Differentiation of oxytalan fibres from elastic fibres with reagents for detection of magnesium

1992 ◽  
Vol 174 (4) ◽  
pp. 357-359 ◽  
Author(s):  
Wilhelm Müller ◽  
Raimund Firsching
2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Tu Vinh Luong ◽  
Sameh Abou-Beih ◽  
Jennifer Watkins ◽  
Emmanuel Tsochatzis ◽  
Massimo Pinzani ◽  
...  

AbstractThe literature on the contribution of elastic fibre deposition to alcohol-related liver disease (ARLD) is limited. We studied: (1) 180 liver biopsies from ARLD patients; (2) 20 ARLD explant livers; (3) 213 liver biopsies with non-ARLD injury. Elastic fibres were assessed in terms of their distribution around hepatocytes [pericellular elastosis (PCE)] and within bridging fibrous septa (septal elastosis) and scored using a semiquantitative system. We also investigated the composition of the elastic fibres (oxytalan, elaunin and mature elastic fibres) in 20 cases. PCE was associated with steatohepatitis in ARLD patients and with ARLD when compared to non-ARLD cases (p < 0.001). Oxytalan fibres were identified in PCE in ARLD biopsies and broken dense perisinusoidal mature elastic fibres in explanted livers. Septal elastosis increased from intermediate to advanced fibrosis stage. Early septal elastosis contained oxytalan fibres, whereas septal elastosis at more advanced stages contained mainly mature elastic fibres. PCE is a typical feature of steatohepatitis in ARLD and includes oxytalan fibres. Septal elastosis is a gradual process with a transition from oxytalan to mature elastic fibres usually present in explanted livers. There may be different dynamics in the assembly and reabsorption of pericellular and septal elastic fibres, and a potential role for stratification of patients with advanced stage ARLD.


1968 ◽  
Vol 42 (3-4) ◽  
pp. 309-330 ◽  
Author(s):  
B. R. Laurence ◽  
M. G. Simpson

(1) Staining methods using paraldehyde-fuchsin, chrome-haematoxylin, and alcian blue or astra blue following oxidation, have demonstrated the shape of the hook and other structures on the cephalic space of microfilariae. These structures are described for three species of the genus Brugia, B. malayi, B. pahangi and B. patei, and are compared with the related structures found in the genera Wuchereria, Loa, Cardiofilaria, Onchocerca, Mansonella, Dipetalonema and Litomosoides.(2) In Brugia the hook of the microfilaria is V-shaped and is supported basally by a pair of transverse basal pieces which are closely associated with an oral ring. Similar structures are found in the microfilariae of Wuchereria and Loa except that in Loa the hook is supported below by a semi-circular arch. In Brugia there is a row of three spines transversely on the cephalic space opposite the hook complex, the spines being markedly shorter in B. patei than in the other two species; in Wuchereria there is a single transverse row of four spines, and in Loa there are two or three transverse rows of spines, No spines arranged opposite the hook complex were observed in the other genera. The hook and associated structures in Cardiofilaria are similar in arrangement to those of Loa, and the small structures in Mansonella can possibly be derived from a similar arrangement. In Onchocerca the hook has the appearance of a broad plate and in Dipetalonema perstans part of the surface of the cephalic space appears to be involved with the small pointed “hook”. In Litomosoides the tip of the cephalic space is covered by a helmet-like structure carrying a pointed beak-like projection.(3) It is suggested, from their staining reactions, that the cephalic structures of microfilariae are particularly rich in disulphide bonds, suggesting the presence of cystine.(4) The staining methods also demonstrate an internal thread of tissue in microfilariae which extends in Brugia from the tip of the cephalic space back to the innen korper. A similar thread is present in the microfilaria of Wuchereria, Loa, Cardiofilaria and Mansonella but was not observed in the other genera, although a short thread of tissue was stained in the cephalic space in Onchocerca and Litomosoides. In Brugia, the buccal capsule, the pharynx and the pharyngo-intestinal valve develop around the pharyngeal thread of the microfilaria. The extreme end of the thread, around which the pharyngo-intestinal valve develops, differs in its staining reactions from the rest of the thread.(5) The staining reactions of the pharyngeal thread in the microfilaria of Brugia show resemblances to those of “elastic” fibres in other invertebrates and oxytalan fibres of vertebrates. The pharyngeal thread appears to contain an acid mucopolysaccharide component.(6) The possible functions of the cephalic and pharyngeal structures in the microfilariae are discussed briefly.(7) A staining routine for demonstrating the structures described in this paper is given in an appendix.


1987 ◽  
Vol 117 (1) ◽  
pp. 21-27 ◽  
Author(s):  
S.L. MERA ◽  
C.R. LOVELL ◽  
R.RUSSELL JONES ◽  
J.D. DAVIES

Thorax ◽  
1998 ◽  
Vol 53 (3) ◽  
pp. 193-196 ◽  
Author(s):  
B. Shteyngart ◽  
S. Chaiwiriyakul ◽  
J. Wong ◽  
J. O Cantor

1974 ◽  
Vol 49 (4) ◽  
pp. 207-209 ◽  
Author(s):  
R. W. Horobin ◽  
Linda Fleming ◽  
I. M. Kevill-Davies

2012 ◽  
Vol 443 (1) ◽  
pp. 297-305 ◽  
Author(s):  
Hiroaki Nakajima ◽  
Yoshiyuki Ezaki ◽  
Tomoyashu Nagai ◽  
Ryosuke Yoshioka ◽  
Genji Imokawa

We recently reported that overexpression of the elastase NEP (neutral endopeptidase) by fibroblasts plays a pivotal role in the mechanism of UVB-induced skin wrinkling by degrading dermal elastic fibres. Since UVB does not penetrate to the dermis, we hypothesized that factors secreted by UVB-exposed keratinocytes in the epidermis trigger fibroblasts in the dermis to increase their expression of NEP which then degrades the elastic fibres. In the present study, we characterized the epithelial–mesenchymal interaction between keratinocytes and fibroblasts which leads to increased expression of NEP. Human fibroblasts co-cultured with UVB-exposed human keratinocytes in cell inserts significantly increased their expression of NEP at the transcriptional, translational and enzymatic levels. Neutralizing antibodies to IL (interleukin)-1α or GM-CSF (granulocyte/macrophage colony-stimulating factor) significantly abolished the increased expression of NEP at the enzymatic levels in human fibroblasts co-cultured with UVB-exposed human keratinocytes, whereas neutralizing antibodies to IL-6, IL-8 or TNFα (tumour necrosis factor α) had no such effect. The addition of IL-1α or GM-CSF, but not TNFα, IL-6 or IL-8, at concentrations ranging from 1 to 10 nM, significantly stimulated the expression of NEP in human fibroblasts at the transcriptional and translational levels. These findings suggest that IL-1α and GM-CSF are intrinsic cytokines secreted by UVB-exposed keratinocytes that stimulate expression of NEP by fibroblasts.


Sign in / Sign up

Export Citation Format

Share Document