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This is a searchable collection of scientific photos, illustrations, and videos. The images and videos in this gallery are licensed under Creative Commons Attribution Non-Commercial ShareAlike 3.0. This license lets you remix, tweak, and build upon this work non-commercially, as long as you credit and license your new creations under identical terms.
1247: Crab nerve cell
1247: Crab nerve cell
Neuron from a crab showing the cell body (bottom), axon (rope-like extension), and growth cone (top right).
Tina Weatherby Carvalho, University of Hawaii at Manoa
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3632: Developing nerve cells
3632: Developing nerve cells
These developing mouse nerve cells have a nucleus (yellow) surrounded by a cell body, with long extensions called axons and thin branching structures called dendrites. Electrical signals travel from the axon of one cell to the dendrites of another.
This image was part of the Life: Magnified exhibit that ran from June 3, 2014, to January 21, 2015, at Dulles International Airport.
This image was part of the Life: Magnified exhibit that ran from June 3, 2014, to January 21, 2015, at Dulles International Airport.
Torsten Wittmann, University of California, San Francisco
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3743: Developing Arabidopsis flower buds
3743: Developing Arabidopsis flower buds
Flower development is a carefully orchestrated, genetically programmed process that ensures that the male (stamen) and female (pistil) organs form in the right place and at the right time in the flower. In this image of young Arabidopsis flower buds, the gene SUPERMAN (red) is activated at the boundary between the cells destined to form the male and female parts. SUPERMAN activity prevents the central cells, which will ultimately become the female pistil, from activating the gene APETALA3 (green), which induces formation of male flower organs. The goal of this research is to find out how plants maintain cells (called stem cells) that have the potential to develop into any type of cell and how genetic and environmental factors cause stem cells to develop and specialize into different cell types. This work informs future studies in agriculture, medicine and other fields.
Nathanaël Prunet, Caltech
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2683: GFP sperm
2683: GFP sperm
Fruit fly sperm cells glow bright green when they express the gene for green fluorescent protein (GFP).
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3389: NCMIR Intestine-1
3389: NCMIR Intestine-1
The small intestine is where most of our nutrients from the food we eat are absorbed into the bloodstream. The walls of the intestine contain small finger-like projections called villi which increase the organ's surface area, enhancing nutrient absorption. It consists of the duodenum, which connects to the stomach, the jejenum and the ileum, which connects with the large intestine. Related to image 3390.
Tom Deerinck, National Center for Microscopy and Imaging Research (NCMIR)
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1333: Mitosis and meiosis compared
1333: Mitosis and meiosis compared
Meiosis is used to make sperm and egg cells. During meiosis, a cell's chromosomes are copied once, but the cell divides twice. During mitosis, the chromosomes are copied once, and the cell divides once. For simplicity, cells are illustrated with only three pairs of chromosomes. See image 6788 for a labeled version of this illustration.
Judith Stoffer
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2496: Body toxins
2496: Body toxins
Body organs such as the liver and kidneys process chemicals and toxins. These "target" organs are susceptible to damage caused by these substances. See image 2497 for a labeled version of this illustration.
Crabtree + Company
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6550: Time-lapse video of floral pattern in a mixture of two bacterial species, Acinetobacter baylyi and Escherichia coli, grown on a semi-solid agar for 24 hours
6550: Time-lapse video of floral pattern in a mixture of two bacterial species, Acinetobacter baylyi and Escherichia coli, grown on a semi-solid agar for 24 hours
This time-lapse video shows the emergence of a flower-like pattern in a mixture of two bacterial species, motile Acinetobacter baylyi and non-motile Escherichia coli (green), that are grown together for 24 hours on 0.75% agar surface from a small inoculum in the center of a Petri dish.
See 6557 for a photo of this process at 24 hours on 0.75% agar surface.
See 6553 for a photo of this process at 48 hours on 1% agar surface.
See 6555 for another photo of this process at 48 hours on 1% agar surface.
See 6556 for a photo of this process at 72 hours on 0.5% agar surface.
See 6557 for a photo of this process at 24 hours on 0.75% agar surface.
See 6553 for a photo of this process at 48 hours on 1% agar surface.
