DAPI Diffusion After Intravitreal Injection of Mesenchymal Stem Cells in the Injured Retina of Rats

被引:33
作者
Castanheira, Paula [1 ]
Torquetti, Leonardo Torquetti [2 ]
Soares Magalhas, Debora Rodrigues [1 ]
Nehemy, Marcio B. [2 ]
Goes, Alfredo M. [1 ]
机构
[1] Univ Fed Minas Gerais, Dept Biochem & Immunol, Inst Biol Sci, BR-31270901 Belo Horizonte, MG, Brazil
[2] Univ Fed Minas Gerais, Dept Ophthalmol, Fac Med, Sao Geraldo Eye Hosp, BR-31270901 Belo Horizonte, MG, Brazil
关键词
Mesenchymal stem cells; Stem cell-based therapy; Retinal damage; Retinal regeneration; DAPI; Quantum dot; MARROW STROMAL CELLS; BONE-MARROW; IN-VIVO; MYOCARDIAL-INFARCTION; PROGENITOR CELLS; DIFFERENTIATION; BRAIN; TRANSPLANTATION; ENGRAFTMENT; SURVIVAL;
D O I
10.3727/096368909788809811
中图分类号
Q813 [细胞工程];
学科分类号
摘要
To evaluate DAPI (4',6-diamidino-2-phenylindole) as a nuclear tracer of stem cell migration and incorporation it was observed the pattern of retinal integration and differentiation of mesenchymal stem cells (MSCs) injected into the vitreous cavity of rat eyes with retinal injury, For this purpose adult rat retinas were submitted to laser damage followed by transplantation of DAPI-labeled BM-MSCs grafts and double-labeled DAPI and quantum dot-labeled BM-MSCs. To assess a possible DAPI diffusion as well its the integration and differentiation of DAPI-labeled BM-MSCs in laser-injured retina, host retinas were evaluated 8 weeks after injury/transplantation. It was demonstrated that. 8 weeks after the transplant, most of the retinal cells in all neural retinal presented nuclear DAPI labeling, specifically in the outer nuclear layer (ONL), inner nuclear layer (INL), and ganglion cell layer (GCL). Meanwhile, at this point, most of the double-labeled BM-MSCs (DAPI and quantum dot) remained in the vitreous cavity and no retinal cells presented the quantum dot marker. Based on these evidences we concluded that DAPI diffused to adjacent retinal cells while the nanocrystals remained labeling only the transplanted BM-MSCs. Therefore, DAPI is not a useful marker for stem cells in vivo tracing experiments because the DAPI released from dying cells in moment of the transplant are taken tip by host cells in the tissue.
引用
收藏
页码:423 / 431
页数:9
相关论文
共 35 条
[1]   Efficient magnetic cell labeling with protamine sulfate complexed to ferumoxides for cellular MRI [J].
Arbab, AS ;
Yocum, GT ;
Kalish, H ;
Jordan, EK ;
Anderson, SA ;
Khakoo, AY ;
Read, EJ ;
Frank, JA .
BLOOD, 2004, 104 (04) :1217-1223
[2]   From marrow to brain: Expression of neuronal phenotypes in adult mice [J].
Brazelton, TR ;
Rossi, FMV ;
Keshet, GI ;
Blau, HM .
SCIENCE, 2000, 290 (5497) :1775-1779
[3]   Muscle regeneration by bone marrow derived myogenic progenitors [J].
Ferrari, G ;
Cusella-De Angelis, G ;
Coletta, M ;
Paolucci, E ;
Stornaiuolo, A ;
Cossu, G ;
Mavilio, F .
SCIENCE, 1998, 279 (5356) :1528-1530
[4]   Engraftable human neural stem cells respond to developmental cues, replace neurons, and express foreign genes [J].
Flax, JD ;
Aurora, S ;
Yang, CH ;
Simonin, C ;
Wills, AM ;
Billinghurst, LL ;
Jendoubi, M ;
Sidman, RL ;
Wolfe, JH ;
Kim, SU ;
Snyder, EY .
NATURE BIOTECHNOLOGY, 1998, 16 (11) :1033-1039
[5]   SURVIVAL AND DIFFERENTIATION OF ADULT NEURONAL PROGENITOR CELLS TRANSPLANTED TO THE ADULT BRAIN [J].
GAGE, FH ;
COATES, PW ;
PALMER, TD ;
KUHN, HG ;
FISHER, LJ ;
SUHONEN, JO ;
PETERSON, DA ;
SUHR, ST ;
RAY, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (25) :11879-11883
[6]  
HAJDUK SL, 1976, SCIENCE, V191, P858, DOI 10.1126/science.1251198
[7]   Optimal temporal delivery of bone marrow mesenchymal stem cells in rats with myocardial infarction [J].
Hu, Xinyang ;
Wang, Jianan ;
Chen, Jie ;
Luo, Ronghua ;
He, Aina ;
Xie, Xiaojie ;
Li, Jiahui .
EUROPEAN JOURNAL OF CARDIO-THORACIC SURGERY, 2007, 31 (03) :438-443
[8]   Bone marrow stem cells and liver disease [J].
Kallis, Y. N. ;
Alison, M. R. ;
Forbes, S. J. .
GUT, 2007, 56 (05) :716-724
[9]   USE OF A SEQUENCE-SPECIFIC DNA-BINDING LIGAND TO PROBE ENVIRONMENTS OF ECORI RESTRICTION ENDONUCLEASE CLEAVAGE SITES [J].
KANIA, J ;
FANNING, TG .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1976, 67 (02) :367-371
[10]  
Kicic A, 2003, J NEUROSCI, V23, P7742