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October 5, 2011 marks "Stem Cell Awareness Day," a day recognized by organizations and individuals around the world to promote greater understanding about the importance of stem cell research and its potential applications for treating human disease and injury. This year, NYSTEM sponsored its third annual stem cell image contest. Many visually captivating and scientifically significant stem cell images were submitted by New York stem cell scientists. Selected images are featured in the NYSTEM 2012 calendar (right).

This is a wholemount staining of an adult CD1 mouse backskin at postnatal day 56. This mouse carries a K14-H2BGFP transgene, so all epithelial cells express H2BGFP. The skin was treated with collagenase to get rid of the dermis and the remaining epithelial cells were stained with anti-CD34 (red). CD34 is the marker of hair follicle stem cells in the skin. Blue is the DAPI staining which also highlights the hair shaft. This image was generated by 3D projection of a series of Z stack images taken by a confocal microscopy.
Ting Chen and Elaine Fuchs, The Rockefeller University, New York, NY

Chromatin is visualized by Hoechst. The microtubule cytoskeleton is stained with anti tubulin antibody and shown in green. Several cells undergoing mitotic division of chromosomes are present in this field.
Martin Tomov and Janet Paluh, University at Albany, Albany, NY

The embryonic endoderm contains the stem cells of the respiratory and digestive tracts and associated organs, such as lungs, liver and pancreas. It comprises cells of two origins: pluripotent epiblast (red) and visceral endoderm (green). Ventral view of a mouse embryo depicting the endoderm layer.
Kat Hadjantonakis, Sloan-Kettering institute, New York, NY

The nestin-positive cells isolated from a metastatic prostate cancer patient and grown under stemness-promoting conditions (short-term collagen type I adherent culture in serum-free stem cell medium).
Galina I Botchkina, Stony Brook University Medical Center, Stony Brook, NY
Natalia Peunova, Cold Spring Harbor Laboratory, Cold Spring Harbor, NY

Activated STAT, a transcription factor, is red; negatively-marked FRT82B clones lack GFP (green); and gamma-tubulin, which marks the centromere, is blue. Germline stem cells express high levels of activated STAT (red) surround the niche (not labeled). Yellow cells are somatic stem cells that are positive for STAT (red) and are wild-type for the clone marker (GFP).
Marc Amoyel and Erika Bach, New York University School of Medicine, New York, NY

Mesenchymal progenitor cells are capable of multilineage differentiation into bone, cartilage, fat and skeletal muscle. In this experiment, human embryonic stem cells (H1/WA01) were induced to differentiate into mesenchymal progenitors before purification by flow cytometry. Vimentin protein (dark blue) is characteristic of purified mesenchymal progenitors; the nuclei are counterstained with DAPI (blue-green).
Natalia Novoa and Mark J. Tomishima, Sloan-Kettering Institute, New York, NY

Human induced Pluripotent Stem (iPS) cells were differentiated in vitro to form 3D cellular aggregates called embryoid bodies (EBs) comprising of all three germ layers. A spontaneously beating EB was immunostained using anti-Actinin antibody to label individual cardiomyocytes (green fluorescent) and all the cells were counterstained using Propidium Iodide that labels their nuclei (red fluorescent). The image was acquired by laser scanning confocal microscopy.
Mayurika Desai and Charles Antzelevitch, Masonic Medical Research Laboratory, Utica, NY

Oligodendrocytes derived from human embryonic stem cells (hES) expressing O4 surface antigen (red). The cell nuclei are labeled with DAPI (blue). Newly developed protocols allow the derivation of oligodendrocyte progenitors from hES cells and their maturation into functional cells capable of myelinating the Central Nervous System (CNS).
Tamara Major and Viviane Tabar, Memorial-Sloan Kettering Cancer Center, New York, NY

A human C27 iPS-derived astrocyte in culture: DAPI staining for cell nucleus (blue) and glial fibrillary acidic protein (green).
Devin Chandler-Militello and Steven Goldman, University of Rochester Medical Center, Rochester, NY

Human embryonic stem cells that carry an endothelial specific reporter transgene are differentiated in conditions that foster vascular specification. The image depicts vascular foci comprised of thousands of endothelial cells in a VEGR2-GFP transgenic mouse.
Daylon James and Shahin Rafii, Weill Cornell Medical College, New York, NY

HMSC build a group consensus in response to extracellular matrix mediated stress. The behavior of the group in a particular microenvironment helps dictate hMSC functions and guide differentiation. The f-actin cytoskeleton is stained with phalloidin 488 (red) and the nuclei are stained with sytox orange (green). Images were collected using a Zeiss Confocal Microscope at 40X.
Kira Henderson and George Plopper, Rensselaer Polytechnic Institute, Rensselaer, NY

RPE are multipotent and in defined conditions can readily and reproducibly generate ectodermal and mesodermal lineages. This plasticity may explain human pathologies attributed to the RPE, including heterotopic ocular ossification and anomalous intraocular adipogenic deposits. This image describes human fetal RPE differentiating toward the adipocyte lineage. Illustrating the cells transition are the pigment (evidence of RPE identity), ZO-1 staining (hallmark of an epithelium) in red, and LipoTox TM (an adipocyte marker) in green.
Enrique Salero, Timothy A Blenkinsop, and Barbara Corneo, Neural Stem Cell Institute, Regenerative Research Foundation, Rensselaer, NY

Human endothelial cell lineage on a micropatterned ring (inner diameter: 250 µm, width: 200 µm) stained for actin (red), tubulin (green), and nuclei (blue). Cells form a 'rightward' chiral alignment, while polarized by positioning their centrosomes (bright green) rather than cell nuclei closer to each boundary. This is the first image revealing that individual cells have intrinsic invariant chirality, which depends on cell phenotype. Such a microfabrication-based platform can be potentially used to study the initiation of the left-right asymmetry of life, diagnose disease, and study factors involved with birth malformations.
Leo Q Wan and Gordana Vunjak-Novakovic, Columbia University, New York, NY