# Quantitative and Comparative Assessment of Recombinant Human β-Glucocerebrosidase Uptake Bioactivity Using a Stable hMMR-Expressing CHO Cell Model

**Authors:** Lyuyin Wang, Kaixin Xu, Ping Lyu, Xinyue Hu, Jing Li

PMC · DOI: 10.3390/molecules31020235 · 2026-01-10

## TL;DR

Researchers developed a new method to accurately measure how well different forms of a treatment for Gaucher disease are taken up by cells.

## Contribution

A novel bioassay using hMMR-expressing CHO cells was developed to reliably assess rhGCase uptake bioactivity.

## Key findings

- The new bioassay generates consistent sigmoidal dose–response curves for rhGCase uptake.
- Imiglucerase showed higher uptake activity than velaglucerase alfa in the assay.
- Uptake is specifically mediated by hMMR and involves transport to endosomes/lysosomes.

## Abstract

Inconsistent conclusions on the cellular uptake of recombinant human β-glucocerebrosidase (rhGCase) for Gaucher disease stem from a fundamental limitation of existing methods: their inability to generate complete and reliable dose–response curves. This critical flaw, stemming from susceptibility to various experimental variables, prevents accurate potency comparison across different rhGCase products. To address this, we developed a robust bioassay using CHO-K1 cells stably expressing the human macrophage mannose receptor (hMMR). Our method quantifies uptake by measuring the enzymatic activity of internalized rhGCase and consistently produces a classic sigmoidal dose–response curve. Comprehensive validation and mechanistic studies, including inhibition experiments with mannose, fucose, and mannose-6-phosphate, confirmed that uptake is specifically mediated by hMMR, with successful enzyme transport to endosomes/lysosomes. Applying this assay to three commercial products yielded results contrary to prior literature: imiglucerase demonstrated superior uptake activity to velaglucerase alfa. The proposed method represents a significant improvement over existing assays, providing a more accurate and reproducible means to evaluate cellular uptake bioactivity, which is crucial for the quality control of rhGCase therapeutics.

## Linked entities

- **Genes:** HMMR (hyaluronan mediated motility receptor) [NCBI Gene 3161]
- **Chemicals:** mannose (PubChem CID 18950), fucose (PubChem CID 17106), mannose-6-phosphate (PubChem CID 6101690)
- **Diseases:** Gaucher disease (MONDO:0018150)

## Full-text entities

- **Genes:** HMMR (hyaluronan mediated motility receptor) [NCBI Gene 3161] {aka CD168, IHABP, RHAMM}, GBA1 (glucosylceramidase beta 1) [NCBI Gene 2629] {aka GBA, GCB, GLUC}
- **Diseases:** Gaucher disease (MESH:D005776)
- **Chemicals:** velaglucerase alfa (-), mannose-6-phosphate (MESH:C027693), mannose (MESH:D008358), fucose (MESH:D005643)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12844381/full.md

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Source: https://tomesphere.com/paper/PMC12844381