Recovery of Proteolipid Protein in Mice Heterozygous for the Jimpy Gene

1989 ◽  
Vol 53 (1) ◽  
pp. 279-286 ◽  
Author(s):  
Joyce A. Benjamins ◽  
Diane M. Studzinski ◽  
Robert P. Skoff ◽  
Liljana Nedelkoska ◽  
Elizabeth A. Carrey ◽  
...  
Keyword(s):  
2021 ◽  
Vol 22 (6) ◽  
pp. 3233
Author(s):  
Christopher Kapitza ◽  
Rittika Chunder ◽  
Anja Scheller ◽  
Katherine S. Given ◽  
Wendy B. Macklin ◽  
...  

Multiple sclerosis (MS) has been considered to specifically affect the central nervous system (CNS) for a long time. As autonomic dysfunction including dysphagia can occur as accompanying phenomena in patients, the enteric nervous system has been attracting increasing attention over the past years. The aim of this study was to identify glial and myelin markers as potential target structures for autoimmune processes in the esophagus. RT-PCR analysis revealed glial fibrillary acidic protein (GFAP), proteolipid protein (PLP), and myelin basic protein (MBP) expression, but an absence of myelin oligodendrocyte glycoprotein (MOG) in the murine esophagus. Selected immunohistochemistry for GFAP, PLP, and MBP including transgenic mice with cell-type specific expression of PLP and GFAP supported these results by detection of (1) GFAP, PLP, and MBP in Schwann cells in skeletal muscle and esophagus; (2) GFAP, PLP, but no MBP in perisynaptic Schwann cells of skeletal and esophageal motor endplates; (3) GFAP and PLP, but no MBP in glial cells surrounding esophageal myenteric neurons; and (4) PLP, but no GFAP and MBP in enteric glial cells forming a network in the esophagus. Our results pave the way for further investigations regarding the involvement of esophageal glial cells in the pathogenesis of dysphagia in MS.


2003 ◽  
Vol 170 (2) ◽  
pp. 870-877 ◽  
Author(s):  
Jayagopala Reddy ◽  
Estelle Bettelli ◽  
Lindsay Nicholson ◽  
Hanspeter Waldner ◽  
Mei-Huei Jang ◽  
...  

2005 ◽  
Vol 82 (3) ◽  
pp. 346-356 ◽  
Author(s):  
Fanxue Meng ◽  
Olga Zolova ◽  
Natalia A. Kokorina ◽  
Anna Dobretsova ◽  
Patricia A. Wight

1992 ◽  
Vol 31 (2) ◽  
pp. 231-244 ◽  
Author(s):  
J. Kamholz ◽  
M. Sessa ◽  
S. Scherer ◽  
H. Vogelbacker ◽  
K. Mokuno ◽  
...  

1994 ◽  
Vol 54 (1-2) ◽  
pp. 179 ◽  
Author(s):  
Silva Markovic-Plese ◽  
Hikoaki Fukoara ◽  
Ahmad Al-Sabbagh ◽  
Alessandro Sette ◽  
Vijay K. Kuchroo ◽  
...  

Development ◽  
1998 ◽  
Vol 125 (18) ◽  
pp. 3709-3718 ◽  
Author(s):  
M. Knipper ◽  
C. Bandtlow ◽  
L. Gestwa ◽  
I. Kopschall ◽  
K. Rohbock ◽  
...  

All cranial nerves, as well as the VIIIth nerve which invades the cochlea, have a proximal end in which myelin is formed by Schwann cells and a distal end which is surrounded by oligodendrocytes. The question which arises in this context is whether peripheral and central parts of these nerves myelinate simultaneously or subsequently and whether the myelination of either of the parts occurs simultaneously at the onset of the cochlea function and under the control of neuronal activity. In the present paper, we examined the relative time course of the myelinogenesis of the distal part of the VIIIth nerve by analyzing the expression of peripheral protein P0, proteolipid protein and myelin basic protein. To our surprise, we observed that the expression of myelin markers in the peripheral and central part of the intradural part of the VIIIth nerve started simultaneously, from postnatal day 2 onwards, long before the onset of cochlea function. The expression rapidly achieved saturation levels on the approach to postnatal day 12, the day on which the cochlea function commenced. Because of its importance for the neuronal and morphological maturation of the cochlea during this time, an additional role of thyroid hormone in cochlear myelinogenesis was considered. Indeed, it transpires that this hormone ensures the rapid accomplishment of glial gene expression, not only in the central but also in the peripheral part of the cochlea. Furthermore, an analysis of the thyroid hormone receptors, TRaplha and TRbeta, indicates that TRbeta is necessary for myelinogenesis of the VIIIth nerve. Rapid thyroid hormone-dependent saturation of myelin marker gene expression in Schwann cells and oligodendrocytes of the VIIIth nerve may guarantee nerve conduction and synchronized impulse transmission at the onset of hearing. The thyroid hormone-dependent commencement of nerve conduction is discussed in connection with the patterning refinement of central auditory pathways and the acquisition of deafness.


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