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	<title>건강과 대안 &#187; 소포성 수지상 세포</title>
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		<title>[광우병] 수지상 세포를 통한 장으로부터 프리온 단백질의 이동</title>
		<link>http://www.chsc.or.kr/?post_type=reference&#038;p=2269</link>
		<comments>http://www.chsc.or.kr/?post_type=reference&#038;p=2269#comments</comments>
		<pubDate>Wed, 08 Sep 2010 17:55:05 +0000</pubDate>
		<dc:creator>건강과대안</dc:creator>
				<category><![CDATA[광우병]]></category>
		<category><![CDATA[미분류]]></category>
		<category><![CDATA[CJD]]></category>
		<category><![CDATA[dendritic cells]]></category>
		<category><![CDATA[follicular dendritic cells (FDCs)]]></category>
		<category><![CDATA[TSE]]></category>
		<category><![CDATA[vCJD]]></category>
		<category><![CDATA[소포성 수지상 세포]]></category>
		<category><![CDATA[수지상 세포]]></category>
		<category><![CDATA[인간광우병]]></category>

		<guid isPermaLink="false">http://www.chsc.or.kr/?post_type=reference&#038;p=2269</guid>
		<description><![CDATA[광우병, 인간광우병,스크래피 등 전염성 해면상뇌증(TSE)의 원인물질인 병원성 프리온 단백질이 중추신경계로 퍼지기 전에 림프조직에서 복제가 일어나는데&#8230; 내장의 수지상 세포를 통해&#160;장으로부터 프리온 단백질이 이동하는 기전을 규명한&#160;논문입니다.&#160;경구 섭취된 프리온 단백질은 장벽의 [...]]]></description>
				<content:encoded><![CDATA[<p><P>광우병, 인간광우병,스크래피 등 전염성 해면상뇌증(TSE)의 원인물질인 병원성 프리온 단백질이 <BR>중추신경계로 퍼지기 전에 림프조직에서 복제가 일어나는데&#8230; 내장의 수지상 세포를 통해&nbsp;<BR>장으로부터 프리온 단백질이 이동하는 기전을 규명한&nbsp;논문입니다.&nbsp;<BR><BR>경구 섭취된 프리온 단백질은 장벽의 파이어스 패치(peyers patch)를 통해&nbsp;흡수되어 림프계로 전달되고, 림프계 내부에서는 면역세포들의 내포작용(endocytosis)을 통한&nbsp;탐식작용으로 림프절, 비장, 편도선 등으로 세포 이동이 일어나며, 비장에서 케모킨 수용체(chemokine receptor)인 CXCR5가 결핍된 경우 소포성 수지상 세포가 비장과 연결과 연결된 신경에 접근하게 되며, 접근 위치에 도착하고 나면 수지상 세포의 도움을 받아 프리온 단백질이 척수(spinal cord)의 신경축으로 이동하여&nbsp;뇌에 도달하게 됩니다.<BR><A title="The Journal of general virology."><BR></A></P><br />
<H1>Migrating intestinal dendritic cells transport PrP(Sc) from the gut.</H1><br />
<P><A _onclick="return top.js.OpenExtLink(window,event,this)" href="https://mail.google.com/pubmed?term=%22Huang%20FP%22%5BAuthor%5D" target=_blank>Huang FP</A>, <A _onclick="return top.js.OpenExtLink(window,event,this)" href="https://mail.google.com/pubmed?term=%22Farquhar%20CF%22%5BAuthor%5D" target=_blank>Farquhar CF</A>, <A _onclick="return top.js.OpenExtLink(window,event,this)" href="https://mail.google.com/pubmed?term=%22Mabbott%20NA%22%5BAuthor%5D" target=_blank>Mabbott NA</A>, <A _onclick="return top.js.OpenExtLink(window,event,this)" href="https://mail.google.com/pubmed?term=%22Bruce%20ME%22%5BAuthor%5D" target=_blank>Bruce ME</A>, <A _onclick="return top.js.OpenExtLink(window,event,this)" href="https://mail.google.com/pubmed?term=%22MacPherson%20GG%22%5BAuthor%5D" target=_blank><br />
<SCRIPT><!--<br />
D(["mb","MacPherson GG\u003c/a\u003e.\u003c/p\u003e\n\n\u003cp\u003eSir William Dunn School of Pathology, South Parks Road, Oxford OX1 3RE, UK.\u003c/p\u003e\n\u003cp\u003e\u003cfont color\u003d\"#810081\"\u003e출처 : \u003c/font\u003e\u003ca href\u003d\"http://www.ncbi.nlm.nih.gov/pubmed/11752724\" target\u003d\"_blank\" onclick\u003d\"return top.js.OpenExtLink(window,event,this)\"\u003ehttp://www.ncbi.nlm.nih.gov/\u003cWBR\u003epubmed/11752724\u003c/a\u003e\u003c/p\u003e\n\u003cp\u003e\u003d\u003d\u003d\u003d\u003d\u003d\u003d\u003d\u003d\u003d\u003d\u003d\u003d\u003d\u003d\u003d\u003d\u003d\u003d\u003d\u003d\u003c/p\u003e\u003c/div\u003e\n\u003cdiv\u003eRelevance of the regional lymph