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Topic:Cell Culture

Cell culture in horses involves the in vitro cultivation of equine cells under controlled conditions. This technique is employed to study various cellular processes, including growth, differentiation, and response to external stimuli, in an isolated environment. Equine cell cultures can be derived from various tissues, such as skin, muscle, or bone, and are used in a range of research applications, including genetic studies, drug testing, and disease modeling. These cultures provide a valuable platform for understanding cellular mechanisms and developing therapeutic strategies. This page compiles peer-reviewed research studies and scholarly articles that explore the methodologies, applications, and findings related to cell culture in equine research.
Electron microscopy of the ventricular lining associated with the hypothalamus and median eminence of prepubertal female horses.
Journal of reproduction and fertility. Supplement    January 1, 1982   Volume 32 577-581 
Melrose PA, Douglas RH.Scanning electron microscopy showed that cells in the infundibular recess of prepubertal female horses were devoid of cilia and sparsely covered with stubby microvilli and small blebs, whereas superior ventricular areas were covered with cilia. Ciliated ependymal cells in supraoptic-suprachiasmatic areas were associated with extensive blebbing, and folded tissue adjacent to the inferior borders of the mamillary body displayed distinct bands of cilia regularly interrupted by areas of sparsely ciliated cells which appeared to be undergoing ciliogenesis. Arcuate ependymal areas had well developed...
Collection and cultivation in vitro of equine mammary macrophages.
American journal of veterinary research    November 1, 1981   Volume 42, Issue 11 1956-1958 
Anderson LW, Banks KL.Equine macrophages were obtained from female Shetland ponies by injection of Escherichia coli lipopolysaccharide through the lactiferous ducts of the mammary gland. After 6 to 11 days, balanced salt solution was injected into the mammary gland to wash out accumulated cells. Harvested cells contained a mixture of macrophages, lymphocytes, and neutrophils, with the majority of the cells of mononuclear type. In culture, cells adherent after 24 hours were characterized as macrophages by morphologic features, nonspecific esterase staining, and by the presence of complement and immunoglobulin recept...
Effects of cytotoxic drugs on cultured equine cells in vitro.
Equine veterinary journal    October 1, 1981   Volume 13, Issue 4 251-253 doi: 10.1111/j.2042-3306.1981.tb03509.x
Doyle A, Owen LN.Sixteen cytotoxic drugs used in cancer chemotherapy in man were studied for cytopathic effect on equine fibrosarcoma, melanoma and normal equine lung cells in vitro. Three drugs, vincristine, melphalan and methotrexate, produced cytopathic effect
Isolation and identification of equine lymphocytes and monocytes.
American journal of veterinary research    September 1, 1981   Volume 42, Issue 9 1651-1654 
Banks KL, Greenlee A.Various cell populations of equine mononuclear leukocytes were identified and isolated. Mononuclear leukocytes were concentrated by isopyknic centrifugation, using a solution of Ficoll and Hypaque. Three additional techniques were explored to separate monocytes from lymphocytes, and 3 methods were used to separate lymphocyte types. Cytochemical techniques for the detection of nonspecific esterase readily distinguished equine monocytes from lymphocytes. Peripheral blood lymphocytes were separated into at least 2 populations. One population had surface traits identical to thymocytes [ie, they re...
Isolation of cellulolytic phycomycete fungi from the caecum of the horse.
Journal of general microbiology    April 1, 1981   Volume 123, Issue 2 287-296 doi: 10.1099/00221287-123-2-287
Orpin CG.Microscopic examination of horse caecum contents revealed vegetative growth of phycomycete fungi on particles of digesta, and uniflagellated cells similar to fungal zoospores in the liquid phase. Three morphologically distinct isolates of strictly anaerobic phycomycete fungi were obtained from the caecum contents and cultured in vitro. Two of the isolates were able to utilize a wide range of plant carbohydrates for growth, including alpha-cellulose, xylan and particulate starch, and extensively digested water-insoluble plant tissues.
Culture of horse oocytes in vitro.