See 6555 for another photo of this process at 48 hours on 1% agar surface.
See 6556 for a photo of this process at 72 hours on 0.5% agar surface.
L. Xiong et al, eLife 2020;9: e48885
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2428: Colorful cells
2428: Colorful cells
Actin (purple), microtubules (yellow), and nuclei (green) are labeled in these cells by immunofluorescence. This image won first place in the Nikon 2003 Small World photo competition.
Torsten Wittmann, Scripps Research Institute
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1017: Lily mitosis 07
1017: Lily mitosis 07
A light microscope image of a cell from the endosperm of an African globe lily (Scadoxus katherinae). This is one frame of a time-lapse sequence that shows cell division in action. The lily is considered a good organism for studying cell division because its chromosomes are much thicker and easier to see than human ones. Staining shows microtubules in red and chromosomes in blue. Here, condensed chromosomes are clearly visible and have lined up in the middle of the dividing cell.
Related to images 1010, 1011, 1012, 1013, 1014, 1015, 1016, 1018, 1019, and 1021.
Related to images 1010, 1011, 1012, 1013, 1014, 1015, 1016, 1018, 1019, and 1021.
Andrew S. Bajer, University of Oregon, Eugene
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3273: Heart muscle with reprogrammed skin cells
3273: Heart muscle with reprogrammed skin cells
Skins cells were reprogrammed into heart muscle cells. The cells highlighted in green are remaining skin cells. Red indicates a protein that is unique to heart muscle. The technique used to reprogram the skin cells into heart cells could one day be used to mend heart muscle damaged by disease or heart attack. Image and caption information courtesy of the California Institute for Regenerative Medicine.
Deepak Srivastava, Gladstone Institute of Cardiovascular Disease, via CIRM
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5887: Plasma-Derived Membrane Vesicles
5887: Plasma-Derived Membrane Vesicles
This fiery image doesn’t come from inside a bubbling volcano. Instead, it shows animal cells caught in the act of making bubbles, or blebbing. Some cells regularly pinch off parts of their membranes to produce bubbles filled with a mix of proteins and fats. The bubbles (red) are called plasma-derived membrane vesicles, or PMVs, and can travel to other parts of the body where they may aid in cell-cell communication. The University of Texas, Austin, researchers responsible for this photo are exploring ways to use PMVs to deliver medicines to precise locations in the body.
This image, entered in the Biophysical Society’s 2017 Art of Science Image contest, used two-channel spinning disk confocal fluorescence microscopy. It was also featured in the NIH Director’s Blog in May 2017.
This image, entered in the Biophysical Society’s 2017 Art of Science Image contest, used two-channel spinning disk confocal fluorescence microscopy. It was also featured in the NIH Director’s Blog in May 2017.
Jeanne Stachowiak, University of Texas at Austin
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3583: Bee venom toxin destroying a cell
3583: Bee venom toxin destroying a cell
This video condenses 6.5 minutes into less than a minute to show how the toxin in bee venom, called melittin, destroys an animal or bacterial cell. What looks like a red balloon is an artificial cell filled with red dye. Melittin molecules are colored green and float on the cell's surface like twigs on a pond. As melittin accumulates on the cell's membrane, the membrane expands to accommodate it. In the video, the membrane stretches into a column on the left. When melittin levels reach a critical threshold, countless pinhole leaks burst open in the membrane. The cell's vital fluids (red dye in the video) leak out through these pores. Within minutes, the cell collapses.
Huey Huang, Rice University
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3264: Peripheral nerve cell derived from ES cells
3264: Peripheral nerve cell derived from ES cells
A peripheral nerve cell made from human embryonic stem cell-derived neural crest stem cells. The nucleus is shown in blue, and nerve cell proteins peripherin and beta-tubulin (Tuj1) are shown in green and red, respectively. Related to image 3263.
Stephen Dalton, University of Georgia
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1010: Lily mitosis 10
1010: Lily mitosis 10
A light microscope image of a cell from the endosperm of an African globe lily (Scadoxus katherinae). This is one frame of a time-lapse sequence that shows cell division in action. The lily is considered a good organism for studying cell division because its chromosomes are much thicker and easier to see than human ones. Staining shows microtubules in red and chromosomes in blue. Here, condensed chromosomes are clearly visible and are separating to form the cores of two new cells.
