Induction of accumulation and degradation of the 18.4-kDa oleosin in a triacylglycerol-storing cell culture of anise (Pimpinella anisum L.)

Planta ◽  
1994 ◽  
Vol 194 (1) ◽  
Author(s):  
Rudolf Radetzky ◽  
Ulrike Langheinrich
Keyword(s):  
Cell Culture ◽  
Pimpinella Anisum

Endogenous cytokinins during embryogenesis in an anise cell culture (Pimpinella anisum L.)

Planta ◽  
1984 ◽  
Vol 161 (3) ◽  
pp. 240-245 ◽  
Author(s):  
D. Ernst ◽  
D. Oesterhelt ◽  
W. Sch�fer
Keyword(s):  
Cell Culture ◽  
Pimpinella Anisum ◽  
Endogenous Cytokinins

Vergleichende Untersuchungen zur Bildung und Akkumulation von ätherischem Öl in der intakten Pflanze und in Zellkulturen von Pimpinella anisum L. / Comparative Studies on the Production and Accumulation of Essential Oil in the W hole Plant and in the Cell Culture of Pimpinella anisum L

1985 ◽  
Vol 40 (7-8) ◽  
pp. 465-468 ◽  
Author(s):  
J. Reichling ◽  
H. Becker ◽  
R. Martin ◽  
G. Burkhardt
Keyword(s):  
Cell Culture ◽  
Essential Oil ◽  
Callus Culture ◽  
Cell Cultures ◽  
Comparative Studies ◽  
Pimpinella Anisum ◽  
Whole Plant ◽  
Methyl Butyrate ◽  
First Time ◽  
Vergleichende Untersuchungen

Abstract Comparative studies on the essential oil of the whole plant and callus-and suspension cultures of Pimpinella anisum L. were carried out. Both the whole organism and the cell cultures were shown for the first time to be similar in their constituents e.g. anethole, pseudoisoeugenol-(2-methyl-butyrate), epoxy-pseudoisoeugenol-(2-methyl-butyrate) and β-bisabolene. In difference to the plant, the callus-culture contained myristicine.

A T.E.M. study of mouse mammary epithelial cell secretory differentiation cultured on collagen and Matrigel

1991 ◽  
Vol 49 ◽  
pp. 188-189
Author(s):  
W.N. Bentham ◽  
V. Rocha
Keyword(s):  
Cell Culture ◽  
Mammary Epithelial ◽  
Secretory Process ◽  
Cell Culture System ◽  
Protein Maturation ◽  
Cell Culture Techniques ◽  
Culture Techniques ◽  
Mouse Mammary Epithelial Cell ◽  
Secretory Differentiation

It has been an interest of our lab to develop a mammary epethelial cell culture system that faithfully duplicates the in vivo condition of the lactating gland. Since the introduction of collagen as a matrix on which cells are cultivated other E.C.M. type matrices have been made available and are used in many cell culture techniques. We have previously demonstrated that cells cultured on collagen and Matrigel do not differentiate as they do in vivo. It seems that these cultures often produce cells that show a disruption in the secretory process. The appearance of large ribosomal studded vesicles, that specifically label with antibody to casein, suggest an interruption of both protein maturation and secretion at the E.R. to golgi transition. In this report we have examined cultures on collagen and Matrigel at relative high and low seeding densities and compared them to cells from the in vivo condition.

Solid-phase immunoelectron microscopy for rapid diagnosis of enteroviruses

1984 ◽  
Vol 42 ◽  
pp. 226-227 ◽  
Author(s):  
K. Pegg-Feige ◽  
F. W. Doane
Keyword(s):  
Electron Microscopy ◽  
Cell Culture ◽  
Immunoelectron Microscopy ◽  
Detection Method ◽  
Solid Phase ◽  
Protein A ◽  
Plant Viruses ◽  
Rapid Diagnosis ◽  
Virus Diagnosis ◽  
Antiviral Antibody

Immunoelectron microscopy (IEM) applied to rapid virus diagnosis offers a more sensitive detection method than direct electron microscopy (DEM), and can also be used to serotype viruses. One of several IEM techniques is that introduced by Derrick in 1972, in which antiviral antibody is attached to the support film of an EM specimen grid. Originally developed for plant viruses, it has recently been applied to several animal viruses, especially rotaviruses. We have investigated the use of this solid phase IEM technique (SPIEM) in detecting and identifying enteroviruses (in the form of crude cell culture isolates), and have compared it with a modified “SPIEM-SPA” method in which grids are coated with protein A from Staphylococcus aureus prior to exposure to antiserum.

Automated cell counting of astrocytes on patterned substrates containing aliphatic and charged properties

1995 ◽  
Vol 53 ◽  
pp. 974-975
Author(s):  
W. Shain ◽  
H. Ancin ◽  
H.C. Craighead ◽  
M. Isaacson ◽  
L. Kam ◽  
...  
Keyword(s):  
Cell Culture ◽  
Cell Attachment ◽  
Culture Method ◽  
Cell Counting ◽  
Data Sets ◽  
Nuclear Staining ◽  
Double Positive ◽  
A Cell ◽  
Wafer Test ◽  
Cell Densities

Neural protheses have potential to restore nervous system functions lost by trauma or disease. Nanofabrication extends this approach to implants for stimulating and recording from single or small groups of neurons in the spinal cord and brain; however, tissue compatibility is a major limitation to their practical application. We are using a cell culture method for quantitatively measuring cell attachment to surfaces designed for nanofabricated neural prostheses.Silicon wafer test surfaces composed of 50-μm bars separated by aliphatic regions were fabricated using methods similar to a procedure described by Kleinfeld et al. Test surfaces contained either a single or double positive charge/residue. Cyanine dyes (diIC18(3)) stained the background and cell membranes (Fig 1); however, identification of individual cells at higher densities was difficult (Fig 2). Nuclear staining with acriflavine allowed discrimination of individual cells and permitted automated counting of nuclei using 3-D data sets from the confocal microscope (Fig 3). For cell attachment assays, LRM5 5 astroglial cells and astrocytes in primary cell culture were plated at increasing cell densities on test substrates, incubated for 24 hr, fixed, stained, mounted on coverslips, and imaged with a 10x objective.

Sign in / Sign up

Export Citation Format

Share Document