Forskning ved Københavns Universitet - Københavns Universitet

Forside

Ca2+-binding protein NECAB2 facilitates inflammatory pain hypersensitivity

Publikation: Bidrag til tidsskriftReviewForskningfagfællebedømt

  • Ming Dong Zhang
  • Jie Su
  • Csaba Adori
  • Valentina Cinquina
  • Katarzyna Malenczyk
  • Fatima Girach
  • Changgeng Peng
  • Patrik Ernfors
  • Peter Löw
  • Lotta Borgius
  • Kiehn, Ole
  • Masahiko Watanabe
  • Mathias Uhlén
  • Nicholas Mitsios
  • Jan Mulder
  • Tibor Harkany
  • Tomas Hökfelt

Pain signals are transmitted by multisynaptic glutamatergic pathways. Their first synapse between primary nociceptors and excitatory spinal interneurons gates the sensory load. In this pathway, glutamate release is orchestrated by Ca2+-sensor proteins, with N-terminal EF-hand Ca2+-binding protein 2 (NECAB2) being particular abundant. However, neither the importance of NECAB2+ neuronal contingents in dorsal root ganglia (DRGs) and spinal cord nor the function determination by NECAB2 has been defined. A combination of histochemical analyses and single-cell RNA-sequencing showed NECAB2 in small- and medium-sized C- and Aδ D-hair low-threshold mechanoreceptors in DRGs, as well as in protein kinase C γ excitatory spinal interneurons. NECAB2 was downregulated by peripheral nerve injury, leading to the hypothesis that NECAB2 loss of function could limit pain sensation. Indeed, Necab2-/- mice reached a pain-free state significantly faster after peripheral inflammation than did WT littermates. Genetic access to transiently activated neurons revealed that a mediodorsal cohort of NECAB2+ neurons mediates inflammatory pain in the mouse spinal dorsal horn. Here, besides dampening excitatory transmission in spinal interneurons, NECAB2 limited pronociceptive brain-derived neurotrophic factor (BDNF) release from sensory afferents. Hoxb8-dependent reinstatement of NECAB2 expression in Necab2-/- mice then demonstrated that spinal and DRG NECAB2 alone could control inflammation-induced sensory hypersensitivity. Overall, we identify NECAB2 as a critical component of pronociceptive pain signaling, whose inactivation offers substantial pain relief.

OriginalsprogEngelsk
TidsskriftJournal of Clinical Investigation
Vol/bind128
Udgave nummer9
Sider (fra-til)3757-3768
Antal sider12
ISSN0021-9738
DOI
StatusUdgivet - 2018
Eksternt udgivetJa

ID: 202477831