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Chemical Compound Review

Emericid     (2S)-2-[(2R,3R,4S,5S,6R)-2- hydroxy-6-[(1R)...

Synonyms: Lonomycin, AC1L3YCV, LS-88126, 56832-67-8, 58785-63-0, ...
 
 
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Disease relevance of Emericid

  • A new polyether antibiotic, lonomycin, was isolated from the culture of Streptomyces ribosidifcus strain TM-481 [1].
  • Lonomycin shows antimicrobial activity against gram-positive bacteria [1].
  • These studies involving 7 trials totaling 1,680 broiler chicks, have demonstrated that lonomycin at levels of .003125 to .0125% (dependent on species of Eimeria) in the feed is an effective aid in the control of avian coccidiosis in broiler chickens [2].
 

High impact information on Emericid

  • The advantages and dynamic nature of the system are demonstrated by measuring the effects of the calcium ionophore lonomycin and of extracellular ATP on ciliated rabbit trachea [3].
  • These data indicate that TCR zeta-CD3-dependent CD80 and CD86 co-signaling requires Pl3-kinase binding to the CD28pYMNM motif, while phorbol ester and lonomycin can bypass this requirement in CD28 co-stimulation [4].
  • In this study, we have investigated whether CD28-associated Pl3-kinase is required for CD80 and CD86 co-stimulation, as well as in co-signaling that involves different primary signals (i.e. TCR zeta-CD3 versus phorbol ester/lonomycin) [4].
  • By contrast, CD28 mediated co-stimulation involving receptor ligation plus phorbol ester/lonomycin induced IL-2 independent of Pl3-kinase binding to CD28 [4].
  • Second, antigen induced a different pattern of transcription factor binding activities than PMA/lonomycin in DP thymocytes, AP-1 activity being selectively induced by antigen and NF-kappa B by PMA/lonomycin [5].
 

Chemical compound and disease context of Emericid

  • Lonomycin B (II), C44H75O14Na, m.p. 181-182 degrees C, and lonomycin C (III), C43H73O14Na, m.p 186-187 degrees C, were isolated as their sodium salts from the fermentation broth of Streptomyces ribosidificus TM-481 [6].
 

Anatomical context of Emericid

  • We show that stimulation of naive T cells (CD3+ CD45RA+) derived from cord blood by phorbol ester (phorbol-12-myristate-13-acetate: PMA) plus lonomycin induced detection of Types 1, 2 and 0 cells [7].
  • During the acrosome reaction, induced in capacitated spermatozoa by lonomycin, Vn was released into the medium in a calcium-dependent manner [8].
  • Luteolin monoglucuronide was hydrolyzed to free luteolin by beta-glucuronidase released from neutrophils stimulated with lonomycin and Cytocharasine B [9].

References

  1. Isolation of a new polyether antibiotic, lonomycin. Omura, S., Shibata, M., Machida, S., Sawada, J. J. Antibiot. (1976) [Pubmed]
  2. Anticoccidial activity of lonomycin (SQ 12,525) in chicks. Cruthers, L.R., Szanto, J., Linkenheimer, W.H., Maplesden, D.C., Brown, W.E. Poult. Sci. (1978) [Pubmed]
  3. Simultaneous measurement of ciliary beating and intracellular calcium. Korngreen, A., Priel, Z. Biophys. J. (1994) [Pubmed]
  4. CD28 co-stimulatory regimes differ in their dependence on phosphatidylinositol 3-kinase: common co-signals induced by CD80 and CD86. Cefai, D., Cai, Y.C., Hu, H., Rudd, C. Int. Immunol. (1996) [Pubmed]
  5. Developmental control of antigen-induced thymic transcription factors. Simon, A.K., Auphan, N., Schmitt-Verhulst, A.M. Int. Immunol. (1996) [Pubmed]
  6. Lonomycins B and C, two new components of polyether antibiotics. Fermentation, isolation and characterization. Mizutani, T., Yamagishi, M., Hara, H., Omura, S., Ozeki, M., Mizoue, K., Seto, H., Otake, N. J. Antibiot. (1980) [Pubmed]
  7. Naive T cells from cord blood have the capacity to make Types 1 and 2 cytokines. Perez-Cruz, I., Fallen, P., Madrigal, J.A., Cohen, S.B. Immunol. Lett. (2000) [Pubmed]
  8. Vitronectin is an intrinsic protein of human spermatozoa released during the acrosome reaction. Fusi, F.M., Lorenzetti, I., Mangili, F., Herr, J.C., Freemerman, A.J., Gailit, J., Bronson, R.A. Mol. Reprod. Dev. (1994) [Pubmed]
  9. Metabolic fate of luteolin and its functional activity at focal site. Shimoi, K., Saka, N., Kaji, K., Nozawa, R., Kinae, N. Biofactors (2000) [Pubmed]
 
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