Journal of reproduction and fertility    January 1, 1981   Volume 61, Issue 1 213-215 doi: 10.1530/jrf.0.0610213
Fulka J, Okolski A.Oocytes were removed from follicles 5-30 mm in diameter. The germinal vesicle was present in 69.6% (23/33) of the oocytes at the start of culture, but after 20-24 and 40 h 70.5% (12/17) and 68.2% (43/63) of the oocytes were in metaphase I and metaphase II with first polar body extruded, respectively.
Propagation of equine infectious anemia virus in horse cell cultures.
Virologie    January 1, 1981   Volume 32, Issue 1 23-27 
Grădinaru DA, Stirbu C, Păltineanu D, Mironescu D, Manolescu N.The Wyoming strain of equine infectious anemia virus was adapted to cell cultures by 7 passages in horse leukocytes and 14 passages in fetal equine dermal and kidney cells. The virus was made evident by electron microscopy and immunodiffusion tests with antigens prepared from culture fluids.
In vitro host range of equine infectious anemia virus.
Intervirology    January 1, 1981   Volume 16, Issue 4 225-232 doi: 10.1159/000149271
Benton CV, Brown BL, Harshman JS, Gilden RV.Equine infectious anemia virus (EIAV) was successfully inoculated onto cell cultures of canine and feline origin, resulting in chronic infections in these cultures. Infection of equine cell cultures, which were the previous sole in vitro source demonstrated for virus production, was also performed for comparative purposes. Determination of the nature of the virus produced in the heterologous as well as the equine cells was accomplished in several ways. SDS-PAGE of purified virus from the different cell lines indicated very similar protein composition. Immunological identity was observed in gel...
[3H]5-HT binding sites and 5-HT-sensitive adenylate cyclase in glial cell membrane fraction.
Brain research    October 6, 1980   Volume 198, Issue 2 361-374 doi: 10.1016/0006-8993(80)90750-7
Fillion G, Beaudoin D, Rousselle JC, Jacob J.Glial cell membrane fractions were prepared using glial cells preparations isolated from horse brain striatum. [3H]5-HT binding was measured by the filtration technique and the adenylate cyclase activity determined by measuring the cAMP production using a radioimmunoassay. Serotonin binds to glial membrane fractions with an affinity corresponding to a dissociation constant Kd = nM. The corresponding site is serotoninergic specific: [3H]5-HT binding is inhibited by 5-HT agonists (5 OH NM-DMT, 5-MeOHT, 5-MeOH-DMT, NN-DMT) or antagonists (cinanserine, cyproheptadine, methysergide, LSD) and not (o...
Horse erythrocyte gangliosides: preparation of the major hematoside NeuNG1-Lac-Cer.
Lipids    September 1, 1980   Volume 15, Issue 9 682-685 doi: 10.1007/BF02534019
Maget-Dana R, Michalski JC.A simple method for the isolation of hematoside NeuNG1-Lac-Cer from horse erythrocytes is described. An aliquot of the crude ganglioside fraction was labeled by tritiated sodium borohydride after mild periodate oxidation. The compounds obtained were used as radioactive tracers in column chromatography. Gangliosides were applied onto a silicic acid column and eluted stepwise by solvents of steadily increasing polarity. The major ganglioside, NeuNG1-Lac-Cer, was eluted in a high yield by the solvent mixture chloroform/methanol/water (60:35:8, v/v/v).
An assessment of filamentous carbon fibre for the treatment of tendon injury in the horse.
The Veterinary record    March 8, 1980   Volume 106, Issue 10 217-221 doi: 10.1136/vr.106.10.217
Goodship AE, Brown PN, Yeats JJ, Jenkins DH, Silver IA.The results of an assessment of carbon fibre for biological use are given, with particular reference to the clinical use of the material in the treatment of equine tendon injury. Biocompatability of the fibres is assessed using fibroblast cell cultures and replacement of normal tendon with carbon fibre prostheses in experimental animals. The rationale and technique for using this material in clinical cases of tendon injury in the racehorse are described. Results are given from 62 implant operations in a limited series of 40 horses.
