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A mutant of Tetrahymena thermophila with a partial mirror-image duplication of cell surface pattern. I. Analysis of the phenotype.

Cells of a mutant clone, CU-127, of Tetrahymena thermophila (formerly T. pyriformis, syngen 1) manifest three anatomical abnormalities. First, the stable number of ciliary meridians is 21-25, above the usual number (17-21) in this species. Second, up to 30% of the cells have two oral apparatuses (OAs), one normal and the other abnormal. Third, more than one-half of the cells possess two distinct sets of contractile vacuole pores (CVPs). In some living cells two contractile vacuoles are seen. These abnormalities have persisted unchanged during more than 500 generations of vegetative propagation, and are similarly expressed in subclones. The normal and abnormal OAs are topographically segregated, with normal OAs developing along the "primary oral axis" and abnormal OAs developing along a "secondary oral axis" that is situated 170 degrees of the cell circumference to the cell's right of the primary oral axis. CVPs always appear within this 170 degree arc and never within the complementary 190 degrees arc to the left of the primary oral axis. A unique feature of the CU-127 clone is the commonly expressed mirror image reversal of the structural pattern of OAs that develop along the secondary oral axis. The primordia of such OAs initially appear (as usual) to the cell's left of a ciliary meridian, but as membranelles develop the frequently come to be oriented in a mirror image of the normal pattern, and an undulating membrane sometimes develops on the wrong (left) side of the oral primordium. When two sets of CVPs are formed, their average positions are roughly equidistant with respect to the two oral axes, with the two sets located 50-60 degrees to the right and left respectively of the primary and secondary oral axis. Such cells are thus bilaterally symmetrical about a plane defined by the central longitudinal axis and the halfway point between the two CVP sets (see Fig. 25). This plane bisects the cell into a normal and a "reversed" half-cell. However, only oral asymmetry and large-scale CVP positioning are subject to such reversal; all ciliary meridians remain of normal asymmetry and all CVPs are situated on the left side of CVP meridians. The fact that major aspects of large-scale cellular organization can be reversed while the "fine-positioning" associated with the ciliary meridians remains normal indicates that the two aspects of cell organization are distinct.

Animals↗

[The mirror stage ("Stade du Miroir" by J. Lacan) as a crucial stage of development for finding one's identity - normal, neurotic, psychotic development].

The socalled "Mirror Stage" ("Stade du Miroir" by J. Lacan) seems to be a normal stage of development between the sixth and the eighteenth month of age. In the centre of this study you find terms of developmental psychology and especially of psychoanalysis like: 'mother-child relationship', 'first relationship to objects', 'passage from primary to secondary narcism', 'ego-ideal' and 'ideal of the ego' and others. The Mirror Stage seems to be especially important for the formation of the identity: wether the child becomes 'normal', 'neurotic' or 'psychotic'. Here we also find terms, invented by Lacan like the 'Real', the 'Imaginary' and the 'Symbolic'.

Body Image↗

Observations on the "dependent stage" of the "mirror focus".

The present communication was part of a larger study in which penicillin induced epileptogenic activity in the hippocampus of the "cerveau isolé cat" was investigated. The discharge contralateral to the side of the PCN focus, i.e., the mirror focus, was dependent upon the integrity of the commissural pathways. Interhippocampal latencies of bisynchronous epileptogenic discharge varied between 0 and 50 msec (mean 20). Interestingly the discharges could occur absolutely simultaneously and even more surprising, the mirror focus discharge occasionally led that in the primary focus! An interpretation as to how this might occur is given.

Animals↗

Pre-T cell lineage of hand-mirror cells in acute lymphoblastic leukemia.

Acute lymphoblastic leukemia was observed in a 64-year-old male patient with 50-80% hand-mirror cells in the peripheral blood and in the bone marrow. Immunologic surface marker tests indicated that the cells were non-T non-B lymphocytes; however, the addition of thymosin (fraction V) to the bone marrow cells induced the capability of mounting a positive local xenogeneic graft-versus-host reaction (GVHR), demonstrating the pre-T-cell lineage of the hand-mirror cells in this patient.

Animals↗

Mirror hand anomaly: reconstruction of the thumb, wrist, forearm, and elbow.

Surgical procedures and the results of reconstruction of the mirror hand anomaly are presented. The thumb was reconstructed by pollicization of the radial third finger and multiple muscle transfer. The function of wrist, forearm, and elbow improved with arthroplasty of the affected joints. The results of the follow-up are satisfactory. We believe that surgical treatment of the mirror hand should be started in early life.

Arm↗

A teaching mirror for patient's observations during indirect ophthalmoscopy.

We developed a technique by which patients can observe the central fundus of their own contralateral eye during indirect ophthalmoscopy. This is achieved by adding an angulated mirror to the side of the presently available teaching mirror of the indirect ophthalmoscope. Self-indirect ophthalmoscopy is also feasible when the light source is kept stable.

Humans↗

Eye movements and choice times in mirror image pattern discrimination.

