Abstract

BackgroundCotton fiber is a single-celled seed trichome that originates from the ovule epidermis. It is an excellent model for studying cell elongation. Along with the elongation of cotton fiber cell, the plasma membrane is also extremely expanded. Despite progress in understanding cotton fiber cell elongation, knowledge regarding the relationship of plasma membrane in cotton fiber cell development remains elusive.MethodsThe plasma membrane of cotton fiber cells was marked with a low toxic fluorescent dye, di-4-ANEPPDHQ, at different stages of development. Fluorescence images were obtained using a confocal laser scanning microscopy. Subsequently, we investigated the relationship between lipid raft activity and cotton fiber development by calculating generalized polarization (GP values) and dual-channel ratio imaging.ResultsWe demonstrated that the optimum dyeing conditions were treatment with 3 μmol·L− 1 di-4-ANEPPDHQ for 5 min at room temperature, and the optimal fluorescence images were obtained with 488 nm excitation and 500–580 nm and 620–720 nm dual channel emission. First, we examined lipid raft organization in the course of fiber development. The GP values were high in the fiber elongation stage (5–10 DPA, days past anthesis) and relatively low in the initial (0 DPA), secondary cell wall synthesis (20 DPA), and stable synthesis (30 DPA) stages. The GP value peaked in the 10 DPA fiber, and the value in 30 DPA fiber was the lowest. Furthermore, we examined the differences in lipid raft activity in fiber cells between the short fiber cotton mutant, Li-1, and its wild-type. The GP values of the Li-1 mutant fiber were lower than those of the wild type fiber at the elongation stage, and the GP values of 10 DPA fibers were lower than those of 5 DPA fibers in the Li-1 mutant.ConclusionsWe established a system for examining membrane lipid raft activity in cotton fiber cells. We verified that lipid raft activity exhibited a low-high-low change regularity during the development of cotton fiber cell, and the pattern was disrupted in the short lint fiber Li-1 mutant, suggesting that membrane lipid order and lipid raft activity are closely linked to fiber cell development.

Highlights

  • Cotton fiber is a single-celled seed trichome that originates from the ovule epidermis

  • Di-4-ANEPPDHQ is a low toxicity fluorescent probe dye for cotton fibers During the growth and development of cotton fiber cells, the changes in cell morphology are closely related to the cell membrane

  • We investigated the toxicity of di-4-ANEPPDHQ to cotton fiber growth and development

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Summary

Introduction

Cotton fiber is a single-celled seed trichome that originates from the ovule epidermis. It is an excellent model for studying cell elongation. Along with the elongation of cotton fiber cell, the plasma membrane is extremely expanded. Cotton fibers are highly elongated single cells of the seed epidermis. The developmental process of cotton fiber consists of five distinctive but overlapping stages: initiation, elongation, transition, secondary cell wall deposition, and maturation (Haigler et al 2012). Lint fiber initiates elongation near the day of anthesis and continues up to approximately 21 days post anthesis (DPA). During this period, the elongation rate exhibits a slow-fast-slow regularity. The elongation of fiber cells completely stops, and the fibers enters a stable (2020) 3:13 secondary wall deposition period (20–45 DPA) (Singh et al 2009b), followed by a dehydration period (45–50 DPA), which generates mature fibers

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