The direct influence of stallion semen on progesterone production in cultured corpus luteum cells.
Zentralblatt fur Veterinarmedizin. Reihe A    January 1, 1980   Volume 27, Issue 9-10 788-795 doi: 10.1111/j.1439-0442.1980.tb02032.x
Gregoraszczuk E, Okólski A, Galas J.No abstract available
Ultrastructure of Haemophilus equigenitalis, causative agent of contagious equine metritis.
American journal of veterinary research    January 1, 1980   Volume 41, Issue 1 127-132 
Swaney LM, Breese SS.Haemophilus equigenitalis, a proposed new species of Haemophilus and the causative agent of contagious equine metritis, a venereal disease of the horse, had ultrastructural characteristics of gram-negative bacteria. The organism additionally had a small, threadlike capsule that was removed by heating in phosphate-buffered saline solution. Heating also detached the outer membrane from the cytoplasmic membrane. The capsule could only be demonstrated when bacterial were stained with ruthenium red during the preparation of ultrathin sections. The gross morphology of newly isolated organisms (rodli...
The origin of nuclear bodies: a study of the undifferentiated epithelial cells of the equine small intestine.
The American journal of anatomy    January 1, 1980   Volume 157, Issue 1 61-70 doi: 10.1002/aja.1001570107
Doyle DG.During an electron and light microscopic study of the equine intestinal epithelium, it was observed that some secretory granules of the undifferentiated crypt epithelium were incorporated into the nucleus during mitosis. A study was made of the chemical nature of the granules, using standard histochemical techniques: PAS-Alcian blue, Deamination-PAS, and Ninhydrin-Schiff reactions. The granules contained a neutral protein-polysaccharide complex with many terminal amino groups, possibly an antibody (IgA). The intranuclear granules underwent coalescence and degeneration during differentiation. T...
Cell-mediated immunity in horses with sarcoid tumors against sarcoid cells in vitro.
American journal of veterinary research    December 1, 1979   Volume 40, Issue 12 1701-1706 
Broström H, Bredberg-Rådén U, England J, Obel N, Perlmann P.Cell-mediated immunity in horses with sarcoid tumor against sarcoid antigens was studied in vitro by means of mixed lymphocyte tumor cell culture assay and lymphocyte-mediated cytotoxicity of 52Cr-labeled target cells. When Mc-1 sarcoid cells were used as stimulatory cells for peripheral blood lymphocytes in the mixed lymphocyte tumor cell assay, a clear difference in the kinetics of the generated lymphocytic proliferative response could be detected between sarcoid and control horses. With sarcoid horses, their proliferative maximum was reached 3 days earlier than that of the control horses, a...
Lipoproteins as substitutes for serum in Mycoplasma culture medium.
Journal of clinical microbiology    October 1, 1979   Volume 10, Issue 4 586-589 doi: 10.1128/jcm.10.4.586-589.1979
Washburn LR, Somerson NL.Crude lipoprotein-containing fractions obtained from sera of three different animal species were tested, in combination with bovine serum in Mycoplasma pneumoniae culture medium. All sera yielded at least one lipoprotein-containing component which was considerably more effective in promoting mycoplasma growth than the unfractionated serum sample from which it was derived. The very low activity of certain whole-serum samples tested in this investigation suggests that toxic substances may be present in whole serum which are not contained in the lipoprotein preparations. The greatest activity app...
Proliferation and morphology of chick embryo cells cultured in the presence of horse serum and hemoglobin.
In vitro    August 1, 1979   Volume 15, Issue 8 587-592 doi: 10.1007/BF02623394
Verger C.We have shown previously that hemoglobin greatly stimulates chick embryo cell proliferation in Eagle's minimal essential medium supplemented with horse serum. In the present study we compared the effects of horse serum plus 10 micrometers hemoglobin to those of fetal bovine serum on subcultures of chick embryo cells serially propagated at high cell densities. The cells became elongated in the presence of fetal bovine serum and their rate of proliferation progressively decreased, whereas they became polygonal in the presence of horse serum plus hemoglobin and proliferated well in successive cel...