This paper studied mirror image and nonmirror image pattern discrimination by measuring adults' eye movements as they responded to spatially simple or spatially complex stimulus pairs. Two measures were derived from the eye movement data; the average position of the subject's gaze as a function of time (scanpath), and the distribution of eye positions sampled over the patterns (dwell distribution). The data show that spatial complexity has a qualitative influence on the processing of mirror and nonmirror patterns, that spatially complex pairs tend to be scanned from left-to-right, and that peripheral features are not usually directly fixated. The data also bear on theories of symmetry perception, and indicate that symmetry is not always perceived in a holistic fashion.

Choice Behavior↗

[Anton-Babinski syndrome with recognition of the left upper limb on visualization in a mirror [author's transl)].

A patient presenting with an Anton-Babinski syndrome accompanied by a delusional conviction recognised her left upper limb with the aid of her right hand, but immediately denied its existence when she viewed it directly. In contrast, when placed in front of a mirror, she recognised this upper limb perfectly, recognition disappearing again when direct vision was associated with vision in the mirror. The authors suggest the possibility of a resurgence in adult life of the duality of the visual body image, direct or reflected, such as is normally experienced in childhood and, more prolonged, in identical twins.

Agnosia↗

Presbyopic drivers' vision through a convex rear view mirror.

BACKGROUND: Monovision is a commonly used modality for the presbyope who wants to wear contact lenses. If the add for near vision is in the left eye, driving an automobile creates a circumstance whereby the lens wearer cannot obtain a clear image in that eye of distant objects seen in the driver's side outside rear view mirror. METHODS: We have discovered that a stick-on convex mirror eliminates this problem by neutralizing either some or all of the power of the add. RESULTS: The driver wearing an add in the left eye can then obtain a clear image in that eye of objects behind and to the side of the automobile.

Automobile Driving↗

[Transvenous pacemaker implantation for sick sinus syndrome with mirror-image dextrocardia].

A case of sick sinus syndrome with mirror-image dextrocardia which was associated with bilateral superior vena cava and an absent inferior vena cava with azygos continuation is reported. A 45-year-old woman was referred to our hospital with the chief complaints of dizziness and palpitation. The electrocardiogram showed a atrial fibrillation with a 4-second period of asystole. A permanent endocardial bipolar demand pacemaker was inserted through the left superior vena cava. Since anomaly of venous system is commonly associated with mirror-image dextrocardia, the angiogram is necessary prior to permanent pacemaker implantation.

Dextrocardia↗

Immune activation of guinea pig lymphocytes type "cerebriform" and type "hand mirror". An ultrastructural study.

The fine structure of lymphocytes type "cerebriform" and type "hand mirror" from guinea pigs was analyzed. The cells were isolated from three groups of animals, immunized with BCG, F. tularensis (LVS) or plague vaccine (EV-Brubaker), respectively, and stimulated in vitro with the corresponding antigen six weeks after the immunizations. Both, the "cerebriform" and "hand mirror" lymphocytes were present in the T-cell fractions but not in the B-cell ones. Upon stimulation, these types of cells reacted uniformly, independently of the antigen used. This was expressed in cell volume increase, inversion of the nucleo-cytoplasm index, proliferation of organelles, hypertrophy of the Golgi complex, dispersion of the nuclear chromatin and an increase of the number of cytoplasmic projections. According to ultrastructural characteristics the subpopulation of the "cerebriform" lymphocytes was non-uniform. It is possible that some of the cells express cytotoxic functions.

Animals↗

[Hand-mirror cells acute lymphoblastic leukemia (L3)].

To our knowledge, this report represents the first confirmed case in Japan of a 15-year-old boy with acute lymphoblastic leukemia (ALL).L3 with hand-mirror cells (HMC) in the bone marrow. HMC lymphoid leukemia is an unusual variant of ALL in which the bone marrow lymphoblasts manifest distinctive hand-mirror morphologic features. HMC lymphoblast is characterized by an asymmetric foot-like cytoplasmic process that extends from the portion of the cell, thus giving it the light-microscopic appearance responsible for its name. Besides ALL, HMC has been reported in acute myeloblastic leukemia (AML), blastic crisis of chronic myelogenous leukemia, non-Hodgkin's lymphoma, and infectious mononucleosis. HMC has been reported to be prevalent in ALL.L1 and L2 as compared with L3.

Adolescent↗

Head formation at the basal end and mirror-image pattern duplication in Hydra vulgaris.

