Dermacentor andersoni: Salivary Gland Proteins Suppressing T-Lymphocyte Responses to Concanavalin A in Vitro

1995 ◽  
Vol 81 (3) ◽  
pp. 262-271 ◽  
Author(s):  
D.K. Bergman ◽  
R.N. Ramachandra ◽  
S.K. Wikel
1980 ◽  
Vol 152 (6) ◽  
pp. 1805-1810 ◽  
Author(s):  
J P Lake ◽  
M E Andrew ◽  
C W Pierce ◽  
T J Braciale

The in vitro secondary cytotoxic T lymphocyte (CTL) response to Sendai virus-treated stimulator cells by primed spleen cells from thymus gland-grafted nude mice was examined. BALB/c (H-2d) nude mice grafted with allogeneic C57BL/10 (H-2b) thymus glands developed CTL responses directed exclusively to Sendai virus-infected H-2d target cells. (C57BL/6 X BALB/c)F1 nude mice grafted with thymus glands of either parent developed CTL responses preferentially against infected target cells expressing the MHC antigens present in the parental thymus graft, but also had detectable activity for infected target cells of the parental haplotype not expressed in the thymus. These results provide evidence against the concept that self recognition by MHC-restricted CTL is directed exclusively by the MCH type of the thymus.


1985 ◽  
Vol 24 (2) ◽  
pp. 260-266 ◽  
Author(s):  
Kathleen E. Rodgers ◽  
Marcia H. Grayson ◽  
Toshiko Imamura ◽  
Bruce H. Devens

2003 ◽  
Vol 222 (2) ◽  
pp. 116-125 ◽  
Author(s):  
Regis Mariano Andrade ◽  
Geisy Monteiro Almeida ◽  
George Alexandre DosReis ◽  
Cleonice Alves Melo Bento

1988 ◽  
Vol 111 (1) ◽  
pp. 39-54 ◽  
Author(s):  
Henry L. Wong ◽  
Darien E. Wilson ◽  
James C. Jenson ◽  
Philip C. Familletti ◽  
Donna L. Stremlo ◽  
...  

1973 ◽  
Vol 58 (2) ◽  
pp. 549-564
Author(s):  
W. R. KAUFMAN ◽  
J. E. PHILLIPS

1. The salivary gland of the ixodid tick, Dermacentor andersoni, can be induced to secrete fluid for at least 6 h when bathed in an artificial medium in vitro. 2. Fluid secretion appears to be a consequence of active Cl secretion since (a) it is inhibited by 95% when nitrate and by 100% when acetate replaces Cl in the bathing medium; however, bromide can support secretion as well as Cl, (b) the rates of fluid and Cl secretion are linearly related to the concentration of Cl in the medium; and (c) the S/H ratio for Cl is greater than unity at all concentrations despite a transacinar P.D. of 35 mV (lumen negative). 3. Although (in the presence of Na) a low concentration of K in the bathing medium stimulates the rate of fluid secretion fivefold, higher concentrations of K inhibit fluid secretion. The latter is largely due to a direct effect of K ion and not simply to increased osmotic pressure or reduced Na concentration. Fluid secretion is completely in hibited by 10-6 M ouabain. On the basis of these observations we propose that fluid secretion may be dependent on a Na-K activated ‘pump ATPase’, which is somehow involved in cation secretion. The S/H ratios of Na and K are greater than unity at all medium concentrations. 4. The saliva secreted in vitro is slightly hypo-osmotic to the bathing medium over a wide range of medium concentration (300-920 mOsm/l). We postulate that the primary saliva is iso- or hyper-osmotic to the bathing medium; the final elaborated saliva is probably rendered hypo-osmotic by a process of solute reabsorption somewhere between the acini and the orifice of the main salivary duct.


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