Histopathological Investigation of Different MCAO Modalities and Impact of Autologous Bone Marrow Mononuclear Cell Administration in an Ovine Stroke Model

被引:15
作者
Boltze, Johannes [1 ,2 ]
Nitzsche, Bjoern [1 ,2 ,3 ]
Geiger, Kathrin D. [4 ]
Schoon, Heinz-Adolf [3 ]
机构
[1] Fraunhofer Inst Cell Therapy & Immunol, D-04103 Leipzig, Germany
[2] Univ Leipzig, Translat Ctr Regenerat Med, D-04103 Leipzig, Germany
[3] Univ Leipzig, Fac Vet Med, Inst Pathol, D-04103 Leipzig, Germany
[4] Tech Univ Dresden, Med Fac Carl Gustav Carus, Inst Pathol, Dept Neuropathol, D-01307 Dresden, Germany
关键词
Stroke; Brain ischaemia; Large animal model; Cell therapy; Neuroprotection; Translational research; CEREBRAL-ARTERY OCCLUSION; ACUTE ISCHEMIC-STROKE; NEURAL STEM-CELLS; CANINE MODEL; WHITE-MATTER; TPA THERAPY; THROMBOLYSIS; INFLAMMATION; COLLAGEN; INFARCT;
D O I
10.1007/s12975-011-0101-5
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Translational researchers and clinicians recommend the use of large animal models in preclinical stroke research. This represents an important part of a strategy aiming to prevent past translational failures in future therapeutic developments. Thirty-five Merino rams were subjected to sham surgery (n=3), one-branch middle cerebral artery occlusion (MCAO, n=8) or total MCAO (n=24). Twelve animals from the latter group received intravenous administration of 4x10(6) autologous mononuclear bone marrow cells (BM MNC) per kilogram 24 h after total MCAO. Animals were sacrificed at day 49 post MCAO. Histological investigations were performed to reveal (1) the impact of different MCAO modalities on a cellular level and (2) the influence of BM MNC therapy following stroke. Clear differences between one-branch and total MCAO were observed histologically with results being comparable to those seen in human patients. BM MNC treatment reduced final lesion extension, lymphocytic infiltration and axonal degeneration after MCAO. The sheep model may represent a feasible tool for translational stroke research as pathohistological findings mimic the situation in humans. Histological evidence was found for beneficial impact of autologous BM MNC therapy. Further studies are needed to assess the neurofunctional impact of the approach in the gyrencephalic brain.
引用
收藏
页码:279 / 293
页数:15
相关论文
共 52 条
[1]  
Abramoff M.D., 2004, Biophotonics International, V11, P36
[2]   Human neural stem cells enhance structural plasticity and axonal transport in the ischaemic brain [J].
Andres, Robert H. ;
Horie, Nobutaka ;
Slikker, William ;
Keren-Gill, Hadar ;
Zhan, Ke ;
Sun, Guohua ;
Manley, Nathan C. ;
Pereira, Marta P. ;
Sheikh, Lamiya A. ;
McMillan, Erin L. ;
Schaar, Bruce T. ;
Svendsen, Clive N. ;
Bliss, Tonya M. ;
Steinberg, Gary K. .
BRAIN, 2011, 134 :1777-1789
[3]   Brain protection using autologous bone marrow cell, metalloproteinase inhibitors, and metabolic treatment in cerebral ischemia [J].
Baker, Andrew H. ;
Sica, Vincenzo ;
Work, Lorraine M. ;
Williams-Ignarro, Sharon ;
de Nigris, Filomena ;
Lerman, Lilach O. ;
Casamassimi, Amelia ;
Lanza, Alessandro ;
Schiano, Concetta ;
Rienzo, Monica ;
Ignarro, Louis J. ;
Napoli, Claudio .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (09) :3597-3602
[4]   Why are stroke patients excluded from TPA therapy? An analysis of patient eligibility [J].
Barber, PA ;
Zhang, J ;
Demchuk, AM ;
Hill, MD ;
Buchan, AM .
NEUROLOGY, 2001, 56 (08) :1015-1020
[5]  
Battistella V, 2011, REGEN MED, V6, P45, DOI [10.2217/rme.10.97, 10.2217/RME.10.97]
[6]  
Bock P., 1989, ROMEIS MIKROSKOPISCH
[7]   Permanent middle cerebral artery occlusion in sheep: a novel large animal model of focal cerebral ischemia [J].
Boltze, Johannes ;
Foerschler, Annette ;
Nitzsche, Bjoern ;
Waldmin, Daniela ;
Hoffmann, Anke ;
Boltze, Christiane M. ;
Dreyer, Antje Y. ;
Goldammer, Axel ;
Reischauer, Anne ;
Haertig, Wolfgang ;
Geiger, Kathrin D. ;
Barthel, Henryk ;
Emmrich, Frank ;
Gille, Uwe .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2008, 28 (12) :1951-1964
[8]   Mechanisms contributing to cerebral infarct size after stroke: gender, reperfusion, T lymphocytes, and Nox2-derived superoxide [J].
Brait, Vanessa H. ;
Jackman, Katherine A. ;
Walduck, Anna K. ;
Selemidis, Stavros ;
Diep, Henry ;
Mast, Anja E. ;
Guida, Elizabeth ;
Broughton, Brad R. S. ;
Drummond, Grant R. ;
Sobey, Christopher G. .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2010, 30 (07) :1306-1317
[9]   Autologous bone marrow mononuclear cells enhance recovery after acute ischemic stroke in young and middle-aged rats [J].
Brenneman, Miranda ;
Sharma, Sushil ;
Harting, Matthew ;
Strong, Roger ;
Cox, Charles S., Jr. ;
Aronowski, Jarek ;
Grotta, James C. ;
Savitz, Sean I. .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2010, 30 (01) :140-149
[10]   Intracranial artery calcification: A newly identified risk factor of ischemic stroke [J].
Chen, Xiang-yan ;
Lam, Wynnie Wai Man ;
Ng, Ho Keung ;
Fan, Yu-Hua ;
Wong, Ka Sing .
JOURNAL OF NEUROIMAGING, 2007, 17 (04) :300-303