Open Access
Theranostics, volume 10, issue 23, pages 10743-10768
Mast cells as a unique hematopoietic lineage and cell system: From Paul Ehrlich's visions to precision medicine concepts
P. Valent
1
,
C. V. Akin
2
,
Karin Hartmann
3
,
G. E. NILSSON
4
,
A. Reiter
5
,
Olivier Hermine
6
,
Karl Sotlar
7
,
Wolfgang R Sperr
1
,
Luis Escribano
8
,
Tracy I. George
9
,
Hanneke C. Kluin-Nelemans
10
,
Celalettin Ustun
11
,
M Triggiani
12
,
Knut Brockow
13
,
Jason Gotlib
14
,
Alberto Orfao
8
,
Petri T. Kovanen
15
,
Emir Hadzijusufovic
1, 16
,
Irina Sadovnik
1
,
Hans-Peter Horny
17
,
M. Arock
18
,
Lawrence M. Schwartz
19
,
K. FRANK AUSTEN
20
,
Dean D. Metcalfe
21
,
Stephen J Galli
22
2
15
Wihuri Res Inst, Wihuri Research Institute
Publication type: Journal Article
Publication date: 2020-09-08
Medicine (miscellaneous)
Pharmacology, Toxicology and Pharmaceutics (miscellaneous)
Abstract
The origin and functions of mast cells (MCs) have been debated since their description by Paul Ehrlich in 1879. MCs have long been considered 'reactive bystanders' and 'amplifiers' in inflammatory processes, allergic reactions, and host responses to infectious diseases. However, knowledge about the origin, phenotypes and functions of MCs has increased substantially over the past 50 years. MCs are now known to be derived from multipotent hematopoietic progenitors, which, through a process of differentiation and maturation, form a unique hematopoietic lineage residing in multiple organs. In particular, MCs are distinguishable from basophils and other hematopoietic cells by their unique phenotype, origin(s), and spectrum of functions, both in innate and adaptive immune responses and in other settings. The concept of a unique MC lineage is further supported by the development of a distinct group of neoplasms, collectively referred to as mastocytosis, in which MC precursors expand as clonal cells. The clinical consequences of the expansion and/or activation of MCs are best established in mastocytosis and in allergic inflammation. However, MCs have also been implicated as important participants in a number of additional pathologic conditions and physiological processes. In this article, we review concepts regarding MC development, factors controlling MC expansion and activation, and some of the fundamental roles MCs may play in both health and disease. We also discuss new concepts for suppressing MC expansion and/or activation using molecularly-targeted drugs.
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