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Stress-associated erythropoiesis initiation is regulated by type 1 conventional dendritic cells
Taeg S. Kim, … , Paul C. Trampont, Thomas J. Braciale
Taeg S. Kim, … , Paul C. Trampont, Thomas J. Braciale
Published September 21, 2015
Citation Information: J Clin Invest. 2015;125(10):3965-3980. https://doi.org/10.1172/JCI81919.
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Research Article Immunology

Stress-associated erythropoiesis initiation is regulated by type 1 conventional dendritic cells

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Abstract

Erythropoiesis is an important response to certain types of stress, including hypoxia, hemorrhage, bone marrow suppression, and anemia, that result in inadequate tissue oxygenation. This stress-induced erythropoiesis is distinct from basal red blood cell generation; however, neither the cellular nor the molecular factors that regulate this process are fully understood. Here, we report that type 1 conventional dendritic cells (cDC1s), which are defined by expression of CD8α in the mouse and XCR1 and CLEC9 in humans, are critical for induction of erythropoiesis in response to stress. Specifically, using murine models, we determined that engagement of a stress sensor, CD24, on cDC1s upregulates expression of the Kit ligand stem cell factor on these cells. The increased expression of stem cell factor resulted in Kit-mediated proliferative expansion of early erythroid progenitors and, ultimately, transient reticulocytosis in the circulation. Moreover, this stress response was triggered in part by alarmin recognition and was blunted in CD24 sensor– and CD8α+ DC-deficient animals. The contribution of the cDC1 subset to the initiation of stress erythropoiesis was distinct from the well-recognized role of macrophages in supporting late erythroid maturation. Together, these findings offer insight into the mechanism of stress erythropoiesis and into disorders of erythrocyte generation associated with stress.

Authors

Taeg S. Kim, Mark Hanak, Paul C. Trampont, Thomas J. Braciale

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Figure 9

SCF production by human XCR1+CLEC9A+ DCs in response to CD24 engagement in vitro.

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SCF production by human XCR1+CLEC9A+ DCs in response to CD24 engagement ...
(A and B) Human BDCA3+ (XCR1+CLEC9A+) DCs were identified from fresh human BM aspirates. Surface expression of CD24 by this fresh DC subset was analyzed (A). BM cells were incubated overnight with 2 different monoclonal Abs to human CD24 (αhCD24), eBioSN3 and ML5, and the expression of human mSCF by XCR1+CLEC9A+ DCs was examined (B). Data shown in A and B represent at least 3 independent experiments. (C and D) Human BMDCs were generated from human BM aspirates. Expression of SCF mRNA by human BMDCs was examined at day 9 by qRT-PCR (C). Fresh human BM aspirates were FACS sorted into at least 4 subpopulations. The sorted leukocyte populations within the BM were incubated overnight with αhCD24 (clone eBioSN3). Expression of Scf RNA was evaluated after overnight stimulation by qRT-PCR (D). Data in C and D represent mean ± SEM of triplicates of at least 2 independent experiments. *P < 0.05; **P < 0.01 (2-tailed, unpaired Student’s t test).

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