Dehydrated human amnion/chorion membrane allografts for myelomeningocele and wound reconstruction

Author(s):  
Jonlin Chen ◽  
Christopher D. Lopez ◽  
Alisa O. Girard ◽  
Mya Abousy ◽  
Richard J. Redett ◽  
...  
Keyword(s):  
Author(s):  
Douglas R. Keene ◽  
Gregory P. Lunstrum ◽  
Patricia Rousselle ◽  
Robert E. Burgeson

A mouse monoclonal antibody produced from collagenase digests of human amnion was used by LM and TEM to study the distribution and ultrastructural features of an antigen present in epithelial tissues and in cultured human keratinocytes, and by immunoaffinity chromatography to partially purify the antigen from keratinocyte cell culture media.By immunofluorescence microscopy, the antigen displays a tissue distribution similar to type VII collagen; positive staining of the epithelial basement membrane is seen in skin, oral mucosa, trachea, esophagus, cornea, amnion and lung. Images from rotary shadowed preparations isolated by affinity chromatography demonstrate a population of rod-like molecules 107 nm in length, having pronounced globular domains at each end. Polyacrylamide gel electrophoresis suggests that the size of this molecule is approximately 440kDa, and that it is composed of three nonidentical chains disulfide bonded together.


Author(s):  
Douglas R. Keene ◽  
B. Kerry Maddox ◽  
Marie B. Spurgin ◽  
Lynn Y. Sakai ◽  
Robert W. Glanville

A mouse monoclonal antibody was used to identify beaded aggregates found in guanidine extracts of human amnion as assemblies of fibrillin molecules. These aggregates were also shown to be a major component of extracellular matrix microfibrils. We further demonstrated that the periodicity of these aggregates can be increased when subjected to mechanical stress.Human amnion was extracted with guanidine and the extracted material purified using ion exchange and molecular sieve chromatography. A high molecular weight fraction was precipitated by dialyzing against dilute acetic acid. Part of the precipitate was suspended in 0.2 M ammonium bicarbonate buffer and rotary shadowed. A second portion was resuspended in culture medium containing antibody which recognizes matrix microfibrils, diluted 1:5 in ammonium bicarbonate and reacted for 120 minutes at room temperature. Antibody labeled precipitate was washed by repeated pelleting and resuspension in buffer and then incubated in Janssen GAM 5 nm gold conjugate for 60 minutes at room temperature.


1985 ◽  
Vol 110 (1_Suppla) ◽  
pp. S53-S54
Author(s):  
ST. NIESERT ◽  
M. D. MITCHELL ◽  
M. L. CASEY ◽  
P. C. MACDONALD

2019 ◽  
Vol 82 (2) ◽  
Author(s):  
Yi Lu ◽  
Qiong Zhou ◽  
Jiang‐Wen Lu ◽  
Wang‐Sheng Wang ◽  
Kang Sun

1997 ◽  
Vol 36 (1-2) ◽  
pp. 111-121 ◽  
Author(s):  
S.S Edwin ◽  
M.D Mitchell ◽  
D.J Dudley
Keyword(s):  

2021 ◽  
Vol 11 (6) ◽  
Author(s):  
Jiang‐Wen Lu ◽  
Wang‐Sheng Wang ◽  
Qiong Zhou ◽  
Li‐Jun Ling ◽  
Hao Ying ◽  
...  
Keyword(s):  

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