node in scrapie pathogenesis after peripheral infection of hamsters\u003c/div\u003e\n\u003cdiv\u003eChristine Kratzel,\u003csup\u003e\u003cimg alt\u003d\"corresponding author\" src\u003d\"https://mail.google.com/corehtml/pmc/pmcgifs/corrauth.gif\"\u003e\u003c/sup\u003e\u003csup\u003e\u003cfont size\u003d\"2\"\u003e1\u003c/font\u003e\u003c/sup\u003e Dominique Krüger,\u003csup\u003e\u003cfont size\u003d\"2\"\u003e1\u003c/font\u003e\u003c/sup\u003e and Michael Beekes\u003csup\u003e\u003cimg alt\u003d\"corresponding author\" src\u003d\"https://mail.google.com/corehtml/pmc/pmcgifs/corrauth.gif\"\u003e\u003c/sup\u003e\u003csup\u003e\u003cfont size\u003d\"2\"\u003e1\u003c/font\u003e\u003c/sup\u003e\u003c/div\u003e\n\n\u003cdiv\u003e\u003csup\u003e\u003cfont size\u003d\"2\"\u003e1\u003c/font\u003e\u003c/sup\u003eRobert Koch-Institut, P24 – Transmissible Spongiforme Enzephalopathien Nordufer 20, D-Berlin 13353, Germany\u003c/div\u003e\n\u003cdiv\u003e\u003csup\u003e\u003cimg alt\u003d\"corresponding author\" src\u003d\"https://mail.google.com/corehtml/pmc/pmcgifs/corrauth.gif\"\u003e\u003c/sup\u003eCorresponding author.\u003c/div\u003e\n\u003cdiv\u003e\u003cspan\u003eChristine Kratzel: \u003cspan\u003e\u003ca href\u003d\"mailto:chris.kratzel@web.de\" target\u003d\"_blank\" onclick\u003d\"return top.js.OpenExtLink(window,event,this)\"\u003echris.kratzel@web.de\u003c/a\u003e\u003c/span\u003e\u003cspan\u003e\u003c/span\u003e ; \u003c/span\u003e\u003cspan\u003eDominique Krüger: \u003cspan\u003e\u003ca href\u003d\"mailto:kruegerd@rki.de\" target\u003d\"_blank\" onclick\u003d\"return top.js.OpenExtLink(window,event,this)\"\u003ekruegerd@rki.de\u003c/a\u003e\u003c/span\u003e\u003cspan\u003e\u003c/span\u003e ; \u003c/span\u003e\u003cspan\u003eMichael Beekes: \u003cspan\u003e\u003ca href\u003d\"mailto:beekesm@rki.de\" target\u003d\"_blank\" onclick\u003d\"return top.js.OpenExtLink(window,event,this)\"\u003ebeekesm@rki.de\u003c/a\u003e\u003c/span\u003e\u003cspan\u003e\u003c/span\u003e \u003c/span\u003e\u003c/div\u003e\n\n\u003cdiv\u003e \u003c/div\u003e\n\u003cdiv\u003e출처 : \u003cspan\u003eBMC Vet Res. \u003c/span\u003e\u003cspan\u003e2007; \u003c/span\u003e\u003cspan\u003e3\u003c/span\u003e\u003cspan\u003e\u003c/span\u003e\u003cspan\u003e: 22. \u003c/span\u003e\n\u003cdiv\u003e\u003cspan\u003ePublished online 2007 September 25. \u003c/span\u003e\u003cspan\u003e\u003c/span\u003e\u003cspan\u003edoi: \u003ca href\u003d\"http://dx.crossref.org/10.1186%2F1746-6148-3-22\" target\u003d\"_blank\" onclick\u003d\"return top.js.OpenExtLink(window,event,this)\"\u003e10.1186/1746-6148-3-22",1]<br />
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MacPherson GG</A>.</P><br />
<P>Sir William Dunn School of Pathology, South Parks Road, Oxford OX1 3RE, UK.</P><br />
<P><FONT color=#810081>출처 : </FONT><FONT color=#000000>J Gen Virol. 2002 Jan;83(Pt 1):267-71.</FONT><BR><A _onclick="return top.js.OpenExtLink(window,event,this)" href="http://www.ncbi.nlm.nih.gov/pubmed/11752724" target=_blank>http://www.ncbi.nlm.nih.gov/<WBR>pubmed/11752724</A><BR><BR></P><br />
<H3 class=abstract_label>Abstract</H3><br />
