RESUMEN
Intercellular communication was examined with intracellular electrical techniques in primary and transplanted rat liver cancers. Normal liver cells communicate rather freely with each other through permeable junctional membranes. Cancer liver cells show no communication at all; their surface membrane is a strong barrier to diffusion all around the cell. Cancer cells induce alterations in membrane permeability in normal liver cells; communication among the latter is markedly reduced when cancer cells grow near them.
Asunto(s)
Permeabilidad de la Membrana Celular , Membrana Celular/fisiología , Neoplasias Hepáticas/fisiopatología , Hígado/fisiología , Animales , Transporte Biológico , Técnicas de Cultivo , Electrofisiología/instrumentación , Matemática , Potenciales de la Membrana , Neoplasias Experimentales , RatasRESUMEN
Intercellular communication was examined in normal and cancerous isolated thyroids with an intracellular electrical technique. The cells of normal thyroid (rat, mouse, hamster, man) communicate, within any given follicle, through permeable junctions. The cells of a wide variety of thyroid cancers (rat, hamster) do not communicate to any detectable degree and have resting membrane potentials lower than those of normal cells.
Asunto(s)
Potenciales de la Membrana , Neoplasias de la Tiroides , Animales , Cricetinae , Humanos , Ratones , RatasRESUMEN
Cells of Chironomus salivary glands and Malpighian tubules have junctions of the "septate" kind. This is the only kind of junction discerned which is large enough to effect the existing degree of intercellular communication. The electron microscopic observations of the "septate" junction conform to a honeycomb structure, with 80-A-thick electron-opaque walls and 90-A-wide transparent cores, connecting the cellular surface membranes. A projection pattern of light and dark bands (the "septa") with a 150-A periodicity results when the electron beam is directed normal to any set of honeycomb walls. Treatment of the salivary gland cells with media, which interrupt cellular communication (without noticeable alteration of cellular adhesion) by reducing junctional membrane permeability or perijunctional insulation, produces no alterations in the junctional structure discernible in electron micrographs of glutaraldehyde-fixed cell material.
Asunto(s)
Uniones Intercelulares/ultraestructura , Glándulas Salivales/citología , Glándulas Salivales/ultraestructura , Animales , Adhesión Celular , Comunicación Celular , Chironomidae , Fijadores/farmacología , Glutaral/farmacología , Microscopía Electrónica , Modelos BiológicosRESUMEN
Intercellular communication was examined in regenerating rat liver and urodele skin, two tissues of fast but normal growth. In both, cellular communication is in general as good as in their respective normal intact state. This stands in striking contrast to the lack of cellular communication in tissues with cancerous growth. Upon wounding of the urodele skin, the normally permeable junctional membranes of cells near the wound border seal themselves off, thereby insulating the interiors of the communicated cell systems from the exterior. When the cells of two opposing borders make mechanical contact in the course of wound closure, communication between them ensues within 30 min. Within this period all cell movement also ceases ("contact inhibition"). The possible implications of these findings in the control of tissue growth are discussed.
Asunto(s)
Regeneración Hepática/fisiología , Regeneración/fisiología , Fenómenos Fisiológicos de la Piel , Cicatrización de Heridas , Animales , División Celular , Membrana Celular/fisiología , Permeabilidad de la Membrana Celular , Técnicas de Cultivo , Electrofisiología/instrumentación , Ratas , UrodelosRESUMEN
The permeability of junctions between cells of the same type (homologous junctions) is greatly increased by retinoic acid (10(-9)-10(-8) M), a probable morphogen, and this responsiveness is shared by a variety of normal and transformed cell types (Mehta, P.P., J.S. Bertram, and W.R. Loewenstein. 1989. J. Cell Biol. 108:1053-1065). Here we report that the heterologous junctions between the normal and transformed cells respond in the opposite direction; their permeability is reduced by retinoic acid (greater than or equal to 10(-9) M) and its benzoic acid derivative tetrahydrotetramethylnaphthalenylpropenylbenzoic acid (greater than or equal to 10(-11) M). The opposite responses of the two classes of junction are shown to be concurrent; in cocultures of normal 10T1/2 cells and their methylcholanthrene-transformed counterparts, the permeability of the heterologous junctions, which is lower than that of the homologous junctions to start with, falls (within 20 h of retinoid application), at the same time that the permeability of the homologous junctions rises in both cell types. Such a counter-regulation requires a minimum of three degrees of cellular differentiation. A model is proposed in which the differentiations reside in a trio of junctional channel protein. The principle of the model may have wide applications in the regulation of intercellular communication at tissue boundaries, including embryonic ones.
