Intracellular Chemical Imaging of the Developmental Phases of Human Neuromelanin Using Synchrotron X-ray Microspectroscopy

被引:91
作者
Bohic, Sylvain [1 ,5 ]
Murphy, Karen [2 ,3 ]
Paulus, Werner [4 ]
Cloetens, Peter [5 ]
Salome, Murielle [5 ]
Susini, Jean [5 ]
Double, Kay [2 ,3 ]
机构
[1] Univ Grenoble 1, Inst Neurosci Grenoble GIN, INSERM, UMR S 836,U836 Team 6, F-38042 Grenoble, France
[2] Prince Wales Med Res Inst, Randwick, NSW 2031, Australia
[3] Univ New S Wales, Randwick, NSW 2031, Australia
[4] Univ Hosp, Inst Neuropathol, D-48149 Munster, Germany
[5] European Synchrotron Radiat Facil, Xray Imaging Grp, ID Beamline 22, F-38043 Grenoble, France
基金
英国医学研究理事会;
关键词
D O I
10.1021/ac801817k
中图分类号
O65 [分析化学];
学科分类号
070302 [分析化学]; 081704 [应用化学];
摘要
The microchemical environment of neuromelanin (NM) in whole neurons from formalin fixed and paraffin embedded human substantial nigra sections were characterized using synchrotron chemical X-ray microscopy. Concentrations of NM-associated elements increased in the developing brain; the highest levels of most elements were found in the mature brain but the temporal pattern of the accumulation of different elements varied. High spatial resolution investigations, using a unique hard X-ray nanoprobe, revealed iron-rich microdomains colocalized with other elements within the pigment. These microdomains represent the first visualization of a structure regulating the metal-binding properties of NM and supporting a physiological role for NM in the regulation of functionally important elements in pigmented neurons. Our results demonstrate that the local chemical environment of iron in NM is similar to that found in ferritin and points to a possible role of iron in NM biosynthesis. Intracellular speciation of sulfur contained in NM revealed the presence of reduced sulfur compounds and various forms of oxidized sulfur compounds which have not previously been reported. Further, a significant increase in sulfonate in NM in the mature brain suggests that in vivo metabolism of the pigment via an as yet unidentified pathway occurs. The current data add to our understanding of the development and regulation of NM in the human brain.
引用
收藏
页码:9557 / 9566
页数:10
相关论文
共 52 条
[1]
Synchrotron hard x-ray microprobe:: Fluorescence imaging of single cells [J].
Bohic, S ;
Simionovici, A ;
Snigirev, A ;
Ortega, R ;
Devès, G ;
Heymann, D ;
Schroer, CG .
APPLIED PHYSICS LETTERS, 2001, 78 (22) :3544-3546
[2]
BRASS SD, 2006, TOP MAGN RESON IMAG, V1, P31
[3]
LOW SELENIUM DIET AFFECTS MONOAMINE TURNOVER DIFFERENTIALLY IN SUBSTANTIA-NIGRA AND STRIATUM [J].
CASTANO, A ;
CANO, J ;
MACHADO, A .
JOURNAL OF NEUROCHEMISTRY, 1993, 61 (04) :1302-1307
[4]
'Rejuvenation' protects neurons in mouse models of Parkinson's disease [J].
Chan, C. Savio ;
Guzman, Jaime N. ;
Ilijic, Ema ;
Mercer, Jeff N. ;
Rick, Caroline ;
Tkatch, Tatiana ;
Meredith, Gloria E. ;
Surmeier, D. James .
NATURE, 2007, 447 (7148) :1081-U5
[5]
Classification of nerve cells from substantia nigra of patients with Parkinson's disease and amyotrophic lateral sclerosis with the use of X-ray fluorescence microscopy and multivariate methods [J].
Chwiej, J ;
Fik-Mazgaj, K ;
Szczerbowska-Boruchowska, M ;
Lankosz, M ;
Ostachowicz, J ;
Adamek, D ;
Simionovici, A ;
Bohic, S .
ANALYTICAL CHEMISTRY, 2005, 77 (09) :2895-2900
[6]
GLUTATHIONE-PEROXIDASE, GLIAL-CELLS AND PARKINSONS-DISEASE [J].
DAMIER, P ;
HIRSCH, EC ;
ZHANG, P ;
AGID, Y ;
JAVOYAGID, F .
NEUROSCIENCE, 1993, 52 (01) :1-6
[7]
Dawson R, 2003, ADV EXP MED BIOL, V526, P537
[8]
INCREASED NIGRAL IRON CONTENT AND ALTERATIONS IN OTHER METAL-IONS OCCURRING IN BRAIN IN PARKINSONS-DISEASE [J].
DEXTER, DT ;
WELLS, FR ;
LEES, AJ ;
AGID, F ;
AGID, Y ;
JENNER, P ;
MARSDEN, CD .
JOURNAL OF NEUROCHEMISTRY, 1989, 52 (06) :1830-1836
[9]
The comparative biology of neuromelanin and lipofuscin in the human brain [J].
Double, K. L. ;
Dedov, V. N. ;
Fedorow, H. ;
Kettle, E. ;
Halliday, G. M. ;
Garner, B. ;
Brunk, U. T. .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2008, 65 (11) :1669-1682
[10]
Double KL, 2006, J NEURAL TRANSM-SUPP, P119