Related to images 1011, 1012, 1013, 1014, 1015, 1016, 1017, 1018, 1019, and 1021.
Related to images 1011, 1012, 1013, 1014, 1015, 1016, 1017, 1018, 1019, and 1021.
Andrew S. Bajer, University of Oregon, Eugene
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2607: Mouse embryo showing Smad4 protein
2607: Mouse embryo showing Smad4 protein
This eerily glowing blob isn't an alien or a creature from the deep sea--it's a mouse embryo just eight and a half days old. The green shell and core show a protein called Smad4. In the center, Smad4 is telling certain cells to begin forming the mouse's liver and pancreas. Researchers identified a trio of signaling pathways that help switch on Smad4-making genes, starting immature cells on the path to becoming organs. The research could help biologists learn how to grow human liver and pancreas tissue for research, drug testing and regenerative medicine. In addition to NIGMS, NIH's National Institute of Diabetes and Digestive and Kidney Diseases also supported this work.
Kenneth Zaret, Fox Chase Cancer Center
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3442: Cell division phases in Xenopus frog cells
3442: Cell division phases in Xenopus frog cells
These images show three stages of cell division in Xenopus XL177 cells, which are derived from tadpole epithelial cells. They are (from top): metaphase, anaphase and telophase. The microtubules are green and the chromosomes are blue. Related to 3443.
Claire Walczak, who took them while working as a postdoc in the laboratory of Timothy Mitchison
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3567: RSV-Infected Cell
3567: RSV-Infected Cell
Viral RNA (red) in an RSV-infected cell. More information about the research behind this image can be found in a Biomedical Beat Blog posting from January 2014.
Eric Alonas and Philip Santangelo, Georgia Institute of Technology and Emory University
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1335: Telomerase illustration
1335: Telomerase illustration
Reactivating telomerase in our cells does not appear to be a good way to extend the human lifespan. Cancer cells reactivate telomerase.
Judith Stoffer
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1160: Vibrio bacteria
1160: Vibrio bacteria
Vibrio, a type (genus) of rod-shaped bacteria. Some Vibrio species cause cholera in humans.
Tina Weatherby Carvalho, University of Hawaii at Manoa
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3557: Bioluminescent imaging in adult zebrafish - overhead view
3557: Bioluminescent imaging in adult zebrafish - overhead view
Luciferase-based imaging enables visualization and quantification of internal organs and transplanted cells in live adult zebrafish. In this image, a cardiac muscle-restricted promoter drives firefly luciferase expression.
For imagery of both the lateral and overhead view go to 3556.
For imagery of the lateral view go to 3558.
For more information about the illumated area go to 3559.
For imagery of both the lateral and overhead view go to 3556.
For imagery of the lateral view go to 3558.
For more information about the illumated area go to 3559.
Kenneth Poss, Duke University
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6793: Yeast cells with endocytic actin patches
6793: Yeast cells with endocytic actin patches
Yeast cells with endocytic actin patches (green). These patches help cells take in outside material. When a cell is in interphase, patches concentrate at its ends. During later stages of cell division, patches move to where the cell splits. This image was captured using wide-field microscopy with deconvolution.
Related to images 6791, 6792, 6794, 6797, 6798, and videos 6795 and 6796.
Related to images 6791, 6792, 6794, 6797, 6798, and videos 6795 and 6796.
Alaina Willet, Kathy Gould’s lab, Vanderbilt University.
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3614: Birth of a yeast cell
3614: Birth of a yeast cell
Yeast make bread, beer, and wine. And like us, yeast can reproduce sexually. A mother and father cell fuse and create one large cell that contains four offspring. When environmental conditions are favorable, the offspring are released, as shown here. Yeast are also a popular study subject for scientists. Research on yeast has yielded vast knowledge about basic cellular and molecular biology as well as about myriad human diseases, including colon cancer and various metabolic disorders.
