PMID- 17161391 OWN - NLM STAT- MEDLINE DCOM- 20070313 LR - 20181113 IS - 0006-8993 (Print) IS - 0006-8993 (Linking) VI - 1130 IP - 1 DP - 2007 Jan 26 TI - Developmental and injury-induced expression of alpha1beta1 and alpha6beta1 integrins in the rat spinal cord. PG - 54-66 AB - Loss and damage to blood vessels are thought to contribute to secondary tissue loss after spinal cord injury. Integrins might be therapeutic targets to protect the vasculature and/or promote angiogenesis, as their activation can promote tubule formation and survival of endothelial cells in vitro. Here, we show that immunostaining with an antibody against the alpha1beta1 integrin heterodimer is present only in blood vessels from postnatal day 1 (P1) through adulthood in Sprague-Dawley rats. After a spinal cord contusion at T9 in adults, the area of alpha1beta1 integrin positive blood vessels increases within 11 mm from the injury site at 3 days post-injury and remains prominent within the injured core only at 7 days. Staining for the alpha6beta1 integrin heterodimer increases in blood vessels between P10 and adulthood and is present in preganglionic neurons of the intermediolateral cell column (IML) at all ages. The alpha6beta1 integrin is also expressed by motor neurons postnatally, and oligodendrocyte precursors (OPCs), as previously reported. After the contusion, the area of alpha6beta1-stained blood vessels is increased at 3 days and most prominently, 1 mm from the injury site, followed by a significant reduction at 7 days, when alpha6beta1 integrin staining is most prominent around the injured core. Staining is also present in a subset of microglia and/or macrophages. These results raise the possibility that alpha1beta1 and alpha6beta1 integrins in blood vessels might be targeted to reduce blood vessel loss and promote angiogenesis, which may promote tissue sparing after spinal cord injury. FAU - Baker, K Adam AU - Baker KA AD - Kentucky Spinal Cord Injury Research Center, Department of Neurological Surgery, MDR Building, Room 616, University of Louisville, Louisville, KY, USA. FAU - Hagg, Theo AU - Hagg T LA - eng GR - P20 RR015576/RR/NCRR NIH HHS/United States GR - R01 NS045734/NS/NINDS NIH HHS/United States GR - RR15576/RR/NCRR NIH HHS/United States PT - Journal Article PT - Research Support, N.I.H., Extramural PT - Research Support, Non-U.S. Gov't DEP - 20061211 PL - Netherlands TA - Brain Res JT - Brain research JID - 0045503 RN - 0 (Integrin alpha1beta1) RN - 0 (Integrin alpha6beta1) SB - IM MH - Age Factors MH - Animals MH - Blood Vessels/*metabolism MH - Female MH - Integrin alpha1beta1/*metabolism MH - Integrin alpha6beta1/*metabolism MH - Motor Neurons/metabolism MH - Neovascularization, Physiologic/*physiology MH - Oligodendroglia/cytology/metabolism MH - Rats MH - Rats, Sprague-Dawley MH - Spinal Cord/blood supply/cytology/metabolism MH - Spinal Cord Injuries/*metabolism MH - Stem Cells/cytology/metabolism MH - Thoracic Vertebrae MH - Time Factors MH - Wound Healing/physiology PMC - PMC1794000 MID - NIHMS16752 EDAT- 2006/12/13 09:00 MHDA- 2007/03/14 09:00 PMCR- 2008/01/31 CRDT- 2006/12/13 09:00 PHST- 2006/05/24 00:00 [received] PHST- 2006/10/20 00:00 [revised] PHST- 2006/10/26 00:00 [accepted] PHST- 2006/12/13 09:00 [pubmed] PHST- 2007/03/14 09:00 [medline] PHST- 2006/12/13 09:00 [entrez] PHST- 2008/01/31 00:00 [pmc-release] AID - S0006-8993(06)03191-X [pii] AID - 10.1016/j.brainres.2006.10.072 [doi] PST - ppublish SO - Brain Res. 2007 Jan 26;1130(1):54-66. doi: 10.1016/j.brainres.2006.10.072. Epub 2006 Dec 11.