The Editorial on the Research Topic
Dendritic Cell and Macrophage nomenclature and classification
Mononuclear phagocytes that include dendritic cells (DCs), monocytes, and macrophages
constitute a group of cell types crucial for the control of pathogens and induction
of immune responses as well as for the support of tissue functions. These properties
make them highly relevant targets for immune therapy, vaccination, and treatment of
autoimmune and inflammatory diseases (1, 2). However, exactly how many cell types
exist in the mononuclear phagocyte system (MPS), or whether they even combine to constitute
a family, has been a matter of contention for many years. Historically, cells of the
MPS have, at one time or another, been referred to as erythrophagocytes, pyrrhol cells,
adventitia cells, rhagiocrine cells, polyblasts, clasmatocytes, and histiocytes (Yona
and Gordon) prior to their current terminology established in 1972 (3). The seminal
discovery of a new cell type termed DCs in the 1970s by the late Ralph Steinman that
were distinct from macrophages added even more complexity in the MPS classification
(4). However, some time passed before DCs were fully accepted as true member of the
MPS. Over time, there was appreciation that there were not just one but multiple DC
subtypes, each with a specialized role (5). So, while a “dendritic-shaped cell that
can process and present antigen to activate naive T cells” was a good initial working
definition (6), it did not take into account the inconsistent observations that other
cells can be dendritic in appearance or activate naive T cells, and that not all “DCs”
are immunostimulatory nor dendritic (7). As a result, many different cell types have
been given a DC moniker over the years, such as monocyte-derived DCs, conventional
DCs (cDCs), and plasmacytoid DCs (8). This appreciation of multiple subtypes has both
clarified and confused the field. Importantly, we do not consider the classification
and nomenclature issues as trivial semantics. Indeed, classification is of very practical
importance in allowing researchers to work to a common framework as highlighted by
Norma Lang “If we cannot name it, we cannot control it, finance it, teach it, research
it, or put into public policy (page 109)” (9).
The idea behind this Frontiers Research Topic on “Dendritic Cell and Macrophage Nomenclature
and Classification” was to have an open debate on the advantages and disadvantages
of different classification systems of cells within the MPS. In this Research Topic,
17 contributions from international experts cover the complexity of the MPS, from
its ontogeny and transcriptional regulation, its classification in different tissues
and different species.
First, in a historical perspective, Yona and Gordon examine the early origins and
development of macrophage research from Ilya Metchnikoff’s discovery to the establishment
of the MPS nomenclature half a century ago.
In an opinion article, Vremec and Shortman discuss issues of DC subset definition
encountered in their past work.
In a hypothesis and theory article, Guilliams and van de Laar discuss the practical
application of our recently proposed classification system based on ontogeny (8).
Hoeffel and Ginhoux cover the ontogeny of tissue-resident macrophages and discuss
evidence suggesting that hematopoietic stem cell-independent embryonic precursors
transiently present in the yolk sac and the fetal liver give rise to long-lasting
self-renewing macrophage populations.
Tussiwand and Gautier discuss the developmental pathways of murine MPS cells, with
a particular emphasis on the transcriptional factors that regulate their development
and function.
Poltorak and Schraml review experimental approaches taken to fate map DCs and discuss
how these have shaped our understanding of DC ontogeny and lineage affiliation.
In a perspective article, Gottschalk and Kurts review the complexity of the renal
MPS, and how to distinguish DCs and macrophages in the kidney from the nephrologist’s
point of view.
Gross et al. discuss origins and functions of intestinal DCs and macrophages and their
respective subsets, focusing largely on the mouse and cells residing in the lamina
propria.
Greter et al. discuss myeloid cells in the brain and the difficulties to delineate
resident microglia from infiltrating myeloid cells using currently known markers and
the recent advances that have helped to make clear definitions between phenotypically
similar, yet functionally diverse myeloid cell types of the brain.
Cassado et al. review the heterogeneity of peritoneal macrophages, which exhibit distinct
phenotypes, functions, and origins.
Eckert et al. summarize the multiple roles of macrophages and DCs in chronic liver
diseases and outline the currently known marker combinations for the identification
of these cell populations for the study of their role in liver immunology.
Moving to human cells, Reynolds and Haniffa review the parallel organization of human
and mouse mononuclear phagocyte networks. They also discuss the strategies, power,
and utility of comparative biology approaches to integrate recent advances in human
and mouse mononuclear phagocyte biology, and its potential to drive forward clinical
translation of this knowledge.
In a research article, Vu-Manh et al. extend our knowledge of the homology of the
MPS across species through comparative transcriptomics. They present an approach combining
refined cell sorting and integrated comparative transcriptomics analyses, which revealed
conservation of the mononuclear phagocyte organization across human, mouse, sheep,
pigs, and chicken.
In a complementary review, Vu-Manh et al. discuss the highly significant conservation
during evolution of DC subsets cell surface phenotyping, expression analysis of hallmark
genes, and functions.
Ziegler-Heitbrock reviews human blood monocyte heterogeneity and their subdivision
into classical, intermediate, and non-classical monocytes, and how these proportions
change during inflammation and discuss its relevance to management of disease.
Durand and Segura review recent advances in our understanding of the human DC network
and discuss some remaining gaps and future challenges of the human DC field.
Finally, in an original research article, Sudan et al. identify novel markers of activated
human macrophages through the analysis of gene-expression profiles for human macrophages
of a single donor subjected to 33 distinct activating conditions.
Altogether, the many contributions to this Frontiers Research Topic not only underline
the complexity of the MPS system but also highlight the similarities between MPS cells
of different tissues. Moreover, classifying MPS cells based on their gene-expression
profiles results in a classification system that is close to the classification of
cells based on their cellular origin and development. Although a final basis for MPS
classification has not been defined yet, we hope this Frontiers Research Topic will
pave the way toward a wider consensus within the field.
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial
or financial relationships that could be construed as a potential conflict of interest.