This image was part of the Life: Magnified exhibit that ran from June 3, 2014, to January 21, 2015, at Dulles International Airport.
This image was part of the Life: Magnified exhibit that ran from June 3, 2014, to January 21, 2015, at Dulles International Airport.
Juergen Berger, Max Planck Institute for Developmental Biology, and Maria Langegger, Friedrich Miescher Laboratory of the Max Planck Society, Germany
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6535: Kupffer cell residing in the liver
6535: Kupffer cell residing in the liver
Kupffer cells appear in the liver during the early stages of mammalian development and stay put throughout life to protect liver cells, clean up old red blood cells, and regulate iron levels. Source article Replenishing the Liver’s Immune Protections. Posted on December 12th, 2019 by Dr. Francis Collins.
Thomas Deerinck, National Center for Microscopy and Imaging Research, University of California, San Diego.
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3624: Fibroblasts with nuclei in blue, energy factories in green and the actin cytoskeleton in red
3624: Fibroblasts with nuclei in blue, energy factories in green and the actin cytoskeleton in red
The cells shown here are fibroblasts, one of the most common cells in mammalian connective tissue. These particular cells were taken from a mouse embryo. Scientists used them to test the power of a new microscopy technique that offers vivid views of the inside of a cell. The DNA within the nucleus (blue), mitochondria (green), and actin filaments in the cellular skeleton (red) are clearly visible.
This image was part of the Life: Magnified exhibit that ran from June 3, 2014, to January 21, 2015, at Dulles International Airport.
This image was part of the Life: Magnified exhibit that ran from June 3, 2014, to January 21, 2015, at Dulles International Airport.
Dylan Burnette, NICHD
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3449: Calcium uptake during ATP production in mitochondria
3449: Calcium uptake during ATP production in mitochondria
Living primary mouse embryonic fibroblasts. Mitochondria (green) stained with the mitochondrial membrane potential indicator, rhodamine 123. Nuclei (blue) are stained with DAPI. Caption from a November 26, 2012 news release from U Penn (Penn Medicine).
Lili Guo, Perelman School of Medicine, University of Pennsylvania
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3478: DDR2 Receptors Attach to Collagen in Breast Tumor
3478: DDR2 Receptors Attach to Collagen in Breast Tumor
On the left, the boundary of a breast tumor (yellow) attaches to collagen fibers that are closest to it (green) using DDR2. On the right, a tumor without DDR2 remains disconnected from the collagen.
Callie Corsa and Suzanne Ponik, Washington University School of Medicine in St. Louis
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3263: Peripheral nerve cells derived from ES cells
3263: Peripheral nerve cells derived from ES cells
Peripheral nerve cells made from human embryonic stem cell-derived neural crest stem cells. The nuclei are shown in blue, and nerve cell proteins peripherin and beta-tubulin (Tuj1) are shown in green and red, respectively. Related to image 3264. Image is featured in October 2015 Biomedical Beat blog post Cool Images: A Halloween-Inspired Cell Collection.
Stephen Dalton, University of Georgia
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2725: Supernova bacteria
2725: Supernova bacteria
Bacteria engineered to act as genetic clocks flash in synchrony. Here, a "supernova" burst in a colony of coupled genetic clocks just after reaching critical cell density. Superimposed: A diagram from the notebook of Christiaan Huygens, who first characterized synchronized oscillators in the 17th century.
Jeff Hasty, UCSD
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3289: Smooth muscle from mouse stem cells
3289: Smooth muscle from mouse stem cells
These smooth muscle cells were derived from mouse neural crest stem cells. Red indicates smooth muscle proteins, blue indicates nuclei. Image and caption information courtesy of the California Institute for Regenerative Medicine.
Deepak Srivastava, Gladstone Institutes, via CIRM
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6661: Zebrafish embryo showing vasculature
6661: Zebrafish embryo showing vasculature
A zebrafish embryo. The blue areas are cell bodies, the green lines are blood vessels, and the red glow is blood. This image was created by stitching together five individual images captured with a hyperspectral multipoint confocal fluorescence microscope that was developed at the Eliceiri Lab.
Kevin Eliceiri, University of Wisconsin-Madison.
