Figure 6 - MC expression of Ntsr1 is required for optimal MC-dependent reduction of NT-induced hypotension and enhancement of survival after CLP.


From the following article

Neurotensin increases mortality and mast cells reduce neurotensin levels in a mouse model of sepsis

Adrian M Piliponsky, Ching-Cheng Chen, Toshihiko Nishimura, Martin Metz, Eon J Rios, Paul R Dobner, Etsuko Wada, Keiji Wada, Sherma Zacharias, Uma M Mohanasundaram, James D Faix, Magnus Abrink, Gunnar Pejler, Ronald G Pearl, Mindy Tsai & Stephen J Galli

Nature Medicine 14, 392 - 398 (2008) Published online: 30 March 2008

doi:10.1038/nm1738

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(a) PLCs containing 5 times 104 PMCs from C57BL/6, Ntsr1-/- or Ntsr2-/- mice were incubated with NT (10 muM) for 30 min at 37 °C. Results are expressed as the percentage of NT remaining after incubation with cells compared to that in samples of NT incubated in vehicle alone at 37 °C (data were pooled from triplicate determinations in the two independent experiments performed, each of which gave similar results). (b,c) Changes in MAP versus baseline levels (baseline = 0, measured 3 min after injection of 300 mul saline, intraperitoneal) at various times after injection of NT (6 nmol in 300 mul saline, intraperitoneal) (b), and amounts of NT in the peritoneal fluids of these mice at 30 min after NT injection (c), in KitW/W-v mice that had been engrafted intraperitoneally with BMCMCs of C57BL/6-Ntsr1+/+ (n = 7) or -Ntsr1-/- (n = 6) origin. (d) Survival after moderate CLP (ligation of distal one-half of cecum; one puncture with a 22-gauge needle) in KitW/W-v mice that had been engrafted intraperitoneally with BMCMCs of C57BL/6-Ntsr1+/+ (n = 14) or Ntsr1-/- (n = 13) origin.

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