Asunto(s)
Comunicación Celular/fisiología , Uniones Intercelulares/fisiología , Tretinoina , Animales , Benzoatos/farmacología , Comunicación Celular/efectos de los fármacos , Diferenciación Celular , División Celular , Línea Celular , Línea Celular Transformada , Permeabilidad de la Membrana Celular , Uniones Intercelulares/efectos de los fármacos , Ratones , Modelos Biológicos , Retinoides/farmacología , Factores de Crecimiento Transformadores/farmacologíaRESUMEN
Retinoic acid (a possible morphogen), its biological precursor retinol, and certain synthetic derivatives of retinol profoundly change junctional intercellular communication and growth (saturation density) in 10T 1/2 and 3T3 cells and in their transformed counterparts. The changes correlate: growth decreases as the steady-state junctional permeability rises, and growth increases as that permeability falls. Retinoic acid and retinol exert quite different steady-state actions on communication at noncytotoxic concentrations in the normal cells: retinoic acid inhibits communication at 10(-10)-10(-9) M and enhances at 10(-9)-10(-7) M, whereas retinol only enhances (10(-8)-10(-6) M). In v-mos-transformed cells the enhancement is altogether lacking. But regardless of the retinoid or cell type, all growth responses show essentially the same dependence on junctional permeability. This is the expected behavior if the cell-to-cell channels of gap junctions disseminate growth-regulating signals through cell populations.
Asunto(s)
Comunicación Celular/efectos de los fármacos , División Celular/efectos de los fármacos , Uniones Intercelulares/efectos de los fármacos , Retinoides/farmacología , Animales , Benzoatos/farmacología , Línea Celular , Línea Celular Transformada , Permeabilidad de la Membrana Celular/efectos de los fármacos , Diterpenos , Relación Dosis-Respuesta a Droga , Uniones Intercelulares/metabolismo , Ésteres de Retinilo , Tretinoina/farmacología , Vitamina A/análogos & derivados , Vitamina A/farmacologíaRESUMEN
We studied the development of NCAM and gap junctional communication, and their mutual relationship in chick neuroectoderm in vitro. Expression of NCAM, as detected by monoclonal and polyclonal antibodies, and development of junctional communication, as detected by extensive cell-to-cell transfer of 400-500-D fluorescent tracers, occurred in cultures from stage-2 embryos onward. Both expressions presumably required primary induction. The differentiating cells formed discrete fields of expression on the second to third day in culture, with the NCAM fields coinciding with the junctional communication fields delineated by the tracers. Other neural differentiations developed in the following order: tetanus toxin receptors, neurofilament protein, and neurite outgrowth. Chronic treatment with antibody Fab fragments against NCAM interfered with the development of communication, suggesting that NCAM-mediated adhesion promotes formation of cell-to-cell channels. Temperature-sensitive mutant Rous sarcoma virus blocked (reversibly) communication and the subsequent development of neurofilament protein and neurites, but expression of NCAM continued.
Asunto(s)
Antígenos de Superficie , Comunicación Celular , Ectodermo/citología , Uniones Intercelulares/fisiología , Neuronas/citología , Animales , Antígenos de Superficie/inmunología , Virus del Sarcoma Aviar/inmunología , Axones/fisiología , Unión Competitiva , Adhesión Celular , Moléculas de Adhesión Celular , Diferenciación Celular , Embrión de Pollo , Técnicas de Cultivo , Técnica del Anticuerpo Fluorescente , Colorantes Fluorescentes , Fragmentos Fab de Inmunoglobulinas/inmunología , Filamentos Intermedios/fisiología , Isoquinolinas , Organismos Libres de Patógenos EspecíficosRESUMEN
The distribution of Ca2+ in the cytoplasm following a local rise in Ca2+ concentration is visualized by means of aequorin luminescence and a television system with an image intensifier. Diffusion of Ca2+ through the cytosol is so constrained that a rise in cytoplasmic Ca2+ concentration produced by local Ca2+ entry through cell membrane or by local Ca2+ injection is confined to the immediate vicinity of these sites. The diffusion constraints are lifted by treatment with cyanide or ruthenium red. Thus, energized calcium sequestering, probably by mitochondria, is the dominant factor in the constraints. In cell regions where the sequestering machinery is sufficiently dense, different Ca2+ message functions inside a cell may be effectively segregated, permitting private-line intracellular communication.
