File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1182/blood-2005-01-0226
- Scopus: eid_2-s2.0-28844505689
- PMID: 16141354
- WOS: WOS:000233925900032
- Find via
Supplementary
- Citations:
- Appears in Collections:
Article: Presence of bone marrow-derived circulating progenitor endothelial cells in the newly formed lymphatic vessels
Title | Presence of bone marrow-derived circulating progenitor endothelial cells in the newly formed lymphatic vessels |
---|---|
Authors | |
Issue Date | 2005 |
Publisher | American Society of Hematology. The Journal's web site is located at http://bloodjournal.hematologylibrary.org/ |
Citation | Blood, 2005, v. 106 n. 13, p. 4184-4190 How to Cite? |
Abstract | Bone marrow (BM)-derived circulating endothelial precursor cells (CEPCs) have been reported to incorporate into newly formed blood vessels under physiologic and pathologic conditions. However, it is unknown if CEPCs contribute to lymphangiogenesis. Here we show that in a corneal lymphangiogenesis model of irradiated mice reconstituted with enhanced green fluorescent protein (EGFP)-positive donor bone marrow cells, CEPCs are present in the newly formed lymphatic vessels. Depletion of bone marrow cells by irradiation remarkably suppressed lymphangiogenesis in corneas implanted with fibroblast growth factor-2 (FGF-2). Further, transplantation of isolated EGFP-positive/vascular endothelial growth factor receptor-3-positive (EGFP +/VEGFR-3+) or EGFP+/VEGFR-2+ cell populations resulted in incorporation of EGFP+ cells into the newly formed lymphatic vessels. EGFP+/CEPCs were also present in peritumoral lymphatic vessels of a fibrosarcoma. These data suggest that BM-derived CEPCs may play a role in lymphvasculogenesis. © 2005 by The American Society of Hematology. |
Persistent Identifier | http://hdl.handle.net/10722/68039 |
ISSN | 2023 Impact Factor: 21.0 2023 SCImago Journal Rankings: 5.272 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Religa, P | en_HK |
dc.contributor.author | Cao, R | en_HK |
dc.contributor.author | Bjorndahl, M | en_HK |
dc.contributor.author | Zhou, Z | en_HK |
dc.contributor.author | Zhu, Z | en_HK |
dc.contributor.author | Cao, Y | en_HK |
dc.date.accessioned | 2010-09-06T06:00:45Z | - |
dc.date.available | 2010-09-06T06:00:45Z | - |
dc.date.issued | 2005 | en_HK |
dc.identifier.citation | Blood, 2005, v. 106 n. 13, p. 4184-4190 | en_HK |
dc.identifier.issn | 0006-4971 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/68039 | - |
dc.description.abstract | Bone marrow (BM)-derived circulating endothelial precursor cells (CEPCs) have been reported to incorporate into newly formed blood vessels under physiologic and pathologic conditions. However, it is unknown if CEPCs contribute to lymphangiogenesis. Here we show that in a corneal lymphangiogenesis model of irradiated mice reconstituted with enhanced green fluorescent protein (EGFP)-positive donor bone marrow cells, CEPCs are present in the newly formed lymphatic vessels. Depletion of bone marrow cells by irradiation remarkably suppressed lymphangiogenesis in corneas implanted with fibroblast growth factor-2 (FGF-2). Further, transplantation of isolated EGFP-positive/vascular endothelial growth factor receptor-3-positive (EGFP +/VEGFR-3+) or EGFP+/VEGFR-2+ cell populations resulted in incorporation of EGFP+ cells into the newly formed lymphatic vessels. EGFP+/CEPCs were also present in peritumoral lymphatic vessels of a fibrosarcoma. These data suggest that BM-derived CEPCs may play a role in lymphvasculogenesis. © 2005 by The American Society of Hematology. | en_HK |
dc.language | eng | en_HK |
dc.publisher | American Society of Hematology. The Journal's web site is located at http://bloodjournal.hematologylibrary.org/ | en_HK |
dc.relation.ispartof | Blood | en_HK |
dc.subject.mesh | Animals | en_HK |
dc.subject.mesh | Biological Markers | en_HK |
dc.subject.mesh | Bone Marrow Cells - cytology - metabolism | en_HK |
dc.subject.mesh | Cell Differentiation | en_HK |
dc.subject.mesh | Endothelial Cells - cytology - metabolism | en_HK |
dc.subject.mesh | Female | en_HK |
dc.subject.mesh | Glycoproteins - metabolism | en_HK |
dc.subject.mesh | Green Fluorescent Proteins - metabolism | en_HK |
dc.subject.mesh | Leukemia, Lymphoid - metabolism - pathology | en_HK |
dc.subject.mesh | Lymphatic Vessels - cytology - metabolism | en_HK |
dc.subject.mesh | Male | en_HK |
dc.subject.mesh | Mice | en_HK |
dc.subject.mesh | Mice, Inbred C57BL | en_HK |
dc.subject.mesh | Receptors, Vascular Endothelial Growth Factor - genetics - metabolism | en_HK |
dc.subject.mesh | Stem Cells - cytology - metabolism | en_HK |
dc.title | Presence of bone marrow-derived circulating progenitor endothelial cells in the newly formed lymphatic vessels | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0006-4971&volume=106&issue=13&spage=4184&epage=90&date=2005&atitle=Presence+Of+Bone+Marrow-derived+Circulating+Progenitor+Endothelial+Cells+In+The+Newly+Formed+Lymphatic+Vessels | en_HK |
dc.identifier.email | Zhou, Z:zhongjun@hkucc.hku.hk | en_HK |
dc.identifier.authority | Zhou, Z=rp00503 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1182/blood-2005-01-0226 | en_HK |
dc.identifier.pmid | 16141354 | - |
dc.identifier.scopus | eid_2-s2.0-28844505689 | en_HK |
dc.identifier.hkuros | 100105 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-28844505689&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 106 | en_HK |
dc.identifier.issue | 13 | en_HK |
dc.identifier.spage | 4184 | en_HK |
dc.identifier.epage | 4190 | en_HK |
dc.identifier.isi | WOS:000233925900032 | - |
dc.publisher.place | United States | en_HK |
dc.identifier.f1000 | 10191 | - |
dc.identifier.scopusauthorid | Religa, P=6603614167 | en_HK |
dc.identifier.scopusauthorid | Cao, R=7103341338 | en_HK |
dc.identifier.scopusauthorid | Bjorndahl, M=6506759393 | en_HK |
dc.identifier.scopusauthorid | Zhou, Z=8631856300 | en_HK |
dc.identifier.scopusauthorid | Zhu, Z=7404803288 | en_HK |
dc.identifier.scopusauthorid | Cao, Y=7404524342 | en_HK |
dc.identifier.issnl | 0006-4971 | - |