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Myelin down-regulates myelin phagocytosis by microglia and macrophages through interactions between CD47 on myelin and SIRPalpha (signal regulatory protein-alpha) on phagocytes
Hebrew University Hadassah Medical School, Jerusalem.
Hebrew University Hadassah Medical School, Jerusalem.
Umeå universitet, Medicinska fakulteten, Institutionen för integrativ medicinsk biologi (IMB), Histologi med cellbiologi.
Hebrew University Hadassah Medical School, Jerusalem.
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2011 (Engelska)Ingår i: Journal of Neuroinflammation, ISSN 1742-2094, E-ISSN 1742-2094, Vol. 8, nr 1, s. 24-Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

BACKGROUND: Traumatic injury to axons produces breakdown of axons and myelin at the site of the lesion and then further distal to this where Wallerian degeneration develops. The rapid removal of degenerated myelin by phagocytosis is advantageous for repair since molecules in myelin impede regeneration of severed axons. Thus, revealing mechanisms that regulate myelin phagocytosis by macrophages and microglia is important. We hypothesize that myelin regulates its own phagocytosis by simultaneous activation and down-regulation of microglial and macrophage responses. Activation follows myelin binding to receptors that mediate its phagocytosis (e.g. complement receptor-3), which has been previously studied. Down-regulation, which we test here, follows binding of myelin CD47 to the immune inhibitory receptor SIRPalpha (signal regulatory protein-alpha) on macrophages and microglia.

METHODS: CD47 and SIRPalpha expression was studied by confocal immunofluorescence microscopy, and myelin phagocytosis by ELISA.

RESULTS: We first document that myelin, oligodendrocytes and Schwann cells express CD47 without SIRPalpha and further confirm that microglia and macrophages express both CD47 and SIRPalpha. Thus, CD47 on myelin can bind to and subsequently activate SIRPalpha on phagocytes, a prerequisite for CD47/SIRPalpha-dependent down-regulation of CD47+/+ myelin phagocytosis by itself. We then demonstrate that phagocytosis of CD47+/+ myelin is augmented when binding between myelin CD47 and SIRPalpha on phagocytes is blocked by mAbs against CD47 and SIRPalpha, indicating that down-regulation of phagocytosis indeed depends on CD47-SIRPalpha binding. Further, phagocytosis in serum-free medium of CD47+/+ myelin is augmented after knocking down SIRPalpha levels (SIRPalpha-KD) in phagocytes by lentiviral infection with SIRPalpha-shRNA, whereas phagocytosis of myelin that lacks CD47 (CD47-/-) is not. Thus, myelin CD47 produces SIRPalpha-dependent down-regulation of CD47+/+ myelin phagocytosis in phagocytes. Unexpectedly, phagocytosis of CD47-/- myelin by SIRPalpha-KD phagocytes, which is not altered from normal when tested in serum-free medium, is augmented when serum is present. Therefore, both myelin CD47 and serum may each promote SIRPalpha-dependent down-regulation of myelin phagocytosis irrespective of the other.

CONCLUSIONS: Myelin down-regulates its own phagocytosis through CD47-SIRPalpha interactions. It may further be argued that CD47 functions normally as a marker of "self" that helps protect intact myelin and myelin-forming oligodendrocytes and Schwann cells from activated microglia and macrophages. However, the very same mechanism that impedes phagocytosis may turn disadvantageous when rapid clearance of degenerated myelin is helpful.

Ort, förlag, år, upplaga, sidor
2011. Vol. 8, nr 1, s. 24-
Nyckelord [en]
peripheral nervous-system; membrane attack complex; necrosis-factor-alpha; wallerian degeneration; schwann-cells; spinal-cord; scavenger-receptor; in-vitro; injury; demyelination
Nationell ämneskategori
Medicinska och farmaceutiska grundvetenskaper
Identifikatorer
URN: urn:nbn:se:umu:diva-41357DOI: 10.1186/1742-2094-8-24PubMedID: 21401967OAI: oai:DiVA.org:umu-41357DiVA, id: diva2:405683
Tillgänglig från: 2011-03-23 Skapad: 2011-03-23 Senast uppdaterad: 2018-06-08Bibliografiskt granskad

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