Asunto(s)
Calcio/metabolismo , Citoplasma/metabolismo , Citosol/metabolismo , Aequorina , Animales , Transporte Biológico Activo/efectos de los fármacos , Cianuros/farmacología , Difusión , Dípteros , Retículo Endoplásmico/metabolismo , Metabolismo Energético/efectos de los fármacos , Mitocondrias/metabolismo , Rojo de Rutenio/farmacología , Glándulas Salivales/metabolismo , Glándulas Salivales/ultraestructuraRESUMEN
When the sensory fiber of a Pacinian corpuscle (in cat mesentery) is transected (at the inferior mesenteric nerve) transduction fails within 30 hours: the nerve ending produces no generator potentials in response to mechanical stimulation. Electrically elicited nerve impulse conduction continues for at least another 18 hours. A transducer mechanism develops on a regenerating nerve fiber when this fiber enters the denervated corpuscle. Such transducer development takes place on myelinated fibers from the inferior mesenteric nerve, which normally supplies corpuscles, as well as on myelinated hypogastric nerve fibers, which normally do not go to corpuscles, including fibers larger than the original corpuscle afferents.
Asunto(s)
Mecanorreceptores/fisiología , Regeneración Nerviosa , Neuronas/fisiología , Potenciales de Acción , Animales , Gatos , Mesenterio/inervación , Fibras Nerviosas Mielínicas/trasplante , Conducción Nerviosa , Neuronas/trasplante , Trasplante Autólogo , Vejiga Urinaria/inervaciónRESUMEN
Calcium ion participates in maintaining electrical connections between the nerve cells of Retzius (Hirudo medicinalis). The conductance across the junction between these cells decreases with decreasing concentration of free, extracellular Ca(++) At a certain level of Ca(++) withdrawal from the cell system, junctional conductance reaches a critical low point at which the cells become functionally disconnected: the nerve impulses which are normally discharged in synchrony by the cells become asynchronous. These effects of Ca(++) on junctional connection are irreversible, in contrast to those on nonjunctional surface membrane permeability.
Asunto(s)
Calcio , Conducción Nerviosa/fisiología , Neuronas/fisiología , Animales , Permeabilidad de la Membrana Celular , Ácido Edético/farmacología , Técnicas In Vitro , Iones , SanguijuelasRESUMEN
Calcium takes part in maintaining ion communication between salivary gland cells (Chironomus thummi). Its withdrawal from the cell systems results in virtual disconnection of ion communication, at Ca(++) concentrations which do not noticeably affect cell adhesion. The junctional membrane surfaces. which are normally quite freely permeable to ions, become as impermeable as the nonjunctional membrane surfaces; each cell seals itself off irreversibly as a unit. In maintaining ion communication Mg(++) substitutes for Ca(++)
Asunto(s)
Calcio , Epitelio/fisiología , Animales , Permeabilidad de la Membrana Celular , Quelantes/farmacología , Ácido Edético/farmacología , Técnicas In Vitro , Iones , Magnesio , ÁcarosRESUMEN
The permeability of the cell-to-cell membrane channels in salivary gland cell junction (Chironomus thummi) was probed with fluorescent-labeled amino acids and synthetic or natural peptides. Molecules up to 1200 daltons pass through the channels with velocities depending on molecular size. Molecules of 1900 daltons or greater do not pass. This passage failure seems to reflect the normal size limit for junctional channel permeation; the channels continue to be permeated by the molecules up to 1200 daltons when these are mixed with the nonpermeant molecules. From this size limit a channel diameter of 10 to 14 angstroms is estimated.
