Amplification of immunoglobulin lambda constant genes in populations of wild mice

The lambda immunoglobulin light chain (Ig lambda) locus of BALB/c inbred mice consists of two variable region gene segments (V lambda)1-3, and four constant region gene segments (C lambda)1,2,4,5. Each C lambda gene segment is associated with a unique joining segment (J lambda)2,4-7, and they are organized in two paired units, J3C3-J1C1 and J2C2-J4C4 (refs 4, 8). Using cDNA probes specific for C lambda 1 and C lambda 2 (ref. 9) we have analysed the genomic organization of the C lambda gene segments in wild-derived and inbred strains of mice. Although Southern blots of the genomic DNA of inbred mice show a constant pattern of hybridization, wild-derived mice show a high degree of variation in the number, size and intensity of hybridizing fragments. We have now found that, per haploid genome, mice of a Mus musculus musculus stock isolated from Sladeckovce, Czechoslovakia (CzII) have at least 12 C lambda segments, and mice of a Mus musculus domesticus stock 'Centreville Lights' from Centreville, Maryland (CL) have at least 8 C lambda segments. There appears to have been relatively recent amplifications of the C lambda gene segments in wild mice.     

Effects of monosodium glutamate on circulating concentrations of luteinizing hormone and growth hormone in young growing domestic fowl (Gallus domesticus)

Summary The administration of monosodium glutamate (MSG) at a dose of 4 g/kg in 5-day-old fowl or 5 daily injections of MSG (total dose 20 g/kg) in 1- to 5-day-old fowl did not affect body growth in either male or female domestic fowl. Neither MSG treatment schedule affected either testis weight or the circulating concentration of luteinizing hormone (LH). A small, but significant decrease in the plasma concentration of growth hormone (GH) was observed in female chicks which had received daily MSG injections.Acknowledgments. Paper of Journal Series, New Jersey State Experiment Station, project No. 18141 and 18443, supported by State and Hatch Act funds and grants from the National Science Foundation (PCM 80227227) and the Upjohn Company.     

Effects of precocene II and juvenile hormone III on the activity of neurosecretory A-cells inOncopeltus fasciatus

Summary Application of precocene II, topically or by contact method, appears to inhibit the synthetic activity of neurosecretory A-cells of the pars intercerebralis ofOncopeltus fasciatus. Treatment of precocene-treated insects with JH III apparently stimulates the secretory activity of these cells.Supported by National Research Council of Canada grant No. A4669.We thank Dr G. B. Staal, Zoecon Corporation, Palo Alto, California, for the gift of precocene II.     

Comparison of the localization of several muscle proteins in relaxed and contracted myofibrils.

The localization of several muscle proteins in relaxed and contracted myofibrils is compared. The morphology of the myofibrils and the behavior of these proteins was also investigated under extraction conditions.     

Modification of clonazepam anticonvulsive activity by its association with other anti-epileptic drugs

Summary The modification of the anti-epileptic activity of clonazepam by other anticonvulsivants is studied. The results vary according to the drug and technique used. The usefulness of the 2 techniques employed is discussed.     

A simple procedure for removal of intra- and extra-tumoral macrophages from primary tumor cultures

Summary Improved growth of tumor cells in primary cell suspensions isolated from solid tumors can be achieved by addition of an antifungal agent, mycostatin, to the culture medium. Mycostatin inhibits the cytotoxicity of macrophages and also quickly detaches phagocytes without any apparent retardation of the growth of tumor cells. This method is particularly useful for obtaining cultures of lung tumor cells or cells from lung metastases of other tumors.This research was supported in part by grants CA-22839 and CA-28482 awarded by the National Cancer Institute, DHEW, USA. This is publication No. 406 from the Department of Basic and Clinical Immunology and Microbiology, Medical University of South Carolina.We thank Charles L. Smith for editorial assistance. Address correspondence to Y. Y., Department of Basic and Clinical Immunology and Microbiology, Medical University of South Carolina, 171 Ashley Avenue, Charleston, SC 29403, USA.