Development of bovine embryos on Vero/BRL cell monolayers (mixed co-culture)

2000 ◽  
Vol 54 (8) ◽  
pp. 1239-1247 ◽  
Author(s):  
A.M. Duszewska ◽  
Z. Reklewski ◽  
M. Pieńkowski ◽  
J. Karasiewicz ◽  
J.A. Modliński
1991 ◽  
Vol 35 (1) ◽  
pp. 216 ◽  
Author(s):  
H.S. Jiang ◽  
W.L. Wang ◽  
K.H. Lu ◽  
I. Gordon ◽  
C. Polge

1991 ◽  
Vol 35 (1) ◽  
pp. 187 ◽  
Author(s):  
C. Boccart ◽  
P. Mermillod ◽  
C. Delecoeuillerie ◽  
F. Dessy

1991 ◽  
Vol 35 (1) ◽  
pp. 295 ◽  
Author(s):  
Zhao Xiaoxia ◽  
Jin Zhanqun ◽  
Jiang Shie ◽  
Liu Jianmin ◽  
Zhu Yuding

1992 ◽  
Vol 70 (5) ◽  
pp. 1449-1453 ◽  
Author(s):  
K. Goto ◽  
N. Iwai ◽  
Y. Takuma ◽  
Y. Nakanishi

2001 ◽  
Vol 2001 ◽  
pp. 216-216
Author(s):  
N.M. Orsi ◽  
J.B. Reischl ◽  
H.J. Leese

In vitro-produced (IVP) bovine embryos are used in a wide range of biotechnologies but develop less well than their in vivo counterparts and can give rise to foetal/neonatal anomalies after embryo transfer. The quality of bovine IVP embryos and the systems in which they are produced are traditionally assessed in terms of morphological and developmental criteria; namely, embryo grade and blastocyst formation rate. Lane and Gardner (1996) showed that mouse embryos selected for transfer on the basis of a low glycolytic activity (conversion of glucose to lactate), measured non-invasively, were 4 times more likely to implant than those selected randomly. Comparable data are not available for bovine embryos. The aim of this study was to assess linear glycolytic index of cattle blastocysts in vitro as a marker of viability. We have measured glucose consumption and lactate production by individual bovine IVP embryos grown in cell-free conditions and in a novel co-culture system (Orsi et al., 2000) involving confluent bovine oviduct epithelial cell monolayers on permeable supports. This preparation allows the epithelial cells to be fed by a nutritionally-rich medium via the physiological, basal, route, while the apical medium, containing the embryos, is more dilute, mimicking oviduct fluid.


Author(s):  
K. Chien ◽  
I.P. Shintaku ◽  
A.F. Sassoon ◽  
R.L. Van de Velde ◽  
R. Heusser

Identification of cellular phenotype by cell surface antigens in conjunction with ultrastructural analysis of cellular morphology can be a useful tool in the study of biologic processes as well as in diagnostic histopathology. In this abstract, we describe a simple pre-embedding, protein A-gold staining method which is designed for cell suspensions combining the handling convenience of slide-mounted cell monolayers and the ability to evaluate specimen staining specificity prior to EM embedding.


Author(s):  
K. Chien ◽  
R. Van de Velde ◽  
I.P. Shintaku ◽  
A.F. Sassoon

Immunoelectron microscopy of neoplastic lymphoma cells is valuable for precise localization of surface antigens and identification of cell types. We have developed a new approach in which the immunohistochemical staining can be evaluated prior to embedding for EM and desired area subsequently selected for ultrathin sectioning.A freshly prepared lymphoma cell suspension is spun onto polylysine hydrobromide- coated glass slides by cytocentrifugation and immediately fixed without air drying in polylysine paraformaldehyde (PLP) fixative. After rinsing in PBS, slides are stained by a 3-step immunoperoxidase method. Cell monolayer is then fixed in buffered 3% glutaraldehyde prior to DAB reaction. After the DAB reaction step, wet monolayers can be examined under LM for presence of brown reaction product and selected monolayers then processed by routine methods for EM and embedded with the Chien Re-embedding Mold. After the polymerization, the epoxy blocks are easily separated from the glass slides by heatingon a 100°C hot plate for 20 seconds.


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