<P>Bovine spongiform encephalopathy, variant Creutzfeldt-Jakob disease (vCJD) and possibly also sheep scrapie are orally acquired transmissible spongiform encephalopathies (TSEs). TSE agents usually replicate in lymphoid tissues before they spread into the central nervous system. In mouse TSE models PrP(c)-expressing follicular dendritic cells (FDCs) resident in lymphoid germinal centres are essential for replication, and in their absence neuroinvasion is impaired. Disease-associated forms of PrP (PrP(Sc)), a biochemical marker for TSE infection, also accumulate on FDCs in the lymphoid tissues of patients with vCJD and sheep with natural scrapie. TSE transport mechanisms between gut lumen and germinal centres are unknown. Migratory bone marrow-derived dendritic cells (DCs), entering the intestinal wall from blood, sample antigens from the gut lumen and carry them to mesenteric lymph nodes. Here we show that DCs acquire PrP(Sc) in vitro, and transport intestinally administered PrP(Sc) directly into lymphoid tissues in vivo. These studies suggest that DCs are a cellular bridge between the gut lumen and the lymphoid TSE replicative machinery.</P></p>
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		<title>[광우병] 젊은 사람이 나이 든 사람보다 광우병에 취약한 이유?</title>
		<link>http://www.chsc.or.kr/?post_type=reference&#038;p=1180</link>
		<comments>http://www.chsc.or.kr/?post_type=reference&#038;p=1180#comments</comments>
		<pubDate>Fri, 16 Oct 2009 21:58:39 +0000</pubDate>
		<dc:creator>건강과대안</dc:creator>
				<category><![CDATA[광우병]]></category>
		<category><![CDATA[식품 · 의약품]]></category>
		<category><![CDATA[follicular dendritic cells]]></category>
		<category><![CDATA[면역계]]></category>
		<category><![CDATA[소포성 수지상 세포]]></category>
		<category><![CDATA[인간광우병]]></category>
		<category><![CDATA[프리온]]></category>

		<guid isPermaLink="false">http://www.chsc.or.kr/?post_type=reference&#038;p=1180</guid>
		<description><![CDATA[젊은 사람들이 나이든 사람들에 비해 인간광우병에 민감한 이유를 밝히려는 과학자들의 연구가 계속되고 있는 가운데&#8230; 로슬린 연구소의 과학자들은 쥐 실험을 통해 프리온 단백질과 면역계의 상호작용에 대한 연구결과를 발표했습니다.변형 프리온은 [...]]]></description>
				<content:encoded><![CDATA[<p>젊은 사람들이 나이든 사람들에 비해 인간광우병에 민감한 이유를 밝히려는 과학자들의 연구가 계속되고 있는 가운데&#8230; 로슬린 연구소의 과학자들은 쥐 실험을 통해 프리온 단백질과 면역계의 상호작용에 대한 연구결과를 발표했습니다.<BR><BR>변형 프리온은 중추신경계로 퍼지기 전에 비장, 림파구, 편도 등 면역계의 일부인 림프조직에 축적되는데, Neil Mabbott를 비롯한 로슬린 연구소의 학자들은 프리온은 필수불가결하게 면역계의 특별한 세포인 소포성 수지상 세포 (follicular dendritic cells)를&nbsp; &#8220;납치(hijack)&#8221;하는 것을 확인했습니다.(변형 프리온 단백질이 소포성 수지상 세포와 반드시 결합하여 그 세포에서 축적되고 복제됩니다)<BR><BR>그러나 나이 든 쥐에서는 소포성 수지상 세포가 손상된(감소된) 것이 확인됐습니다.<BR><BR>광우병과 소포성 수지상 세포 (follicular dendritic cells)의 연관성은 예전에 [네이처]에도 발표된 바가 있습니다.<BR><BR>에든베러 대학의 로슬린 연구소 연구팀은 이번 연구결과가 인간광우병 예방백신 개발에 도움이될 것으로 판단하고 있다고 합니다.<BR><BR>==========================================================<BR><BR><br />
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<H1>Cells link to CJD in young people </H1></DIV></TD></TR><br />
<TR><br />
<TD class=storybody><!-- S BO --><!-- S IIMA --><br />
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<DIV><IMG height=170 alt="Human brain of someone infected with vCJD" hspace=0 src="http://newsimg.bbc.co.uk/media/images/46549000/jpg/_46549190__45806856_vcjd-1.jpg" width=226 border=0><br />
<DIV class=cap>There have been more than 160 definite or probable UK cases of vCJD</DIV></DIV></TD></TR></TBODY></TABLE><!-- E IIMA --><!-- S SF --><br />
<P class=first><STRONG>출처 : BBC&nbsp;</STRONG><SPAN class=lu>Page last updated at </SPAN>15:49 GMT, Thursday, 15 October 2009 16:49 UK<BR><BR><STRONG>Cells in the immune system could hold the key to why younger people are more susceptible to the human form of mad cow disease, scientists have said.</STRONG><br />
