scholarly journals Denervation of skin in neuropathies: the sequence of axonal and Schwann cell changes in skin biopsies

Brain ◽  
2007 ◽  
Vol 130 (10) ◽  
pp. 2703-2714 ◽  
Author(s):  
G. J. Ebenezer ◽  
J. C. McArthur ◽  
D. Thomas ◽  
B. Murinson ◽  
P. Hauer ◽  
...  
2019 ◽  
Vol 85 (6) ◽  
pp. 887-898 ◽  
Author(s):  
John Svaren ◽  
John J. Moran ◽  
Xingyao Wu ◽  
Riccardo Zuccarino ◽  
Chelsea Bacon ◽  
...  

1983 ◽  
Vol 6 (3) ◽  
pp. 218-227 ◽  
Author(s):  
H. C. Powell ◽  
R. R. Myers
Keyword(s):  

2001 ◽  
Vol 92 (1-2) ◽  
pp. 128-137 ◽  
Author(s):  
Luke Eckersley ◽  
Annick D. Ansselin ◽  
David R. Tomlinson

1997 ◽  
Vol 93 (6) ◽  
pp. 611-618 ◽  
Author(s):  
A. P. Mizisin ◽  
Henry C. Powell
Keyword(s):  

Author(s):  
W. Jurecka ◽  
W. Gebhart ◽  
H. Lassmann

Diagnosis of metabolic storage disease can be established by the determination of enzymes or storage material in blood, urine, or several tissues or by clinical parameters. Identification of the accumulated storage products is possible by biochemical analysis of isolated material, by histochemical demonstration in sections, or by ultrastructural demonstration of typical inclusion bodies. In order to determine the significance of such inclusions in human skin biopsies several types of metabolic storage disease were investigated. The following results were obtained.In MPS type I (Pfaundler-Hurler-Syndrome), type II (Hunter-Syndrome), and type V (Ullrich-Scheie-Syndrome) mainly “empty” vacuoles were found in skin fibroblasts, in Schwann cells, keratinocytes and macrophages (Dorfmann and Matalon 1972). In addition, prominent vacuolisation was found in eccrine sweat glands. The storage material could be preserved in part by fixation with cetylpyridiniumchloride and was also present within fibroblasts grown in tissue culture.


Author(s):  
R.L. Martuza ◽  
T. Liszczak ◽  
A. Okun ◽  
T-Y Wang

Neurofibromatosis (NF) is an autosomal dominant genetic disorder with a prevalence of 1/3,000 births. The NF mutation causes multiple abnormalities of various cells of neural crest origin. Schwann cell tumors (neurofibromas, acoustic neuromas) are the most common feature of neurofibromatosis although meningiomas, gliomas, and other neoplasms may be seen. The schwann cell tumors commonly develop from the schwann cells associated with sensory or sympathetic nerves or their ganglia. Schwann cell tumors on ventral spinal roots or motor cranial nerves are much less common. Since the sensory neuron membrane is known to contain a mitogenic factor for schwann cells, we have postulated that neurofibromatosis may be due to an abnormal interaction between the nerve and the schwann cell and that this interaction may be hormonally modulated. To test this possibility a system has been developed in which an enriched schwannoma cell culture can be obtained and co-cultured with pure neurons.


Author(s):  
R. R. Warner

Keratinocytes undergo maturation during their transit through the viable layers of skin, and then abruptly transform into flattened, anuclear corneocytes that constitute the cellular component of the skin barrier, the stratum corneum (SC). The SC is generally considered to be homogeneous in its structure and barrier properties, and is often shown schematically as a featureless brick wall, the “bricks” being the corneocytes, the “mortar” being intercellular lipid. Previously we showed the outer SC was not homogeneous in its composition, but contained steep gradients of the physiological inorganic elements Na, K and Cl, likely originating from sweat salts. Here we show the innermost corneocytes in human skin are also heterogeneous in composition, undergoing systematic changes in intracellular element concentration during transit into the interior of the SC.Human skin biopsies were taken from the lower leg of individuals with both “good” and “dry” skin and plunge-frozen in a stirred, cooled isopentane/propane mixture.


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