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BrainSci. 2016,6, 15
Somewhatsurprisingly,consideringtheimportanceofastrocyticIL-6inneuroinflammation[2,4,25,26],
wedidnotobservedramaticeffectsofastrocytic IL-6deficiencyoneitherastrocytesormicrogliaat
the timesstudied. This resultmakes itunlikely thatchanges inglial cell reactivityareunderlyingthe
differences inclinical signsbetweenAst-IL-6KOmiceandfloxedmice.Nevertheless,overall staining
andcellmorphologiesare limitedapproaches,andmoredetailedstudiesareneededtoassessother
rolesofglial cells (other thanIL-6productionbyastrocytes) inclinical signsofEAE.Finally, regarding
thenumberofvessels,weobservedadecrease inAst-IL-6KOmice,which is inagreementwithresults
inmiceoverexpressingIL-6,whichshowextensiverevascularization,both inbasal conditions [25,26]
andafter an injury [34], indicativeof a role of IL-6 invasogenesis. Other studies also support the
idea that IL-6promotesvasogenesis [35]. Probably, this is secondary to thenumberand/or typeof
inflammatorycellspresent in thespinalcord, sincenodifferenceswereobservedinmalemice.
The extent of the reductionof IL-6 in astrocytes of theAst-IL-6KOmice invivohasyet to be
determined.However, studiesofculturedastrocytes fromtheAst-IL-6KOmicedemonstrated that the
astrocytesaredeficient in IL-6production. In thesestudies,analysisofculturesupernatantafter24h
ofstimulation(10ng/mLofLPSand10ng/mLof INF-γ) showedthatastrocytes fromfloxedmice
producedapproximately13ng/mLof IL-6,whereasastrocytes fromAst-IL-6KOmiceonlyproduced
2ng/mLIL-6 [17,18]. Regardlessof theextentof theastrocytic IL-6deficiency in theAst-IL-6KOmice,
adelayinonset toclinicalsymptomswasevident infemales, includinglessdemyelinationat20–22dpi
inaccordancewith the lowerclinical scores.However, thiswasa transienteffect, andsometimeafter
20–22dpi, theEAEwassimilar inbothgenotypes (as indicatedbythe lackofsignificantdifferences in
demyelinationat46dpi), indicatingtheastrocytic IL-6no longerplayedarole.
5.Conclusions
Inconclusion,wehaveshownthat lackofastrocytic IL-6 isnotsufficient topreventEAEdisease,
but it is able todelay thediseaseandtoameliorateclinical scoringandthe inflammatorymilieu in
femalemice. These results support the idea that the localCNSproductionof IL-6 is important in
thisdisease. Several interestingquestionsremaintobeaddressed. Forexample,dueto thedelayed
onsetofclinical signsofdisease inAst-IL-6KOfemales, itwillbe important toanalyze indetail the
primingandinflammatory infiltrates in theCNSof femaleandmaleAst-IL-6KOmiceandtheirfloxed
controls. Furthermore, studiesofmalesat laterdpimayrevealgenotypicdifferencesat laterstages.
Moreover,acomparison of the immunizedAst-IL-6 KO andfloxedmicewith aCFA immunized
control groupcould reveal specificEAEeffects inAst-ILK-6KOmice. Future studieswill address
theseandotherrelevant issuesrelative to theroleofastrocytic IL-6 in theEAE.
Acknowledgments: This work was supported by SAF2011-23272 and SFA2014-56546-R to Juan Hidalgo.
MariaErtagratefullyacknowledgesaPhDfellowshipfromUniversitatAutònomadeBarcelona.
AuthorContributions:M.E.,M.G.,S.J.,A.M.andG.C.were involvedinseveralaspectsof theexperimentscarried
out.M.E. ledmostof theexperimentalwork. J.H.conceivedof theexperiments.M.E.andJ.H.wrote thepaper.
Conflictsof Interest:Theauthorsdeclarenoconflictof interest. The foundingsponsorshadnorole in thedesign
of the study; in the collection, analyses or interpretationofdata; in thewritingof themanuscript; nor in the
decisiontopublish theresults.
References
1. Hirano,T.;Taga,T.;Nakano,N.;Yasukawa,K.;Kashiwamura,S.; Shimizu,K.;Nakajima,K.;Pyun,K.H.;
Kishimoto,T.Purification tohomogeneityandcharacterizationofhumanB-celldifferentiation factor (BCDF
orBSFp-2).Proc.Natl. Acad. Sci.USA1985,82, 5490–5494. [CrossRef] [PubMed]
2. Gruol,D.L.;Nelson,T.E.Physiologicalandpathological rolesof interleukin-6 in thecentralnervoussystem.
Mol.Neurobiol. 1997,15, 307–339. [CrossRef] [PubMed]
3. Schöbitz, B.; deKloet, E.R.; Sutanto,W.; Holsboer, F. Cellular localization of interleukin 6mRNAand
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Buch Advances in Neuroimmunology"
Advances in Neuroimmunology
- Titel
- Advances in Neuroimmunology
- Autor
- Donna Gruol
- Herausgeber
- MDPI
- Ort
- Basel
- Datum
- 2017
- Sprache
- englisch
- Lizenz
- CC BY-NC-ND 4.0
- ISBN
- 978-3-03842-571-7
- Abmessungen
- 17.0 x 24.0 cm
- Seiten
- 164
- Schlagwörter
- neuroimmune, cytokine, chemokine, glia cel, neuron, neurodevelopment, neuroimmune disorder, neurologic disease, psychiatric disease, neuronal injury
- Kategorie
- Medizin