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2489: Immune cell attacks cell infected with a retrovirus
2489: Immune cell attacks cell infected with a retrovirus
T cells engulf and digest cells displaying markers (or antigens) for retroviruses, such as HIV.
Kristy Whitehouse, science illustrator
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2442: Hydra 06
2442: Hydra 06
Hydra magnipapillata is an invertebrate animal used as a model organism to study developmental questions, for example the formation of the body axis.
Hiroshi Shimizu, National Institute of Genetics in Mishima, Japan
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3718: A Bacillus subtilis biofilm grown in a Petri dish
3718: A Bacillus subtilis biofilm grown in a Petri dish
Bacterial biofilms are tightly knit communities of bacterial cells growing on, for example, solid surfaces, such as in water pipes or on teeth. Here, cells of the bacterium Bacillus subtilis have formed a biofilm in a laboratory culture. Researchers have discovered that the bacterial cells in a biofilm communicate with each other through electrical signals via specialized potassium ion channels to share resources, such as nutrients, with each other. This insight may help scientists to improve sanitation systems to prevent biofilms, which often resist common treatments, from forming and to develop better medicines to combat bacterial infections. See the Biomedical Beat blog post Bacterial Biofilms: A Charged Environment for more information.
Gürol Süel, UCSD
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2807: Vimentin in a quail embryo
2807: Vimentin in a quail embryo
Confocal image showing high levels of the protein vimentin (white) at the edge zone of a quail embryo. Cell nuclei are labeled green. More specifically, this high-magnification (60X) image shows vimentin immunofluorescence in the edge zone (top of image) and inner zone (bottom of image) of a Stage 4 quail blastoderm. Vimentin expression (white) is shown merged with Sytox nuclear labeling (green) at the edge of the blastoderm. A thick vimentin filament runs circumferentially (parallel to the direction of the edge) that appears to delineate the transition between the edge zone and interior zone. Also shown are dense vimentin clusters or foci, which typically appear to be closely associated with edge cell nuclei. An NIGMS grant to Professor Garcia was used to purchase the confocal microscope that collected this image. Related to image 2808 and video 2809.
Andrés Garcia, Georgia Tech
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3434: Flu virus proteins during self-replication
3434: Flu virus proteins during self-replication
Influenza (flu) virus proteins in the act of self-replication. Viral nucleoprotein (blue) encapsidates [encapsulates] the RNA genome (green). The influenza virus polymerase (orange) reads and copies the RNA genome. In the background is an image of influenza virus ribonucleoprotein complexes observed using cryo-electron microscopy. This image is from a November 2012 News Release.
Scripps Research Institute in La Jolla, CA
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6569: Cryo-electron tomography of a Caulobacter bacterium
6569: Cryo-electron tomography of a Caulobacter bacterium
3D image of Caulobacter bacterium with various components highlighted: cell membranes (red and blue), protein shell (green), protein factories known as ribosomes (yellow), and storage granules (orange).
Peter Dahlberg, Stanford University.
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6532: Mosaicism in C. elegans (Black Background)
6532: Mosaicism in C. elegans (Black Background)
In the worm C. elegans, double-stranded RNA made in neurons can silence matching genes in a variety of cell types through the transport of RNA between cells. The head region of three worms that were genetically modified to express a fluorescent protein were imaged and the images were color-coded based on depth. The worm on the left lacks neuronal double-stranded RNA and thus every cell is fluorescent. In the middle worm, the expression of the fluorescent protein is silenced by neuronal double-stranded RNA and thus most cells are not fluorescent. The worm on the right lacks an enzyme that amplifies RNA for silencing. Surprisingly, the identities of the cells that depend on this enzyme for gene silencing are unpredictable. As a result, worms of identical genotype are nevertheless random mosaics for how the function of gene silencing is carried out. For more, see journal article and press release. Related to image 6534.
