Ivan Radin

@radinbio.bsky.social

🌱🪴🌿🔬🏳️‍🌈 Lover of plants and microscopy. Assistant Professor, Department of Plant and Microbial Biology, Univerisity of Minnesota. Lab: radinlab.org/ Instagram: radinbio

The 5th Annual PCA Core Network Participant (CNP) Meeting took place this past weekend in St. Louis, MO! It was a great opportunity to celebrate accomplishments from the past year, connect with colleagues from across the network, and discuss the next phase of the PCA.

PCA Members are excited to share our new paper, which outlines a roadmap for tracing the origins & diversification of cell types across green plants using single-cell technologies. From algae to angiosperms, we're entering a new era of comparative cell biology. bit.ly/4eAip2Q

A single-cell blueprint for cellular diversity in the Green Lineage

The Green Lineage (Viridiplantae) represents one of the most successful evolutionary radiations on Earth, with remarkable morphological diversity from…

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These epidermal cells of tobacco (Nicotiana benthamiana) leaf are expressing cytosolic GFP. The brightest region is the nucleus, which is surrounded by a large central vacuole. The cytosol is restricted to the cell periphery. Transvacuolar strands connect the nucleus with other parts of the cell.

Fluorescence microscopy image showing glowing red cells with bright yellow centers and branching extensions against a black background; scale bar indicates 20 µm.

This is a section of juvenile moss (Physcomitrium patens) tissue, called protonemata. The apical cells expand by tip-growth, while subapical cells sometimes divide to make lateral filaments. Cytosolic GFP is in green, and chlorophyll autofluorescence is in magenta. #microscopymonday #moss

Fluorescence microscopy image showing a dense network of thin, branching filamentous structures, colored in green and magenta against a black background. The filaments overlap and extend in multiple directions. A scale bar in the lower right corner indicates 250 µm.

An undergraduate student in the lab, Andy Marchant, made this awesome image of a moss (Physcomitrium patens) apical chloronema cell. This is a beautiful example of how the ER network looks in plant cells (in green). The chlorophyll autofluorescence is in magenta. #microscopymonday #moss

Fluorescence microscopy image showing a green cellular ER network with magenta oval chloroplasts on a black background, with a 3 µm scale bar.

The Plant Science Art Exhibit is now on display at the University of Minnesota's College of Biological Sciences! This exhibit will be up for the rest of the semester to engage students and inform them about the history and potential of plant science! Learn more about the exhibit: bit.ly/4byqtQo

An art poster of George Washington Carver displayed in a university hallway.An art poster on Phytoremediation displayed in a university hallway.

We were testing lasers and the spectral ability of our confocal (FV3000) on a zoomed-in section of a Brassica rapa leaf. But when we zoomed out, we saw that the lasers we used photobleached chlorophyll autofluorescence in the square area we had zoomed in on. We used a 10x/0.4 objective for this.

Red fluorescence microscopy image showing a dense, mottled red signal across the field with a distinct dark, square-shaped region at the center where fluorescence is absent or reduced; a 100 µm scale bar appears in the lower-right corner.

These Brewer's yeast cells were in a hurry! This was captured with a point-scanning confocal microscope, which scans one point (pixel) at a time, moving from left to right and top to bottom. As a consequence, cells moving faster than the scan speed appear as streaks or exhibit distortions.

Image shows a gray-scale image of many circular-shaped yeast cells. There are also many streaks caused by fast-moving cells.

Today I made a small but momentous start to work in 2026 by changing a single number. I renamed the file “Papers to write and submit in 2025” to “Papers to write and submit in 2026”. Stay tuned for more file updates on 1st January 2027.