Asunto(s)
Membrana Celular/fisiología , Animales , Transporte Biológico/efectos de los fármacos , Calcio/farmacología , Dípteros , Colorantes Fluorescentes/metabolismo , Técnicas In Vitro , Cinética , Peso Molecular , Péptidos/metabolismo , Glándulas Salivales/fisiología , Glándulas Salivales/ultraestructura , Relación Estructura-ActividadRESUMEN
The channels in the junctions of various mammalian cell types--primary cultures and lines--were probed with a series of linear fluorescent amino acid and peptide molecules of different size and charge. Permeability is limited by probe size and electronegativity, these two factors apparently being related reciprocally. In respect to both factors, mammalian junctional channels are more restrictive than insect channels; hence the mammalian channels are narrower, more polar, or both. The channels of the various mammalian cell types differed slightly from each other; in some types the serum of the culture medium affected the channel permeability.
Asunto(s)
Permeabilidad de la Membrana Celular , Animales , Línea Celular , Membrana Celular/fisiología , Células Cultivadas , Cricetinae , Técnica del Anticuerpo Fluorescente , Riñón , Ratones , Ratones Endogámicos BALB C , Especificidad de la EspecieRESUMEN
Asymmetric membrane junctions were formed in culture by pairing two cell types which, in their respective homologous junctions, have cell-cell channels of different permselectivities. The channels in the asymmetric junction, presumably made of unequal channel precursors, displayed directional permselectivity; fluorescent labeled glutamic acid (700 daltons), but not smaller and less polar permeant molecules, traversed the junction more readily in one direction than in the other. The favored direction was the one where the permeant passed first through the cell membrane that would have the less restrictive channels in a homologous junction. This directional selectivity requires no electric field across the junction and is thus distinct from a rectifying junction. The physiological potential of such directional molecular sieving for partitioning communication between tissue cells of different function and developmental fate are discussed.
Asunto(s)
Comunicación Celular , Uniones Intercelulares/fisiología , Canales Iónicos/fisiología , Animales , Transporte Biológico , Línea Celular , Permeabilidad de la Membrana Celular , Colorantes Fluorescentes , Canales Iónicos/ultraestructura , Potenciales de la Membrana , RatonesRESUMEN
Overexpression of the cellular src gene in NIH 3T3 cells causes reduction of cell-to-cell transmission of molecules in the 400- to 700-dalton range. This down-regulation of gap junctional communication correlates with the activity of the gene product, the protein tyrosine kinase pp60c-src. The down-regulation was enhanced by point mutation of Tyr527 (a site that is phosphorylated in pp60c-src and that inhibits kinase activity) or by substitution of the viral-src for the cellular-src carboxyl-terminal coding region. Mutation of Tyr416 (a site phosphorylated upon Tyr527 mutation) suppresses both the down-regulation of communication by Tyr527 mutation and that by gene overexpression. The regulation of communication by src may be important in the control of embryonic development and cellular growth.
Asunto(s)
Comunicación Celular , Uniones Intercelulares , Proteínas Tirosina Quinasas/genética , Proteínas Proto-Oncogénicas/fisiología , Animales , Línea Celular , Permeabilidad de la Membrana Celular , Regulación de la Expresión Génica , Ratones , Mutación , Fosforilación , Plásmidos , Proteínas Proto-Oncogénicas/genética , Proteínas Proto-Oncogénicas pp60(c-src) , Relación Estructura-Actividad , Transcripción Genética , Transfección , Tirosina/metabolismoRESUMEN
The cell-to-cell channels in the junctions of an insect salivary gland and of insect and mammalian cells in culture were probed with fluorescent molecules-neutral linear oligosaccharides, neutral branched glycopeptides, and charged linear peptides. From the molecular dimensions of the largest permeants and smallest impermeants the permeation-limiting channel diameter was obtained: 16 to 20 angstroms for the mammalian cells and 20 to 30 angstroms for the insect cells.
