Mast cells (MC), which are tissue-resident cells found widely distributed i
n the body, are derived from primitive hematopoietic cells. MC produce a va
riety of biologically active substances such as histamine, proteases, lipid
derivatives and numerous cytokines and chemokines in response to immunolog
ic or non-immunologic stimuli. Of interest, it has been reported that roden
t MC can also be a source of nitric oxide (NO) derivatives, that they synth
esize spontaneously, or only after activation, depending on their subtype.
This synthesis appears to be under the control of the expression of the ind
ucible isoform of the nitric oxide synthase (iNOS) and of the constitutive
neuronal NOS (nNOS). MC might thus be able to influence the survival and fu
nctions of other types of NO-sensitive cells in close vicinity. Apart from
being a source of NO, MC can also be the target for NO and its derivatives.
Indeed, survival and reactivity of rodent MC is influenced by NO derivativ
es produced by MC themselves or by other cellular elements in close contact
with the MC in tissues. By contrast, the existence of such mechanisms of c
ross-talk between MC and NO remains poorly documented in humans. If evidenc
e are supplied in favor of such relationship, pharmacological modulation by
agents acting at the level of the NO pathway might be of interest in order
to regulate the functions of MC in immunologic, neoplastic, inflammatory a
nd other conditions. (C) 2001 Elsevier Science B.V. All rights reserved.