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J Forejt

Publications and source records attributed to J Forejt.

At least 55 records · Page 3Linked to original sources

Neuropsychiatric aspects of AIDS: a case report.

The acquired immune deficiency syndrome (AIDS) is a diverse disease that can affect all the systems of the human body. Frequently it can present initially as a neurologic or psychiatric illness due in part to the various infectious and neoplastic illnesses often encountered in susceptible individuals. Psychiatrists should be aware of the signs and symptoms of AIDS since they can be in the position to make the diagnosis first. A case of AIDS presenting as a psychiatric illness is described and its implications discussed further.

Acquired Immunodeficiency Syndrome↗

Supertypic HLA-Bw4 antigen detected by a new monoclonal antibody.

A monoclonal antibody, HLAO1, was prepared by immunizing BALB/c mice with human lymphocytes of known HLA genotype. The monoclonal antibody is cytotoxic, of the IgG 2b isotype and binds to a protein of Mr 43,000 noncovalently associated with the beta 2-microglobulin. Genetic analysis proved complete concordance in the expression of the antigenic determinant defined by this monoclonal antibody and the presence of a supertypic (public) antigen, the HLA-Bw4. As expected, the monoclonal antibody also reacted with the antigens of HLA-A locus, A23, A24, and A32. The computer analysis of HLAO1 antibody binding to the Bw4/Bw6 heterozygous lymphocytes gave the approximate number of antigenic determinants, n = 2.2 X 10(4)/cell, and Ka = (5.9 +/- 0.8) X 10(9) M-1. Besides its potential immunochemical applications, the HLAO1 monoclonal antibody can become a useful tool in routine cytotoxicity typing of HLA antigens on peripheral lymphocytes.

Animals↗

Recessive lethal t haplotypes increase the frequency of the partial trisomy of chromosome 17 (including the T-t complex) among offspring of T(16;17)43H female mice.

The male-sterile reciprocal autosomal translocation T(16;17)43H displays a high frequency of adjacent-2 disjunction in meiosis of translocation heterozygotes. One haploid product of this abnormal chromosome segregation leads to viable partial trisomy of chromosome 17 after fertilization. The frequency of trisomics increases in the progeny of T43H/+ females when the wild-type allelic form of T-t complex is substituted for t12, tw32 or t6 recessive lethal haplotypes. Indirect evidence supports the idea that the suppression of crossing-over by t haplotypes is linked with the increase in adjacent-2 disjunction and subsequent Ts43H trisomy. The possible use of Ts43H trisomy for genetic dissection of the T-t complex is briefly discussed.

Animals↗

Chromosomal and genic sterility of hybrid type in mice and men.

Three mouse models of male-limited, hybrid-type sterility are available: the sterility controlled by the T-t genetic complex, the hybrid sterility system including the Hst-1 gene, and the sterility of carriers of various chromosomal anomalies. A large body of experimental evidence has been gathered on the nonrandom attraction between X chromosome and rearranged autosomes in meiosis of carriers of various male-sterile chromosomal rearrangements in mice and men. A hypothesis is evaluated relating the X-autosomal interaction to spermatogenic breakdown. New data on the structure of t haplotypes indicate the presence of chromosomal inversions, and this might point to a chromosomal type of sterility of tx/ty hybrids. Gene hybrid sterility-1 is responsible for different fertility of male hybrids between certain laboratory and wild mice. The availability of wild mice (Mus musculus) derived inbred strains PWB, PWD, and PWK may facilitate further study of the hybrid sterility phenomenon in the mouse.

Animals↗

Establishment and characterization of the pluripotent mouse teratocarcinoma cell line TCE.

Embryonal carcinoma cells, the stem cells of teratocarcinomas, are a convenient model system for the study of embryonic development and cell differentiation. We established the pluripotent teratocarcinoma cell line TCE from embryoid bodies of teratocarcinoma strain OTT6050. The feeder independent cell line was characterized with regard to karyotype, differentiation capacities, developmentally regulated gene products, such as alkaline and acid phosphatase, cell surface markers, and by intermediate filament proteins. These parameters are discussed with respect to the developmental potency of the cell line TCE.

