The organisation of hemicelluloses within the pollen intine of many monocots remains inadequately characterised, partly due to the masking of epitopes within complex wall matrices. In this study, mature pollen grains of Gagea lutea (L.) Ker-Gawl. were analysed using immunofluorescence and immunogold technique with a variety of monoclonal antibodies that target xyloglucan (LM15, LM24, LM25, CCRC-M48), heteroxylan (LM10, LM11), heteromannan (LM21, LM22), and xylan (CCRC-M138). Semithin sections of LR White were examined both untreated and following a sequential enzymatic pretreatment, which included alkaline de-esterification followed by treatment with pectate lyase (RbPel1A) and endo-β-mannanase 5A. In untreated pollen, xyloglucan-related epitopes were identified within the intine, accompanied by additional intracellular labelling for LM15, and LM25; while for LM24 signal was only to the intine ring. Conversely, CCRC-M48 exhibited a more punctate distribution. Neither xylan- nor mannan-related epitopes were detected in the wall or intracellularly. The enzymatic digestion significantly altered the detectability of epitopes, resulting in an increase in continuous wall labelling within the intine across multiple probes. These findings indicate that enzymatic modification of pectic and mannan components has a considerable impact on the apparent distribution of hemicellulose epitopes within the pollen wall of G. lutea. Together, these results expand the still limited in situ immunolocalisation evidence base for hemicellulose-related epitopes in pollen, and provide a practical framework for interpreting digestion-dependent changes primarily in terms of epitope accessibility within the intine matrix.
Kapusta et al. (2026) studied this question.