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L J Rubinstein

Publications and source records attributed to L J Rubinstein.

148 records · Page 9Linked to original sources

Simultaneous expression of glial fibrillary acidic (GFA) protein and neuron-specific enolase (NSE) by the same reactive or neoplastic astrocytes.

In normal cells of the central nervous system (CNS), glial fibrillary acidic (GFA) protein is demonstrable by immunohistochemistry in fibrillated astrocytes, and neuron-specific enolase (NSE) in neurons and their processes. However, it has been shown that NSE may also be expressed in reactive astrocytes and in various neoplastic cells of non-neuronal origin, including those of astrocytomas and glioblastomas. In the present study, a double-labelling technique using immunoperoxidase (PAP) and immunofluorescence (FITC) was employed to determine whether GFA protein and NSE could be expressed simultaneously by the same cell. This was found to be the case in some, but not in all reactive astrocytes in the human brain. In glial tumours, many of the neoplastic cells in the glioblastomas and astrocytomas examined demonstrated either GFA protein or NSE, but usually not both. However, occasional neoplastic cells in those gliomas were found to show both proteins. Because of the relatively low sensitivity of the FITC technique, the percentage of cells expressing both proteins could not be determined, but it is clearly possible for a single reactive or neoplastic astrocyte to demonstrate both GFA protein and NSE.

Antigen-Antibody Reactions↗

Kinetics of the human medulloblastoma cell line, D283 Med, maintained in an organ culture system. Autoradiographic study after cumulative labelling in vitro: similarities to the kinetics of human medulloblastoma in situ.

Cells of the human D283 Med medulloblastoma cell line were collected by gravity sedimentation and maintained in vitro in an organ culture system. The explants grew as clusters of small cells with scanty cytoplasm; some cells were arranged in solid trabeculae, sometimes forming rows and columns, and occasionally rosettes. The kinetic parameters were estimated after 6 days in vitro by cumulative labelling of the cultures with tritiated thymidine in three different experiments. The length of G2 phase (TG2) was obtained from an analysis of the fractions of continuously labelled mitoses (FCLM), the length of S phase (TS) from the median values of grains over mitotic figures (grain index, GI), and the other parameters from mathematical models that related growth fraction (GF), TG2, total cell cycle time (TC) and labelling index (LI) as a function of time. Mean GF, TC, TG1, TS and TG2 were estimated respectively to be 0.35, 30 h, 13 h, 10 h, and 7 h. These estimates correspond to those reported for human medulloblastomas in situ and confirm previous in vitro experiments which suggest that the organ culture technique is a suitable system for the study of cell kinetics in human malignant gliomas and for an analysis of the in vitro effects of chemotherapeutic agents.

Autoradiography↗