Acid Phosphatase↗

Establishment of a pluripotent embryonal carcinoma cell line not expressing SSEA-1 and ECMA-7 phenotypes.

A murine embryonal carcinoma (EC) cell line heterozygous for t0 recessive lethal mutation has been established from an embryo-derived transplantable teratocarcinoma TC1Ph of the genotype (129-T/t0 X C3H/Di)t0/+. The EC cell line, designated EC1Ph, and two cloned sublines, EC1Ph/a and EC1Ph/b, maintain the diploid karyotype (40, XY) and give rise to teratocarcinomas with differentiated derivatives of EC cells after inoculation into syngeneic recipients. The cloned sublines express low or zero amounts of SSEA-1 and ECMA-7 stage-specific antigens. At some passages, the EC1Ph line and the cloned subline EC1Ph/b express a significant quantity of class I H-2 antigens. This unusual EC phenotype resembles that of human teratocarcinoma cell lines.

Animals↗

Gene expression of differentiated parent in teratocarcinoma cell hybrids. Repression or reprogramming?

The hybrid cell line H422 was constructed by fusing embryonal carcinoma (EC) cells of the PCC4AzaRCapR cell line with lymphocytes from a 129-tw32 mouse inbred strain female. An apparently complete extinction of stage-specific gene products of the lymphocyte parent was inferred from comparison of protein maps in two-dimensional PAGE of parental and hybrid cells, and from the reactivity patterns of monoclonal antibodies in radioimmunobinding assays. Furthermore, the hybrid cells display a true EC phenotype and EC functions, tumorigenicity and pluripotency. Taken together, the available evidence suggests either that the lymphocyte genome is a 'silent passenger' as far as the differentiated functions of hybrid cells are concerned, or that the developmentally restricted lymphocyte genome is reprogrammed in the hybrid cells back to a non-determined stage and both genomes thus act in a concerted manner.

Animals↗

A gene controlling teratocarcinoma graft rejection mapped inside the t0 haplotype.

The embryo-derived teratocarcinoma TC1Ph of the genotype (129 t0/T X C3H)t0/+ and embryonal carcinoma (EC) cell line EC1Ph, established from the TC1Ph, were used as grafts for mice differing only at the T-H-2 interval of chromosome 17. Using exceptional recombinants in this chromosome region a two-gene model of genetic control of EC histocompatibility was proposed. The Cech-1 gene situated at the T end of the T-H-2 interval would control expression of the EC histocompatibility gene located near the H-2 complex.

Animals↗

XY pair associates with the synaptonemal complex of autosomal male-sterile translocations in pachytene spermatocytes of the mouse (Mus musculus).

Analysis of the chromosome behaviour at pachytene has been performed by means of the silver staining technique visualizing the synaptonemal complexes (SCs) in male mice heterozygous for the male-sterile translocations T(5;12)31Hm T(16;17)43H and T(7;19)145H, respectively. the T(9;17)138Ca male heterozygotes and T43H/T43H homozygous males were used as fertile controls. The sterile mice displayed a high frequency (about 60%) of pachytene spermatocytes with autosomal translocation configuration located in close vicinity of the XY pair. The dense round body (XAB), normally located near the X-chromosome axis in fertile males, exhibited abnormal affinity to translocation configuration in the sterile translocation heterozygotes. The incomplete synapsis of autosomes involved in translocation configuration was observed in more than 70% of the pachytene spermatocytes with the male-sterile translocations but less than 20% of the cells from T138Ca fertile male.s. A hypothesis relating the spermatogenic arrest of carriers of male-sterile rearrangements to the presumed interference with X chromosome inactivation in male meiosis is discussed.

Animals↗

[Fertility and the cytogenetic analysis of the early embryogenesis stages in mice with T(16, 17)43H chromosomal translocation].