<P>Patients diagnosed with variant CJD are just 28 years old on average. It has been unclear why older people have not been affected to the same extent. </P><br />
<P>Now older cells, by working less efficiently than they used to due to age, are thought to hamper the disease. </P><br />
<P>Edinburgh University scientists said it could help with vaccine development. </P><!-- E SF --><br />
<P>The researches behind the study believe the findings could also improve the diagnosis of vCJD. </P><br />
<P><B>Nervous system</B></P><br />
<P>Analysing mice, researchers at the university&#8217;s Roslin Institute looked at how the immune system interacts with corrupted proteins, known as prions, which are linked to vCJD. </P><br />
<P>Prions accumulate in lymphoid tissues, part of the body&#8217;s immune system which include the spleen, lymph nodes and tonsils, before spreading to the central nervous system, where they kill off brain cells and cause neurological disease. </P><br />
<P>The researchers found that the prions essentially &#8220;hijack&#8221; specific cells in the immune system, known as follicular dendritic cells. </P><br />
<P>The prions accumulate and replicate on the cells, until they reach a sufficient level to spread to the nerves and the brain.</P><!-- S IBOX --><br />
<TABLE cellSpacing=0 cellPadding=0 width=231 align=right border=0><br />
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<TD width=5><IMG height=1 alt="" hspace=0 src="http://newsimg.bbc.co.uk/shared/img/o.gif" width=5 border=0></TD><br />
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<DIV><br />
<DIV class=mva><IMG height=13 alt="" src="http://newsimg.bbc.co.uk/nol/shared/img/v3/start_quote_rb.gif" width=24 border=0> <B>It has always been unclear why younger people were more susceptible to variant CJD and the assumption that they were more likely to eat cheap meat products is far too simplistic</B> <IMG height=13 alt="" src="http://newsimg.bbc.co.uk/nol/shared/img/v3/end_quote_rb.gif" width=23 align=right border=0><BR clear=all></DIV></DIV><br />
<DIV class=mva><br />
<DIV>Dr Neil Mabbott<BR>The Roslin Institute</DIV></DIV></TD></TR></TBODY></TABLE><!-- E IBOX --><br />
<P>But the study, funded by the Biotechnology and Biological Sciences Research Council, found that those cells were impaired in older mice. </P><br />
<P>As a result, they were unable to trap and replicate the corrupted proteins and the mice did not develop clinical disease. </P><br />
<P>Researchers said their study could explain why vCJD does not affect older humans to the same extent and why it occurs almost exclusively in young people. </P><br />
<P>Dr Neil Mabbott, of The Roslin Institute, said: &#8220;It has always been unclear why younger people were more susceptible to variant CJD and the assumption that they were more likely to eat cheap meat products is far too simplistic. </P><br />
<P>&#8220;Understanding what happens to these cells, which are important for the body&#8217;s immune responses, could help us develop better ways of diagnosing variant CJD or even find ways of preventing prions from spreading to the brain. It could also help to create a vaccine.&#8221; </P><br />
<P>The findings are published in the Journal of Immunology. </P></TD></TR></TBODY></TABLE></p>
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