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Biomedical subjects

M H Johnson

Publications and source records attributed to M H Johnson.

At least 289 records · Page 16Linked to original sources

The developmental potential of mouse 16-cell blastomeres.

Based on the criteria of relative size and cell surface polarization, subpopulations of outer (larger, polar) and inner (smaller, apolar) blastomeres have been isolated from mouse 16-cell morulae and reaggregated in groups of 16 cells, and the developmental potential of the aggregates has been assessed both in vitro and in vivo. Aggregates of outer, inner, or mixed groups of cells all formed blastocysts which outgrew and contained both characteristic trophectoderm and alkaline phosphatase positive inner cell masses in vitro. However, significant differences were observed in the timing of blastocyst formation, depending on cell type. Aggregates of outer cells recompacted more slowly, commenced fluid accumulation earlier, and contained more cells at the blastocyst stage than did inner cell aggregates. Aggregates containing both outer and inner cells were intermediate. Postimplantation development of blastocysts derived from aggregates of outer or inner cells, after transfer to pseudopregnant recipients, was normal and comparable to zona-intact control embryos. This relationship between the expression of different morphological and behavioural properties by the precursor cells of the trophectoderm and inner cell mass and the existence of totipotent cells in both outer and inner subpopulations is discussed.

Animals↗

Nitrocellulose immunofixation following agarose electrophoresis in the study of immunoglobulin G subgroups in unconcentrated cerebrospinal fluid.

A method is presented which enables the study of cerebrospinal fluid proteins in minimal volumes of unconcentrated fluid. The method involves agarose electrophoresis followed by transfer of the proteins to a nitrocellulose membrane and then demonstration of their distribution using a double-antibody immunoperoxidase technique. The method is used here for the study of immunoglobulin G and its subgroups, and clearly shows that the oligoclonal pattern observed in multiple sclerosis is not restricted to any one subgroup.

Collodion↗

Hemoglobin Queens: alpha 34 (B15) Leu-Arg structural and functional properties and its association with Hb E.

Hemoglobin Queens: alpha 34 (B15) Leu-Arg was found in association with Hb E in a Vietnamese boy. The observed microcytosis and hypochromia were due to Hb E, which also occurred in other members of this family. The functional properties of Hb Queens in the absence and presence of allosteric effectors were normal. The abnormal hemoglobins appear to be unrelated to the hyperbilirubinemia that was observed at birth.

Amino Acids↗

The transition from maternal to embryonic control in the 2-cell mouse embryo.

The development of the early 2-cell mouse embryo to the late 2-cell stage is marked by the appearance between 23 and 26 h post-insemination of a complex of polypeptides of mol. wt. approximately 67 K. Addition of alpha-amanitin between 18 and 21 h post-insemination prevents or reduces the subsequent appearance of these polypeptides. Addition of alpha-amanitin after 21 h does not obviously affect the appearance of the approximately 67 K polypeptides. A major change in synthetic profile occurs between 29 and 32 h post-insemination involving many polypeptides. Addition of alpha-amanitin to 2-cell embryos prior to 29 h post-insemination prevents the appearance of the new polypeptides observed during this major change but does not prevent the disappearance of the old polypeptides. In contrast, addition of alpha-amanitin after this time does not affect the appearance of the new polypeptides. This result, together with other evidence presented, suggests that during the 2-cell stage the embryonic genome shows transcriptional activity in two phases at 18-21 and 26-29 h post-insemination, that these transcripts are utilized soon after their synthesis, and that most maternal transcripts used before the second phase of embryonic transcription become ineffective soon afterwards.

Amanitins↗

Cross-tolerance between two brainstem sites supporting stimulation-produced analgesia.

Male albino Holtzman rats were stereotaxically implanted with two bipolar stimulating electrodes, aimed at the periaqueductal gray matter of the brainstem. Focal brain stimulation-produced analgesia was assessed by the tail-flick method. After establishing that focal brain stimulation elicited analgesia at both sites, behavioral tolerance (i.e., reduced analgesia) was induced at one site through repeated stimulation. Upon elicitation of tolerance at one site, stimulation was immediately switched to the other site (which had not been previously rendered tolerant) and analgesia was assessed. Tail-flick latencies revealed transfer of behavioral tolerance from the site given repeated stimulation to the site not given repeated stimulation. While the mechanism involved in this cross-tolerance is not known, a neurochemical substrate may be involved.