Snusha Ravikumar, Ph.D., University of Maryland, College Park, and Antony M. Jose, Ph.D., University of Maryland, College Park
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3306: Planarian stem cell colony
3306: Planarian stem cell colony
Planarians are freshwater flatworms that have powerful abilities to regenerate their bodies, which would seem to make them natural model organisms in which to study stem cells. But until recently, scientists had not been able to efficiently find the genes that regulate the planarian stem cell system. In this image, a single stem cell has given rise to a colony of stem cells in a planarian. Proliferating cells are red, and differentiating cells are blue. Quantitatively measuring the size and ratios of these two cell types provides a powerful framework for studying the roles of stem cell regulatory genes in planarians.
Peter Reddien, Whitehead Institute
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6986: Breast cancer cells change migration phenotypes
6986: Breast cancer cells change migration phenotypes
Cancer cells can change their migration phenotype, which includes their shape and the way that they move to invade different tissues. This movie shows breast cancer cells forming a tumor spheroid—a 3D ball of cancer cells—and invading the surrounding tissue. Images were taken using a laser scanning confocal microscope, and artificial intelligence (AI) models were used to segment and classify the images by migration phenotype. On the right side of the video, each phenotype is represented by a different color, as recognized by the AI program based on identifiable characteristics of those phenotypes. The movie demonstrates how cancer cells can use different migration modes during growth and metastasis—the spreading of cancer cells within the body.
Bo Sun, Oregon State University.
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3639: Cerebellum: the brain's locomotion control center
3639: Cerebellum: the brain's locomotion control center
The cerebellum of a mouse is shown here in cross-section. The cerebellum is the brain's locomotion control center. Every time you shoot a basketball, tie your shoe or chop an onion, your cerebellum fires into action. Found at the base of your brain, the cerebellum is a single layer of tissue with deep folds like an accordion. People with damage to this region of the brain often have difficulty with balance, coordination and fine motor skills. For a higher magnification, see image 3371.
This image was part of the Life: Magnified exhibit that ran from June 3, 2014, to January 21, 2015, at Dulles International Airport.
This image was part of the Life: Magnified exhibit that ran from June 3, 2014, to January 21, 2015, at Dulles International Airport.
Thomas Deerinck, National Center for Microscopy and Imaging Research, University of California, San Diego
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2781: Disease-resistant Arabidopsis leaf
2781: Disease-resistant Arabidopsis leaf
This is a magnified view of an Arabidopsis thaliana leaf a few days after being exposed to the pathogen Hyaloperonospora arabidopsidis. The plant from which this leaf was taken is genetically resistant to the pathogen. The spots in blue show areas of localized cell death where infection occurred, but it did not spread. Compare this response to that shown in Image 2782. Jeff Dangl has been funded by NIGMS to study the interactions between pathogens and hosts that allow or suppress infection.
Jeff Dangl, University of North Carolina, Chapel Hill
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2309: Cellular polarity
2309: Cellular polarity
As an egg cell develops, a process called polarization controls what parts ultimately become the embryo's head and tail. This picture shows an egg of the fruit fly Drosophila. Red and green mark two types of signaling proteins involved in polarization. Disrupting these signals can scramble the body plan of the embryo, leading to severe developmental disorders.
Wu-Min Deng, Florida State University
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3626: Bone cancer cell
3626: Bone cancer cell
This image shows an osteosarcoma cell with DNA in blue, energy factories (mitochondria) in yellow, and actin filaments—part of the cellular skeleton—in purple. One of the few cancers that originate in the bones, osteosarcoma is rare, with about a thousand new cases diagnosed each year in the United States.
This image was part of the Life: Magnified exhibit that ran from June 3, 2014, to January 21, 2015, at Dulles International Airport.
This image was part of the Life: Magnified exhibit that ran from June 3, 2014, to January 21, 2015, at Dulles International Airport.
Dylan Burnette and Jennifer Lippincott-Schwartz, NICHD
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3386: HIV Infected Cell
3386: HIV Infected Cell
The human immunodeficiency virus (HIV), shown here as tiny purple spheres, causes the disease known as AIDS (for acquired immunodeficiency syndrome). HIV can infect multiple cells in your body, including brain cells, but its main target is a cell in the immune system called the CD4 lymphocyte (also called a T-cell or CD4 cell).
Tom Deerinck, National Center for Microscopy and Imaging Research (NCMIR)
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2801: Trajectories of labeled cell receptors