Low-density star cluster formation: Discovery of a young faint fuzzy on the outskirts of the low-mass spiral galaxy NGC 247

The classical globular clusters found in all galaxy types have half-light radii of rh ~2-4 pc, which have been tied to formation in the dense cores of giant molecular clouds. Some old star clusters have larger sizes, and it is unclear if these represent a fundamentally different mode of low-density star cluster formation. We report the discovery of a rare, young \u27faint fuzzy\u27 star cluster, NGC 247-SC1, on the outskirts of the low-mass spiral galaxy NGC 247 in the nearby Sculptor group, and measure its radial velocity using Keck spectroscopy. We use Hubble Space Telescope imaging to measure the cluster half-light radius of rh ≃ 12 pc and a luminosity of LV ≃ 4 × 105Lθ. We produce a colour-magnitude diagram of cluster stars and compare to theoretical isochrones, finding an age of ≃300 Myr, a metallicity of [Z/H] ~-0.6 and an inferred mass of M∗ ≃ 9 × 104Mθ. The narrow width of blue-loop star magnitudes implies an age spread of ≲50 Myr, while no old red-giant branch stars are found, so SC1 is consistent with hosting a single stellar population, modulo several unexplained bright \u27red straggler\u27 stars. SC1 appears to be surrounded by tidal debris, at the end of an ∼2 kpc long stellar filament that also hosts two low-mass, low-density clusters of a similar age. We explore a link between the formation of these unusual clusters and an external perturbation of their host galaxy, illuminating a possible channel by which some clusters are born with large sizes

CXCR4 identifies transitional bone marrow premonocytes that replenish the mature monocyte pool for peripheral responses

It is well established that Ly6C(hi) monocytes develop from common monocyte progenitors (cMoPs) and reside in the bone marrow (BM) until they are mobilized into the circulation. In our study, we found that BM Ly6C(hi) monocytes are not a homogenous population, as current data would suggest. Using computational analysis approaches to interpret multidimensional datasets, we demonstrate that BM Ly6C(hi) monocytes consist of two distinct subpopulations (CXCR4(hi) and CXCR4(lo) subpopulations) in both mice and humans. Transcriptome studies and in vivo assays revealed functional differences between the two subpopulations. Notably, the CXCR4(hi) subset proliferates and is immobilized in the BM for the replenishment of functionally mature CXCR4(lo) monocytes. We propose that the CXCR4(hi) subset represents a transitional premonocyte population, and that this sequential step of maturation from cMoPs serves to maintain a stable pool of BM monocytes. Additionally, reduced CXCR4 expression on monocytes, upon their exit into the circulation, does not reflect its diminished role in monocyte biology. Specifically, CXCR4 regulates monocyte peripheral cellular activities by governing their circadian oscillations and pulmonary margination, which contributes toward lung injury and sepsis mortality. Together, our study demonstrates the multifaceted role of CXCR4 in defining BM monocyte heterogeneity and in regulating their function in peripheral tissues