ConductVision Morphology

Glia, Quantified

Microglia ramification, astrocyte territory, oligodendrocyte process complexity — measured at cohort scale with batch reproducibility. Activation states classified per cell, longitudinal change tracked across timepoints.

3 cell types, 12+ markersPer-cell activation classCohort-scale batch processing
Iba1 / TMEM119GFAP / S100BMBP / Olig2
Microglia
Iba1 · CX3CR1 · TMEM119
Astrocytes
GFAP · S100B · ALDH1L1
Oligodendrocytes
MBP · Olig2 · CC1
Multi-Marker
Co-localised phenotyping

Four Metrics. Whole-brain Reach.

The morphology shifts before the transcriptome does. Quantify the change before you call it gliosis.

METRIC · 01

Ramification Index

Per-cell process complexity from Iba1+ skeletons — total branch length, end-point count, branch order, soma area. Discriminate ramified, hyper-ramified, and amoeboid microglia at scale.

RI = Σ branch_len / soma_area
METRIC · 02

Territory Volume

Astrocyte domain volume from 3D convex hull plus skeletal extent. Captures process span, primary process count, and neighbour-domain overlap — the readout that moves first under reactive gliosis.

V = ConvexHull(skeleton)
METRIC · 03

Activation Classification

Per-cell morphological state assignment — homeostatic, reactive, primed, hyper-ramified. Threshold-based or trained-classifier modes with QC overlays so you can see why each cell got its label.

class = f(RI, soma, sphericity)
METRIC · 04

Batch Comparison

Cohort-scale processing across full sections or atlas regions. Group-level statistics by treatment, genotype, brain area, and timepoint — without re-running ImageJ macros for each animal.

cohort × region × timepoint

Markers by Cell Type

Single-marker workflows or co-stained multi-channel — the same engine reads both. Phenotype across markers per cell.

Cell TypeCommon MarkersMorphometry Output
MicrogliaIba1CX3CR1-GFPTMEM119P2RY12Ramification index, branch count, end-point density, soma area, sphericity, activation class.
AstrocytesGFAPS100BALDH1L1AQP4Territory volume, process span, primary process count, neighbour overlap, reactive score.
OligodendrocytesMBPOlig2CC1 (APC)MAGProcess complexity, internode length, sheath count (with MBP), maturation stage.

Multi-marker co-staining supported across all three cell types.

Activation, Per Cell

Each cell carries its own morphology vector and class label, with QC overlays showing why. Longitudinal change tracked across timepoints in the same region.

Homeostatic
Ramified
Many fine processes, small soma, surveying the parenchyma. RI > 4.0, sphericity < 0.45.
Reactive
Bushy / Hyper-ramified
Thicker processes, larger soma, more terminal branching. RI 2.0–4.0, soma area > baseline.
Amoeboid
Phagocytic
Few short stubs, enlarged round soma, retracted processes. RI < 1.0, sphericity > 0.7.

From Z-Stack to Cohort Statistics

Four steps. One pipeline. No ImageJ macro per animal.

Acquire
Confocal Z-stacks, light-sheet volumes, OME-TIFF · single or multi-channel
Segment
Per-cell instance segmentation across markers · soma + process tree
Quantify
Ramification, territory, sheath count · activation class per cell
Compare
Cohort × region × timepoint statistics · publication-ready exports

Built on the Methods That Work

The morphometric definitions the field already trusts — codified, batched, reproducible.

GLIA
Quantitative analysis of cellular inflammation after traumatic spinal cord injury
Donnelly DJ, Popovich PG · 2008
Nature Neuroscience
Resting microglial cells are highly dynamic surveillants of brain parenchyma
Nimmerjahn A, Kirchhoff F, Helmchen F · 2005
J. Neuroscience Methods
Quantification of microglial morphology in murine brain by skeleton analysis
Young K, Morrison H · 2018
Frontiers in Neuroanatomy
Astrocyte territories are non-overlapping in adult mammalian cortex
Halassa MM, Fellin T, Takano H et al. · 2007

Glia, Quantified at Scale

Morphology shifts before transcripts do. Bring your Z-stacks; we will return per-cell metrics, activation classes, and cohort statistics ready for the next figure.