Abstract

The algae Micrasterias with its star-shaped cell pattern is a perfect unicellular model system to study morphogenesis. How the indentations are formed in the primary cell wall at exactly defined areas puzzled scientists for decades, and they searched for chemical differences in the primary wall of the extending tips compared to the resting indents. We now tackled the question by Raman imaging and scanned in situ Micrasterias cells at different stages of development. Thousands of Raman spectra were acquired from the mother cell and the developing semicell to calculate chemical images based on an algorithm finding the most different Raman spectra. Each of those spectra had characteristic Raman bands, which were assigned to molecular vibrations of BaSO4, proteins, lipids, starch, and plant cell wall carbohydrates. Visualizing the cell wall carbohydrates revealed a cell wall thickening at the indentations of the primary cell wall of the growing semicell and uniplanar orientation of the cellulose microfibrils to the cell surface in the secondary cell wall. Crystalline cellulose dominated in the secondary cell wall spectra, while in the primary cell wall spectra, also xyloglucan and pectin were reflected. Spectral differences between the indent and tip region of the primary cell wall were scarce, but a spectral mixing approach pointed to more cellulose fibrils deposited in the indent region. Therefore, we suggest that cell wall thickening together with a denser network of cellulose microfibrils stiffens the cell wall at the indent and induces different cell wall extensibility to shape the lobes.

Highlights

  • The question of how a plant cell achieves its shape is central for basic cell biological research, and applied sciences, as morphogenesis of a single cell determines the shape of tissues and organs

  • Raman imaging on Micrasterias cells delivered a molecular fingerprint at every pixel

  • Starch, proteins, lipids, and barite were differentiated based on characteristic Raman spectra and their distribution followed within the mother cell and the growing semicell at two developmental stages (Figs. 1 and 3)

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Summary

Introduction

The question of how a plant cell achieves its shape is central for basic cell biological research, and applied sciences, as morphogenesis of a single cell determines the shape of tissues and organs. While at the beginning of morphogenesis the young semicells represent undifferentiated flat bulbs, first indentations are formed about 75 min after mitosis by a sudden stop of growth in two exactly defined, symmetrically arranged areas at the primary cell wall (Meindl 1993). This leads to the formation of the first indentations that become the deepest ones at the final cell shape. A rigid cellulose-rich secondary wall is deposited as soon as morphogenesis is completed and the primary wall is pushed off by a sudden onset of mucilage excretion through the cell wall pores (Lütz-Meindl 2016)

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