Head and foot in Hydra are organizing centers and considered to be sources of long-range inhibitory morphogens that prevent head and foot formation elsewhere. In a previous study the apparent long-range head inhibition was shown to coincide with long-range foot promotion exerted by the head. Here it is shown that: (1) ring-shaped pieces of the body column taken from a near-foot position form feet - frequently circular - if inserted into the midgastric region; this ectopic foot formation is strongly dependent on assistance by the head. (2) Bisection causes a transient increase in positional value at the wounded basal end of the upper body column. This transient development in the head direction in turn promotes ectopic foot formation by transplants and thus has an effect as though the source of a foot-inhibiting morphogen were removed. The existence of long-range foot inhibition is open to question. (3) If a ring with low positional value is present in the midgastric region, the increase in positional value at the basal end is stable and results in mirror-image head formation instead of foot regeneration in up to 100% of cases. Even before the ring forms a foot it acts like a ligature and subdivides the body column into two developmental compartments. (4) The basal head in turn organizes a mirror-image duplication of the body pattern. In pattern regulation, Hydra follows rules of intercalation known from other organisms.

Animals↗

Right aortic arch with mirror-image branching and coarctation of the aorta.

We report a case of right aortic arch with mirror-image branching and coarctation of the aorta and left ductus arteriosus in a 6-year-old boy. He was referred to Chang Gung Children's Hospital with suspected left ventricular failure. Physical examination revealed hypertension and a pulse discrepancy between the upper and lower extremities. Echocardiography and magnetic resonance imaging revealed a right aortic arch, a long segmental aortic coarctation, and a patent ductus arteriosus. In addition, mirror-image branching of the brachiocephalic vessels was found. The coarctation was resected and the ductus arteriosus was ligated. The postoperative recovery was uneventful and the blood pressure returned to normal. He remained normotensive and had no symptoms of heart failure within the 2 years of follow-up.

Aorta, Thoracic↗

Unfavorable prognostic significance of hand mirror cells in childhood acute lymphoblastic leukemia. A report from the childrens Cancer Study Group.

The prognostic significance of hand mirror cells (HMCs) in childhood acute lymphoblastic leukemia was determined by quantifying the percentage of these cells in the diagnostic bone marrow aspirates of previously untreated children entered on the Childrens Cancer Study Group protocol 141. Of 664 examinable patients, 39 (5.9%) had greater than 10% HMCs, and only four (0.6%) had greater than 30% HMCs. Compared with the entire study population, a greater proportion of children with more than 10% HMCs were older than 10 years of age, had hemoglobin levels greater than 10 g/dL, and had undifferentiated lymphoblast morphology. The children with more than 10% HMCs had a higher rate of bone marrow relapse, poorer disease-free survival, and shorter survival than patients with less than 10% HMCs. By multivariate analysis, HMC morphology was an independent, unfavorable prognostic factor.

Age Factors↗

Severe limb deficiencies, vertebral hypersegmentation, and mirror polydactyly: two additional cases that expand the phenotype to a more generalized effect on blastogenesis.

We report on 2 unrelated fetuses with a multiple congenital anomaly pattern of severe limb deficiencies, vertebral/rib alterations, and mirror polydactyly similar to that described previously by us [Urioste et al., Hum Genet 97:214-217, 1996]. In addition, the two cases we present here have a more extense alteration of blastogenesis, expanding the phenotype of the cases previously reported. We have suggested [Urioste et al., Hum Genet 97:214-217, 1996] that this condition may be caused by a mutation in a developmental control gene that affects body-plan organization. The minimal estimate of the prevalence of this new entity in our population (the Spanish Collaborative Study of Congenital Malformations, ECEMC) is 3.0/ 1,000,000 live births.

Abnormalities, Multiple↗

Avian transitin expression mirrors glial cell fate restrictions during neural crest development.

During development, trunk neural crest cells give rise to three primary classes of derivatives: glial cells, melanocytes, and neurons. As part of an effort to learn how neural crest diversification is regulated, we have produced monoclonal antibodies (MAbs) that recognize antigens expressed by neural crest cells early in development. One of these, MAb 7B3 (7B3), was found to recognize an avian transitin-like protein by co-immunostaining with a series of transitin-specific monoclonal antibodies and by Western blot analysis. In neural crest cell cultures, we found that 7B3 initially recognizes the majority of neural crest cells as they emerge from the neural tube. Subsequently, 7B3-immunoreactivity (IR) is progressively restricted to a smaller subpopulation of cells. In fully differentiated trunk neural crest cell cultures, 7B3-IR is expressed only by cells that do not express neuronal markers and lack melanin granules. During development in vivo, 7B3-IR is evident in neural crest cells on the medial, but not the lateral migration pathway, suggesting that it is not expressed by melanocyte precursors. Later, the antigen is detected in non-neuronal, presumptive glial cells in dorsal root ganglia (DRG) and sympathetic ganglia, as well as along ventral roots. Cultures of E5 DRG confirm that 7B3-IR is restricted to non-neuronal cells of ganglia, many of which closely associate with neuronal processes. Therefore, of the three major classes of differentiated trunk neural crest derivatives, 7B3 exclusively recognizes glial cells, including both satellite glia and Schwann cells. Since the pattern of 7B3 expression in vitro mirrors the pattern of glial cell fate-restrictions in the trunk neural crest lineage, and is expressed by neural crest-derived glia in vivo, we conclude that 7B3 is an early pan-glial marker for neural crest-derived glial cells and their precursors.

Animals↗