TY - JOUR
T1 - Trophic factors differentiate dopamine neurons vulnerable to Parkinson's disease
AU - Reyes, Stefanie
AU - Fu, Yuhong
AU - Double, Kay L.
AU - Cottam, Veronica
AU - Thompson, Lachlan H.
AU - Kirik, Deniz
AU - Paxinos, George
AU - Watson, Charles
AU - Cooper, Helen M.
AU - Halliday, Glenda M.
PY - 2013
Y1 - 2013
N2 - Recent studies suggest a variety of factors characterize substantia nigra neurons vulnerable to Parkinson's disease, including the transcription factors pituitary homeobox 3 (Pitx3) and orthodenticle homeobox 2 (Otx2) and the trophic factor receptor deleted in colorectal cancer (DCC), but there is limited information on their expression and localization in adult humans. Pitx3, Otx2, and DCC were immunohistochemically localized in the upper brainstem of adult humans and mice and protein expression assessed using relative intensity measures and online microarray data. Pitx3 was present and highly expressed in most dopamine neurons. Surprisingly, in our elderly subjects no Otx2 immunoreactivity was detected in dopamine neurons, although Otx2 gene expression was found in younger cases. Enhanced DCC gene expression occurred in the substantia nigra, and higher amounts of DCC protein characterized vulnerable ventral nigral dopamine neurons. Our data show that, at the age when Parkinson's disease typically occurs, there are no significant differences in the expression of transcription factors in brainstem dopamine neurons, but those most vulnerable to Parkinson's disease rely more on the trophic factor receptor DCC than other brainstem dopamine neurons. (C) 2013 Elsevier Inc. All rights reserved.
AB - Recent studies suggest a variety of factors characterize substantia nigra neurons vulnerable to Parkinson's disease, including the transcription factors pituitary homeobox 3 (Pitx3) and orthodenticle homeobox 2 (Otx2) and the trophic factor receptor deleted in colorectal cancer (DCC), but there is limited information on their expression and localization in adult humans. Pitx3, Otx2, and DCC were immunohistochemically localized in the upper brainstem of adult humans and mice and protein expression assessed using relative intensity measures and online microarray data. Pitx3 was present and highly expressed in most dopamine neurons. Surprisingly, in our elderly subjects no Otx2 immunoreactivity was detected in dopamine neurons, although Otx2 gene expression was found in younger cases. Enhanced DCC gene expression occurred in the substantia nigra, and higher amounts of DCC protein characterized vulnerable ventral nigral dopamine neurons. Our data show that, at the age when Parkinson's disease typically occurs, there are no significant differences in the expression of transcription factors in brainstem dopamine neurons, but those most vulnerable to Parkinson's disease rely more on the trophic factor receptor DCC than other brainstem dopamine neurons. (C) 2013 Elsevier Inc. All rights reserved.
KW - Deleted in colorectal cancer
KW - Dopamine neurons
KW - Orthodenticle homeobox
KW - 2
KW - Pitx3
KW - Substantia nigra
U2 - 10.1016/j.neurobiolaging.2012.07.019
DO - 10.1016/j.neurobiolaging.2012.07.019
M3 - Article
C2 - 22926168
SN - 1558-1497
VL - 34
SP - 873
EP - 886
JO - Neurobiology of Aging
JF - Neurobiology of Aging
IS - 3
ER -