Inducible pluripotent stem cells to study human mast cell trajectories.

Mast cells (MCs) are derived from CD34 hematopoietic progenitors, consist of different subtypes, and are involved in several inflammatory conditions. However, our understanding of human MC developmental trajectories and subtypes has been limited by a scarcity of suitable cellular model systems. Herein, we developed an in vitro model of human MC differentiation from induced pluripotent stem cells (iPSC) to study human MC differentiation trajectories. Flow cytometry characterization of hemopoietic cells derived from the myeloid cells-forming complex (MCFC) revealed an initial increase in Lin CD34 hematopoietic progenitors within Weeks 1-3, followed by an increase in CD34 CD45RA SSC and SSC hematopoietic cells. The Lin CD34 hematopoietic progenitors consisted of SSC CD45RA CD123 c-Kit FcεRI populations that were β7-integrin CD203c and β7-integrin CD203c cells consistent with CMP cells. Flow cytometry and cytologic analyses of the CD34 Lin (SSC) population revealed hypogranular cell populations, predominantly characterized by CD45RA CD123 c-Kit FcεRI β7-integrin and CD45RA CD123 c-Kit FcεRI β7-integrin cells. Analyses of hypergranular SSC cells identified Lin CD34 CD45RA c-Kit FcεRI and Lin CD34 CD45RA c-Kit FcεRI cells. scRNA-seq analysis of the cells harvested at week 4 of the MCFC culture revealed the presence of monocyte and granulocyte progenitors (n = 547 cells, 26.7 %), Erythrocyte / unknown (n = 85, 4.1 %), neutrophils / myelocytes (n = 211 cells, 10.2 %), mast cell progenitor 1 (n = 599, 29.1 %), mast cell progenitor 2 (n = 152, 7.4 %), committed mast cell precursor (n = 113, 5.5 %), and MCs (n = 353, 17.1 %). In silico analyses of the MC precursor and mature MC populations revealed transcriptionally distinct MC precursor subtype and mature MC states (CMA1 and CMA1 subtypes). Culturing MC precursor populations in MC maturation media (mast cell media II) led to homogenous mature MC populations as evidenced by high expression of high-affinity IgE receptor, metachromatic granules, presence of MC granule proteins (Tryptase and Chymase) and activation following substance P stimulation and FcεRI crosslinking. This human iPSC-based approach generates MC precursors and phenotypically mature and functional MC populations. This system will be a useful model to generate human MC populations and broaden our understanding of MC biology and transcriptional regulation of MC differentiation trajectories.