Male mice heterozygous for double translocations, involving chromosome 17, T(16, 17)43H (reciprocal) and Rb (16, 17)7 Bnr (Robertsonian), as well as mice with partial trisomy for centromeric region of chromosome 17(Ts17(16)T43H) are fertile but demonstrate a high rate of sterile matings. On the 3rd day of gestation in the progeny of males heterozygous for double translocations chromosomal aberrations were shown in 9,5% of all cleaving embryos. The number of blastomeres in embryos with partial trisomy or monosomy of chromosome 17 or 16 corresponds well to that in embryos with normal karyotype. Partial trisomy Ts17(16)T43H does not affect cleavage and early postimplantation development but may cause growth retardation during major organogenesis. Some of these embryos are probably eliminated by the end of gestation or soon after birth. Mice with translocation T43H are useful tools for studying the action of different parts of chromosome 17 at different stages of ontogenesis.

Animals↗

Partial trisomy (including T-t gene complex) of the chromosome 17 of the mouse. The effect on male fertility and the transmission to progeny.

The animals with partial trisomy of chromosome 17, Ts(17A1-17B) 43H, were recovered among progeny of females heterozygous for T(16;17)43H "male-sterile" translocation. The trisomics as well as Rb7Bnr/T43H hybrids of both sexes were fertile, although the male fertility was significantly reduced in comparison with T43H/T43H homozygotes and males without chromosomal rearrangements. Ts43H trisomy acts as a semilethal aneuploidy since a significant deficiency of Ts43H animals was observed in progeny of Ts43H parent, while the expected proportion of trisomic embryos was found up to the 18th day of embryonic development.

Animals↗

Synaptonemal complexes of mouse and human pachytene chromosomes visualized by silver staining in air-dried preparations.

A new method is described which allows light microscopy visualization of the synaptonemal complexes in primary spermatocytes. The conventional acetic acid-alcohol fixed and air-dried preparations can be used for the modified silver staining technique. Several hundred pachytene spermatocytes from a single mouse testis or human testicular biopsy can be examined. The prospective utilization of the present method is briefly discussed.

Animals↗

Meiotic studies of translocations causing male sterility in the mouse. II. Double heterozygotes for Robertsonian translocations.

Unusual meiotic behavior of the XY chromosome pair was observed in sterile male mice doubly heterozygous for two Robertsonian translocations, Rb(16.17)7Bnr and Rb(8.17)1Iem. Nonrandom association between the X chromosome and the translocation configuration, ascertained from the frequencies of relevant C-band contacts, was found in 9 of 10 sterile males. Besides the nonrandom association, the XY chromosomes showed signs of impaired condensation, as judged by measurement of their lengths at diakinesis/MI of the first meiotic division. In contrast, neither nonrandom contact nor decondensation of the XY chromosomes pair was found in fertile males heterozygous for a single Robertsonian translocation, Rb1Iem or Rb7Bnr. The present observations lend indirect support to the working hypothesis advanced previously, the assumption that interference with X-chromosome inactivation is a possible cause of spermatogenic breakdown in carriers of various male-sterile chromosomal transloations. Alternative explanations of the available data, which cannot be ruled out, are briefly discussed.

Animals↗

Meiotic studies of translocations causing male sterility in the mouse. I. Autosomal reciprocal translocations.

A new meiotic phenomenon is described in male heterozygous for the male-sterile translocations T(10;13)199H, T(16;17)43H, and T(7;19)145H. The phenomenon consists of a nonrandom contact between the C bands of the X chromosome and the translocation configuration in diakinesis/metaphase I plates. Translocation configurations with positively heteropycnotic regions, oftern associated with the allocyclic X chromosome, are found in some early diakineses that have not been overtreated with alkali. Such heteropycnosis of a part of translocated autosome, apparently in phase with the allocyclic X, is typical for all three male-sterile translocations. In contrast to these findings, neither nonrandom contacts nor positive heteropycnosis of the translocation configuration can be found in males heterozygous for the translocation T(9;17)138Ca, which does not impair spermatogenesis. Dissociation of the X and Y at diakinesis is significantly enhanced in sterile males, though the occurrence of dissociation is evidently not related to the presence of the C-band contact between translocated chromosomes and the X. A working hypothesis is proposed, relating the observed nonrandom C-band contact and heteropycnosis of translocated chromosomes to a presumed impairment of X inactivation in primary spermatocytes and to consequent failure of spermatogenesis. An alternative explanation cannot be excluded, however, which would account for the hitherto available data wihtout postulating any causal relationship between the meiotic findings and male sterility. Both alternatives are amenable to experimental verification.

Animals↗