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FEAST: A flow cytometry-based toolkit for interrogating microglial engulfment of synaptic and myelin proteins.
Dissing-Olesen, Lasse; Walker, Alec J; Feng, Qian; Barr, Helena J; Walker, Alicia C; Xie, Lili; Wilton, Daniel K; Das, Indrani; Benowitz, Larry I; Stevens, Beth.
Afiliação
  • Dissing-Olesen L; Department of Neurology, Boston Children's Hospital, F.M. Kirby Neurobiology Center, Boston, MA, 02115, USA.
  • Walker AJ; Harvard Medical School, Boston, MA, 02115, USA.
  • Feng Q; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, 02139, USA.
  • Barr HJ; Department of Neurology, Boston Children's Hospital, F.M. Kirby Neurobiology Center, Boston, MA, 02115, USA.
  • Walker AC; Harvard Medical School, Boston, MA, 02115, USA.
  • Xie L; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, 02139, USA.
  • Wilton DK; Department of Neurosurgery, Boston Children's Hospital, F.M. Kirby Neurobiology Center, Boston, MA, 02115, USA.
  • Das I; Department of Neurology, Boston Children's Hospital, F.M. Kirby Neurobiology Center, Boston, MA, 02115, USA.
  • Benowitz LI; Harvard Medical School, Boston, MA, 02115, USA.
  • Stevens B; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, 02139, USA.
Nat Commun ; 14(1): 6015, 2023 09 27.
Article em En | MEDLINE | ID: mdl-37758703
ABSTRACT
Although engulfment is a hallmark of microglia function, fully validated platforms that facilitate high-throughput quantification of this process are lacking. Here, we present FEAST (Flow cytometric Engulfment Assay for Specific Target proteins), which enables interrogation of in vivo engulfment of synaptic material by brain resident macrophages at single-cell resolution. We optimize FEAST for two different analyses quantification of fluorescent material inside live cells and of engulfed endogenous proteins within fixed cells. To overcome false-positive engulfment signals, we introduce an approach suitable for interrogating engulfment in microglia from perfusion-fixed tissue. As a proof-of-concept for the specificity and versatility of FEAST, we examine the engulfment of synaptic proteins after optic nerve crush and of myelin in two mouse models of demyelination (treatment with cuprizone and injections of lysolecithin). We find that microglia, but not brain-border associated macrophages, engulf in these contexts. Our work underscores how FEAST can be utilized to gain critical insight into functional neuro-immune interactions that shape development, homeostasis, and disease.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Microglia / Proteínas da Mielina Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Microglia / Proteínas da Mielina Idioma: En Ano de publicação: 2023 Tipo de documento: Article