Collagenase in equine cell culture preparation.
Journal of clinical microbiology    June 1, 1979   Volume 9, Issue 6 731-733 doi: 10.1128/jcm.9.6.731-733.1979
Lang G.Equine kidney cells disaggregated by treatment with 0.01% collagenase were used in the preparation of primary monolayer cell cultures. The primary cells could be stored for long periods in liquid nitrogen and subsequently subcultivated. These techniques provided a long-term supply of equine kidney cells, free of apparent contamination, from the kidneys of a single fetus.
In vitro effects of phenylbutazone on equine chromosomes.
The Veterinary record    March 3, 1979   Volume 104, Issue 9 195-196 doi: 10.1136/vr.104.9.195
Smith AL, Lodge JR, Link RP.No abstract available
[Strain of horse embryonic lung diploid cells].
Veterinariia    March 1, 1979   Issue 3 42-43 
Pankova GE, Sologub VK, Gololobova MT, Rezova TI.No abstract available
Specific PGF-2 alpha binding by the corpus luteum of the pregnant and non-pregnant mare.
Journal of reproduction and fertility. Supplement    January 1, 1979   Issue 27 421-429 
Vernon MW, Strauss S, Simonelli M, Zavy MT, Sharp DC.The binding of prostaglandin (PG) F-2 alpha to corpora lutea (CL) from pregnant and non-pregnant Pony mares was examined. Studies of the rates of association and dissociation indicated that [3H]PGF was bound specifically and reversibly to a luteal cell membrane preparation (MP) that was isolated by high speed (100,000 g) ultracentrifugation. Various PGs and PG metabolites displaced [3H]PGF from the receptors in the following decreasing order: PGF-2 alpha greater than 13, 14-dihydro-PGF-2 alpha = 13,14-dihydro-15-keto PGF-2 alpha greater than PGD-2 greater than PGF-1 alpha = PGE-2 greater than ...
Characterization of the infection of equine fibroblasts by equine infectious anemia virus.
Archives of virology    January 1, 1979   Volume 60, Issue 3-4 279-289 doi: 10.1007/BF01317499
Klevjer-Anderson P, Cheevers WP, Crawford TB.Equine dermal fibroblasts persistently infected with equine infectious anemia virus (EIAV) show no alterations in cell morphology or growth kinetics when compared to uninfected cells. The percentage of cells immunofluorescent positive for viral proteins fluctuated, depending upon the stage of the cell cycle, while production of extracellular virus was uniform throughout the cell cycle, increasing only as the cell number increased. This was shown in log versus stationary phase cultures as well as in cultures synchronized by sterum starvation. The establishment of productive infection did not re...
Oestrogens and androgens in blastocoelic fluid and cultures of cells from equine conceptuses of 10-22 days gestation.
Journal of reproduction and fertility. Supplement    January 1, 1979   Issue 27 413-420 
Flood PF, Betteridge KJ, Irvine DS.Six samples of blastocoele fluid recovered between 10 and 22 days gestation were tested in human clinical radioimmunoassay systems measuring total oestrogens and total androgens. The results were erratic but in 5 cases measurements for oestrogen equivalent to between 1000 and 70,000 pg/ml and for androgen between 1000 and 85,000 pg/ml were recorded. Cells from two blastocysts were cultured in medium 199 with and without horse serum. When the used media were assayed, values equivalent to at least 8000 pg oestrogen/ml were obtained on 7 of 11 occasions. In 9 of 11 samples the androgen concentrat...
[Complement fixation reaction studies in rhinopneumonitis of horses].
Veterinarno-meditsinski nauki    January 1, 1979   Volume 16, Issue 8 78-84 
Tatarov G, Martinov S, Panova M.It was established that the complement binding reaction (CBR) is a suitable and very fast method for horse rhino-pneumonitis diagnostics. Cell cultural virus produced in cell cultures of pig kidneys was used as antigen. The antigen lots tested have no anticomplementary properties. Highest complement binding activity was evident in the non-diluted antigen, which discovered specific antibodies in immune serums. The CBR specificity was tested by the aid of homologous and heterologous serums and antigens. The titers of complement binding antibodies in the serums of 255 horses recovered from the di...
