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Sökning: id:"swepub:oai:DiVA.org:uu-433908" > The Ion Channel and...

  • Hariharan, AshwiniUniv Maryland, Sch Med, Dept Physiol, Baltimore, MD 21201 USA. (författare)

The Ion Channel and GPCR Toolkit of Brain Capillary Pericytes

  • Artikel/kapitelEngelska2020

Förlag, utgivningsår, omfång ...

  • 2020-12-18
  • LAUSANNE, SWITZERLAND :Frontiers Media SA,2020
  • electronicrdacarrier

Nummerbeteckningar

  • LIBRIS-ID:oai:DiVA.org:uu-433908
  • https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-433908URI
  • https://doi.org/10.3389/fncel.2020.601324DOI
  • http://kipublications.ki.se/Default.aspx?queryparsed=id:145569241URI

Kompletterande språkuppgifter

  • Språk:engelska
  • Sammanfattning på:engelska

Ingår i deldatabas

Klassifikation

  • Ämneskategori:ref swepub-contenttype
  • Ämneskategori:for swepub-publicationtype

Anmärkningar

  • Brain pericytes reside on the abluminal surface of capillaries, and their processes cover similar to 90% of the length of the capillary bed. These cells were first described almost 150 years ago (Eberth, 1871; Rouget, 1873) and have been the subject of intense experimental scrutiny in recent years, but their physiological roles remain uncertain and little is known of the complement of signaling elements that they employ to carry out their functions. In this review, we synthesize functional data with single-cell RNAseq screens to explore the ion channel and G protein-coupled receptor (GPCR) toolkit of mesh and thin-strand pericytes of the brain, with the aim of providing a framework for deeper explorations of the molecular mechanisms that govern pericyte physiology. We argue that their complement of channels and receptors ideally positions capillary pericytes to play a central role in adapting blood flow to meet the challenge of satisfying neuronal energy requirements from deep within the capillary bed, by enabling dynamic regulation of their membrane potential to influence the electrical output of the cell. In particular, we outline how genetic and functional evidence suggest an important role for G(s)-coupled GPCRs and ATP-sensitive potassium (K-ATP) channels in this context. We put forth a predictive model for long-range hyperpolarizing electrical signaling from pericytes to upstream arterioles, and detail the TRP and Ca2+ channels and G(q), G(i/o), and G(12/13) signaling processes that counterbalance this. We underscore critical questions that need to be addressed to further advance our understanding of the signaling topology of capillary pericytes, and how this contributes to their physiological roles and their dysfunction in disease.

Ämnesord och genrebeteckningar

Biuppslag (personer, institutioner, konferenser, titlar ...)

  • Weir, NickUniv Maryland, Sch Med, Dept Physiol, Baltimore, MD 21201 USA. (författare)
  • Robertson, ColinUniv Maryland, Sch Med, Dept Physiol, Baltimore, MD 21201 USA. (författare)
  • He, LiqunUppsala universitet,Vaskulärbiologi,Uppsala Univ, Dept Immunol Genet & Pathol, Rudbeck Lab, Uppsala, Sweden.(Swepub:uu)liqhe592 (författare)
  • Betsholtz, ChristerUppsala universitet,Vaskulärbiologi,Science for Life Laboratory, SciLifeLab,Uppsala Univ, Dept Immunol Genet & Pathol, Rudbeck Lab, Uppsala, Sweden.;Karolinska Inst, Dept Med Huddinge MedH, Huddinge, Sweden.;Integrated Cardio Metab Ctr, Huddinge, Sweden.(Swepub:uu)chbet517 (författare)
  • Longden, Thomas A.Univ Maryland, Sch Med, Dept Physiol, Baltimore, MD 21201 USA. (författare)
  • Univ Maryland, Sch Med, Dept Physiol, Baltimore, MD 21201 USA.Vaskulärbiologi (creator_code:org_t)

Sammanhörande titlar

  • Ingår i:Frontiers in Cellular NeuroscienceLAUSANNE, SWITZERLAND : Frontiers Media SA141662-5102

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