Asunto(s)
Glicopéptidos/metabolismo , Uniones Intercelulares/ultraestructura , Oligosacáridos/metabolismo , Glándulas Salivales/ultraestructura , Animales , Línea Celular , Chironomidae , Colorantes Fluorescentes , Ratones , Ratones Endogámicos BALB C , Modelos Moleculares , Conformación Proteica , Especificidad de la EspecieRESUMEN
We examined the effect of polyomavirus middle T antigen on cell-to-cell communication in rat F cells transfected with an inducible middle T recombinant DNA or infected with a conditional mutant virus. Junctional permeability fell (reversibly) when middle T transcription was induced or when middle T was switched to the transformation+ form. The effect correlates with the rise of protein tyrosine kinase activity.
Asunto(s)
Antígenos Virales de Tumores/fisiología , Comunicación Celular , Uniones Intercelulares/fisiología , Poliomavirus/fisiología , Animales , Células Cultivadas , Mutación , Proteínas Tirosina Quinasas/fisiología , Proteínas Proto-Oncogénicas/fisiología , Proteínas Proto-Oncogénicas pp60(c-src) , Ratas , TemperaturaRESUMEN
We examined the actions of the cellular src (c-src) and adenovirus E1A genes on junctional cell-to-cell communication. Neither gene causes complete transformation of NIH3T3 cells on its own, but the two do so in conjunction with one another. This cooperation goes hand in hand with summation of the actions of the two genes on junctional communication: junctional permeability is reduced when the cells are transfected with either gene; it is reduced significantly more when they are transfected with both. This cooperative loss of communication approaches the noncooperative loss induced by the viral src gene (v-src), chimeric c-src/v-src, or Tyr527-mutant c-src--genes that cause transformation on their own. This provides a rationale for the hitherto unexplained complementation of the two oncogenes in carcinogenesis; it is the expected behavior if the loss of communication is causal in the decontrol of growth in transformation.
Asunto(s)
Comunicación Celular , Transformación Celular Neoplásica , Proteínas Oncogénicas Virales/genética , Oncogenes , Proteínas Proto-Oncogénicas/genética , Proteínas Precoces de Adenovirus , Animales , Permeabilidad de la Membrana Celular , Ratones , Proteínas Proto-Oncogénicas pp60(c-src) , Transfección , Factor de Necrosis Tumoral alfa/farmacologíaRESUMEN
The permeability of the membrane surfaces where cells are in contact (junctional membranes) in Chironomus salivary glands depends on Ca(++) and Mg(++). When the concentration of these ions at the junctional membranes is raised sufficiently, these normally highly permeable membranes seal off; their permeability falls one to three orders, as they approach the nonjunctional membranes in conductance. This permeability transformation is achieved in three ways: (a) by iontophoresis of Ca(++) into the cell; (b) by entry of Ca(++) and/or Mg(++) from the extracellular fluid into the cell through leaks in the cell surface membrane (e.g., injury); or (c) by entry of these ions through leaks arising, probably primarily in the perijunctional insulation, due to trypsin digestion, anisotonicity, alkalinity, or chelation. Ca(++) and Mg(++) appear to have three roles in the junctional coupling processes: (a) in the permeability of the junctional membranes; (b) in the permeability of the perijunctional insulation; and (c) a role long known- in the mechanical stability of the cell junction. The two latter roles may well be closely interdependent, but the first is clearly independent of the others.
Asunto(s)
Calcio/metabolismo , Permeabilidad de la Membrana Celular/efectos de los fármacos , Magnesio/metabolismo , Animales , Transporte Biológico , Membrana Celular/fisiología , Dípteros/anatomía & histología , Electrofisiología/instrumentación , Iontoforesis , Potenciales de la Membrana/efectos de los fármacos , Modelos Teóricos , Glándulas SalivalesRESUMEN
The ion permeability of the membrane junctions between Chironomus salivary gland cells is strongly depressed by treatments that are generally known to inhibit energy metabolism. These treatments include prolonged cooling at 6 degrees -8 degrees C, and exposure to dinitrophenol, cyanide, oligomycin, and N-ethylmaleimide. Intracellular injection of ATP appears to prevent depression of junctional permeability by dinitrophenol or to reverse it. Ouabain, azide, p-chloromercuriphenylsulfonic acid, reserpine, and acetazolamide fail to depress junctional permeability. Thus the ion permeability of the junctional membranes appears to depend on energy provided by oxidative phosphorylation. Possible energy-linked processes for maintaining junctional permeability are discussed, including processes involving transport of permeability-modifying species such as Ca(++).