Research Gallery

Below are images from the current topics under investigation in the Department of Cell and Developmental Biology. For further information on these and related projects, click on the name below the image to go to that investigator's page in the Upstate Medical University's Faculty Database

From the research of David Mitchell, Ph.D.
Immunofluorescent image of a single Chlamydomonas cell stained for flagellar dynein protein IC2 (green) and intraflagellar transport protein IFT46 (red). The IFT protein, required for dynein assembly, is concentrated at basal bodies and in patches along each flagellum, whereas assembled dynein is evenly distributed on the flagella and unassembled dynein is seen in puncta in the cytoplasm.
Normal Rat Kidney cells
From the research of Christopher E. Turner, Ph.D.
Triple-labeled immunofluorescence image of Normal Rat Kidney cells. Red staining corresponds to the focal adhesion protein paxillin. The actin cytoskeleton is labeled in green and the nuclei are stained blue. Paxillin is a multi-domain adapter protein that provides an important link between the actin cytoskeleton and transmembrane integrin receptors.
From the research of Jean Sanger, Ph.D.
Confocal image of a projection of focal planes through a three day-old embryonic zebrafish heart (ventricle V and atrium A) showing the distribution of the forming myofibrils. Nuclei, stained with DAPI are blue. Actin and myosin were stained with fluorescent phalloidin (red) and myosin antibodies (green).
mouse cortex
From the research of James S. McCasland, Ph.D.
Flattened left hemisphere of GAP-43 wildtype (+/+) mouse cortex immunostained with serotonin transporter (5HT-T). The layer IV thalamocortical afferents show a complete body map: V: visual, A: auditory, a-e: large whiskers, SW: small whiskers, LL: lower lip, FL: forelimb, T: trunk, HL: hindlimb. Reference: PNAS Vol. 96, pp. 9397-9402, August 1999.
Caenorhabditis elegans
From the research of David W. Pruyne, Ph.D
Shown is the head of a Caenorhabditis elegans adult worm expressing the formin, FHOD-1, fused to GFP. The fusion protein shows the formin is expressed in the large pharynx within the head, and in the body wall muscles in the form of small puncta near the surface of the worm's body.
whole mount quail embryo
From the research of Thomas J. Poole, Ph.D.
This is a whole mount quail embryo stained with the QH-1 monoclonal antibody. QH-1 specifically labelsquail endothelial cells and their precursors.
wild-type paxillin cells
wild-type paxillin cells

paxillin lacking LD4 cells
paxillin lacking LD4 cells

Cells expressing wild-type paxillin (top) or paxillin lacking LD4 (bottom) were scratch-wounded followed by fixation 12 hours post-wounding. Tubulin (Green) and alpha-mannosidase II (Red) were labeled to note cell polarization and Golgi orientation. Cells expressing paxillin lacking LD4 are unable to reorient the Golgi towards the wound edge. From the lab of Christopher Turner, PhD.

lab assistant examining bottles