# Soft X-ray spectromicroscopy of human fibroblasts with impaired sialin function

## TL;DR

This study uses soft X-ray spectromicroscopy to compare normal and Salla disease fibroblasts, revealing differences in macromolecular composition and the impact of a treatment compound.

## Contribution

The study introduces a novel application of STXM to analyze lysosomal storage disease cells and their response to treatment.

## Key findings

- SD fibroblasts showed lower relative protein concentration compared to normal fibroblasts.
- ManNAc treatment increased protein concentration in both SD and normal fibroblasts.
- Grid-grown cells provided clearer STXM spectra but limited analysis to thin cell regions.

## Abstract

Salla disease (SD) is a lysosomal storage disease where free sialic acid (SA) accumulates in lysosomes due to the impaired function of a membrane protein, sialin. Synchrotron radiation-based scanning transmission soft X-ray spectromicroscopy (STXM) was used to analyze both SD patients' fibroblasts and normal human dermal fibroblasts (NHDF) from healthy controls. Both cell lines were also cultured with N-acetyl-d-mannosamine monohydrate (ManNAc) to see if it increased SA concentration in the cells. The STXM technique was chosen to simultaneously observe the morphological and chemical changes in cells. It was observed that free SA did not remain in the lysosomes during the sample processing, leaving empty vacuoles to the fibroblasts. The total cytosol and entire cell spectra, however, showed systematic differences between the SD and NHDF samples, indicating changes in the relative macromolecular concentrations of the cells. The NHDF cell lines contained a higher relative protein concentration compared to the SD cell lines, and the addition of ManNAc increased the relative protein concentration in both cell lines. In this study, two sample preparation methods were compared, resin-embedded thin sections and cells grown directly on sample analysis grids. While the samples grown on the grids exhibited clean, well-resolved spectra not masked by embedding resin, the low penetration depth of soft X-rays hindered the analysis to only the thin region of the microfilaments away from the thick nucleus.

A comparative study of normal human fibroblasts and Salla disease patients' fibroblasts reveals changes in the soft X-ray spectroscopic signatures of disease cells. Synchrotron radiation imaging was performed for thin sections and grid-grown cells.