beginning of pain resolution. Repeated local application of resolvin D1-laden nanoparticles or Fpr2 agonists sex-independently resulted in accelerated pain resolution and fibrinogen removal. Clearing macrophages (Cd206) and fibrinolytic pathways (Plat) were also induced while inflammation (Tnf) and inflammasomes (Nlrp3) were unaffected by this treatment. Blocking TAM receptors (Tyro3, Axl, and Mer) and tyrosine kinase receptors linking haemostasis and inflammation completely inhibited all the effects. In summary, nanoparticles can be used as transporters for fleeting lipids, such as SPMs, and therefore expand the array of possible therapeutic agents. Thus, the Fpr2-Cd206-TAM receptor axis may be a suitable target for strengthening the capillary barrier, removing endoneurial fibrinogen, and boosting pain resolution in patients with chronic neuropathic pain.

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Hartmannsberger, B., Ben-Kraiem, A., Kramer, S., Guidolin, C., Kazerani, I., Doppler, K., Thomas, D., Gurke, R., Sisignano, M., Kalelkar, P. P., Garcia, A., Monje, P. V., Nusrat, A., Brack, A., Krug, S. M., Sommer, C., Rittner, H.. 2024-08-06. TAM receptors mediate the Fpr2-driven pain resolution and fibrinolysis after nerve injury. https://doi.org/10.1101/2024.08.04.605987

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