<?xml version="1.0" encoding="UTF-8"?>
<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns="http://purl.org/rss/1.0/" xmlns:dc="http://purl.org/dc/elements/1.1/">
  <channel rdf:about="https://dspace.nii.res.in//https://dspace.nii.res.in/handle/123456789/48">
    <title>DSpace Community: Principal Investigator- Dr. Prafullakumar Tailor</title>
    <link>https://dspace.nii.res.in//https://dspace.nii.res.in/handle/123456789/48</link>
    <description>Principal Investigator- Dr. Prafullakumar Tailor</description>
    <items>
      <rdf:Seq>
        <rdf:li rdf:resource="https://dspace.nii.res.in//https://dspace.nii.res.in/handle/123456789/1349" />
      </rdf:Seq>
    </items>
    <dc:date>2026-04-27T15:41:23Z</dc:date>
  </channel>
  <item rdf:about="https://dspace.nii.res.in//https://dspace.nii.res.in/handle/123456789/1349">
    <title>Cutting Edge: ACVRL1 Signaling Augments CD8a+ Dendritic Cell Development</title>
    <link>https://dspace.nii.res.in//https://dspace.nii.res.in/handle/123456789/1349</link>
    <description>Title: Cutting Edge: ACVRL1 Signaling Augments CD8a+ Dendritic Cell Development
Authors: Tailor, Prafullakumar
Abstract: Dendritic cells (DCs) are a collection of different subtypes, each of which is characterized by specific surface markers, gene-expression patterns, and distinct functions. Members of the IFN regulatory factor family play critical roles in DC development and functions. Recently, Irf8 was shown to activate TGF-β signaling, which led to exacerbated neuroinflammation in the experimental autoimmune encephalomyelitis mouse model. We analyzed the effect of Irf8 on TGF-β/bone morphogenetic protein pathway-specific genes in DCs and identified Acvrl1, a type I TGF-β superfamily receptor, as a gene strongly induced by Irf8 expression. Among various DC subtypes, Acvrl1 is differentially expressed in CD8α(+) DCs. ACVRL1 signaling augmented Irf8-directed classical CD8α(+) DC development. Irf8 expression is essential for plasmacytoid DC and CD8α(+) DC development, and this study demonstrates that ACVRL1 signaling plays a pivotal role whereby it suppresses plasmacytoid DC development while enhancing that of CD8α(+) DCs, thus contributing to DC diversity development.</description>
    <dc:date>2016-01-01T00:00:00Z</dc:date>
  </item>
</rdf:RDF>