A rapid and simple method for the isolation of pure eosinophilic leukocytes from horse blood.
Experientia    December 15, 1978   Volume 34, Issue 12 1654-1656 doi: 10.1007/BF02034734
Jörg A, Portmann P, Fellay G, Dreyer JL, Meyer J.An improved and short method is described for the isolation of intact eosinophilic leukocytes from horse blood with high yield (1--1.5 g/20 l). Viability and purity of the preparations were verified by light and electron microscopy and by the trypan blue exclusion test. Isolated eosinophils were 98--100% pure, intact and viable, and they could be shown to phagocytise immune-complexes.
Glucose transport by horse kidney brush borders. I.–Transport properties of brush border membrane closed vesicles.
Biochimie    September 29, 1978   Volume 60, Issue 6-7 645-651 doi: 10.1016/s0300-9084(78)80783-4
Poirée JC, Vannier C, Sudaka P, Fehlmann M.Brush border membranes isolated from horse kidney cortex as closed right-side out vesicles show selective permeability when analyzed on sucrose and dextran gradients. These vesicles can actively accumulate D-glucose. The preservation of the glucose transport system is demonstrated by the following features: (a) the uptake and release rates of D-glucose are higher in the presence of a sodium gradient, showing that D-glucose transport is a sodium-dependent process; (b) this transport, specific for the D-isomer, is inhibited by phlorizin; (c) the D-glucose transport system is saturable; (d) no in...
Pathogenicity of equine herpesvirus: in vivo persistence in equine tissue macrophages of herpesviuus type 2 detected in monolayer macrophage cell culture.
American journal of veterinary research    September 1, 1978   Volume 39, Issue 9 1422-1427 
Dutta SK, Campbell DL.Equine macrophages from the mammary glands of a yearling filly and an 18-year-old barren nonlactatind mare formed cell monolayers in continuous cultures. There was absence of viral cytopathic effect (CPE) in early cell culture passages. The cells from the early cell culture passages having no CPE failed to show evidence of virus or viral antigen by electron microscopic and immunofluorescence studies. Foci of CPE first appeared in the monolayer cell cultures from the filly and the mare in the 3rd and the 4th serial passages respectively, and the CPE increased on subsequent serial passages. Equi...
Growth of the contagious equine metritis organism in a liquid medium.
The Veterinary record    August 26, 1978   Volume 103, Issue 9 187-188 doi: 10.1136/vr.103.9.187
Fernie DS.No abstract available
Perinatal foal mortality associated with a herpesvirus.
Australian veterinary journal    March 1, 1978   Volume 54, Issue 3 103-105 doi: 10.1111/j.1751-0813.1978.tb05512.x
Dixon RJ, Hartley WJ, Hutchins DR, Lepherd EE, Feilen C, Jones RF, Love DN, Sabine M, Wells AL.An outbreak of perinatal foal mortality associated with a herpesvirus is described. Twenty two foals either were still-born, or died soon after birth, or were weak and soon developed severe respiratory signs, or were normal at birth and developed respiratory symptoms 18 to 24 hours later. Elevated temperatures, heart and respiratory rates were constant features. The animals were severely leucopaenic, and showed an absolute neutropaenia. At autopsy the lungs were enlarged, and showed varying degrees of aeration and moderate to severe oedema and congestion. Histopathology showed an acute focal n...
Microculture method for mixed lymphocyte cultures in the horse.
American journal of veterinary research    February 1, 1978   Volume 39, Issue 2 337-339 
McClure JJ, Muscoplat CC, Johnson DW, Senogles DR.A miniaturized method for the mixed lymphocyte culture test in the horse is described. The test is performed in either round- or flat-bottom microtitration tissue culture plates. Concentrations of responsing and stimulating cells are varied, depening on the experiment. Significant discrimination between isogeneic and allogenic mixtures is possible after 120 hours' culture when cells are labeled ([3H]thymidine) for the last 16 to 18 hours of the test.
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