Animals↗

Intensity changes in the Doppler effect.

When a source moves in any direction, the source strength and the frequencies are altered by the Doppler effect. It is shown that the source strength divided by the cube of the frequency is a Lorentz invariant.

Journal Article↗

Measurement of body fluid proteins by polyacrylamide gel electrophoresis.

A development of the disc polyacrylamide gel electrophoretic system of Ornstein and Davis, which has been applied to the analysis of unconcentrated cerebrospinal fluid, is described. Modifications to the scanning densitometer have improved the signal:noise ratio of the gel scanning system. Using this technique, we have studied the dye-binding properties of albumin, and of beta- and gamma-globulins, and have shown that reproducible quantification of proteins can be achieved. The advantages of electrophoretic methods over immunochemical methods of quantification are discussed.

Cerebrospinal Fluid Proteins↗

Amino acid transport and exchange in preimplantation mouse embryos.

Between the 1-cell zygote and the early blastocyst stage of mouse embryos the net rate of uptake of methionine increased, the internal pool became progressively more expanded and less easily reached steady state, and the specificity of competitor amino acids changed. Sodium-dependent transport was first detected in compacted morulae (16--32-cell stage). Uptake of [14C]methylaminoisobutyric acid was detectable in blastocysts but not in unfertilized eggs. Efflux of methionine by an exchange transport system was detectable at all stages, but in intact blastocysts much higher external concentrations were required to activate exchange transport. An exchange system with properties similar to that operating at cleavage stages was exposed when blastocysts were collapsed with cytochalasin D. Since this exchange system was not detectable in isolated inner cell masses, it may be confined to the juxtacoelic surface of trophectoderm cells.

Amino Acids↗

Pimozide versus chlorpromazine in chronic schizophrenia: a 52 week double-blind study of maintenance therapy.

This study compared the effectiveness and safety of pimozide and chlorpromazine in the maintenance therapy of chronic schizophrenic outpatients. Forty-three patients were assigned in double-blind fashion to one of the drugs for the 52 week study. Both medication groups showed a general pattern of improvement over the course of the study, but there was no significant difference between the two groups. The results demonstrated the effectiveness and safety of pimozide in once daily administration. Previous research results showing the special utility of pimozide for the improvement of emotional withdrawal and social competence in schizophrenia were not replicated.

Adult↗

Compaction of the mouse embryo: an analysis of its components.

A variety of Agents (viz : cytochalasin D, colcemid, cytochalasin D+ colcemid, Ca2+-free medium, 7-ketocholesterol, cholesterol, concanavalin A, anti-embryonal carcinoma antiserum and tunicamycin) which modify the cell membrane and/or cytoskeleton were used to investigate the molecular and cellular basis of the intercellular and intracellular components of compaction and analyse the relationships between them. It was found that the individual components could be selectively dissociated from one another. Cell flattening and close intercellular apposition were the most sensitive features and affected by the majority of agents. Tight junctions did not form in the absence of intercellular apposition, however an apparently normal degree of intercellular apposition did not necessarily lead to the assembly of these junctions. Polarization of individual blastomeres, as assessed by the reorganization of the cell surface, was the component most resistant to experimental intervention since it occurred in the presence of all agents used, though it was modified by some of them. The result are discussed in terms of the molecular and cellular events underlying polarization, intercellular apposition and tight junction formation as well as the significance of these events for normal blastocyst formation.

Animals↗

Electrophoresis of CSF proteins.

In this review we have tried to indicate the potential importance and interest of the proteins of the CSF and have argued that only by electrophoresis can these be examined in context. Without the need for expensive or elaborate equipment, a small volume of CSF can be used to demonstrate the pattern of proteins present, various qualitative changes, and the amounts of some individual proteins. For routine work this is of practical help in the diagnosis of certain neurological conditions, and as a research tool it can be utilized to investigate changes in protein structure and function occurring as part of immune or other responses. Access to neural tissue is necessarily restricted, but there is a great deal to be learned from the CSF.

Blood-Brain Barrier↗