Membrane lipid raft organization during cotton fiber development

Abstract

Background

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 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.

Methods

The 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.

Results

We 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.

Conclusions

We 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.

Background

Cotton is the premier natural fiber for textiles. Cotton fibers are highly elongated single cells of the seed epidermis. The unicellular extremely elongated structure makes cotton fiber cell an ideal model for studying plant cell growth (Kim and Triplett 2001; Shi et al. 2006; Singh et al. 2009a; Qin and Zhu 2011). 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 rate reaches a peak in approximate 10 DPA, and the fibers finally grow to 30–40 mm length (Liu et al. 2012). Subsequently, the elongation of fiber cells completely stops, and the fibers enters a stable secondary wall deposition period (20–45 DPA) (Singh et al. 2009b), followed by a dehydration period (45–50 DPA), which generates mature fibers.

Extremely elongated fiber cells require change in cell turgor pressure, plasmodesmatal regulation, and transporter activities (Ruan et al. 2004; Zhu et al. 2003). A large-scale transcriptome analysis revealed that during fiber cell elongation, lipid metabolism pathways are up-regulated significantly (Gou et al. 2007). According to a cotton lipid spectrum analysis, the amount of unsaturated fatty acids in elongation stage fiber cells (α-linolenic acid: C18:3) is greater than that in ovules, and the amount of very-long-chain fatty acids (VLCFAs, from C20 to C26) eventually increases to three to five times (Wanjie et al. 2005). In addition, treating in vitro cultured cotton ovules with VLCFAs can promote the elongation of cotton fibers significantly, while treating with VLCFAs inhibitor acephrachlor (ACE) completely inhibits fiber growth, indicating that VLCFAs are involved in the cotton fiber elongation process (Qin et al. 2007). The study on Δ12 fatty acid desaturase revealed that the formation of unsaturated fatty acids under cold stress could maintain the specific membrane structure required for fiber elongation (Kargiotidou et al. 2008). Furthermore, plant-specific glycosylphosphatidylinositol (GPI) anchoring protein encoded gene COBL influences the orientation and crystallinity of fiber microfilaments, and is closely linked to fiber development (Roudier et al. 2010; Niu et al. 2019). During the rapid elongation stage, high phytosterol concentrations were also observed. In addition, numerous plant sterol biosynthesis genes were down-regulated in the short fiber of the Li-1 mutant, indicating that plant sterol also participates in the development of cotton fiber (Deng et al. 2016). VLCFAs are some of the substrates required for the synthesis of sphingolipids, and GPI is a precursor in the synthesis of complex sphingolipids. Sphingolipids and sterols are critical structural components of cell membranes, organelle membranes, and vacuolar membranes, and they form membrane lipid rafts (Hill et al. 2018). The relationship between the substances and fiber development indicates that the fiber membrane plays an important role in fiber development. However, the roles of membrane lipid raft in the development of cotton fiber remain unclear.

Fluorescent probes have been extensively used as biomarkers in biological studies. Laurdan and di-4-ANEPPDHQ are two phase-sensitive membrane probes and they respond uniquely to lipid packing, in a manner different from membrane associated peptides (Dinic et al. 2011). Laurdan and di-4-ANEPPDHQ display blue shifts of approximately 50 nm in their emission peaks for membranes in liquid-ordered (lo) phase relative to membranes in liquid-disordered (ld) phase (Jin et al. 2005; Jin et al. 2006), and can be quantified by calculating the generalized polarization (GP) values (Aron et al. 2017). Laurdan is a type of ultra violet-excited dye that is usually imaged using a two-photon excited fluorescence (TPF) microscope to avoid the photobleaching tendency observed under single-photon excitation (Jin et al. 2005). The peak emission spectrum of Laurdan has been reported to be at 440 nm for lo phase and 490 nm for ld phase (Dinic et al. 2011). Di-4-ANEPPDHQ is a single photon excited dye, and its spectrum range is in the 500–750 nm, covering the entire spectral range of most microscope systems (Owen and Gaus 2010), while the spectrum blue shift of the di-4-ANEPPDHQ dye is 60 nm (Aron et al. 2017). Quantitative in vivo imaging of lipid raft using di-4-ANEPPDHQ in artificial membrane systems and animal cells is well established (Owen et al. 2006; Owen and Gaus 2010; Owen et al. 2012). A few studies have mentioned the application of di-4-ANEPPDHQ in the visualization of plasma membrane microdomains in plant cells (Roche et al. 2008; Liu et al. 2009; Zhao et al. 2015).

Materials and methods

Plant materials

Wild-type Jimian 14 (Gossypium hirsutum L. cv. Jimian 14) was provided by professor MA Zhiying (Hebei Agricultural University) and was propagated and preserved at the Biotechnology Research Center of Southwest University. Short fiber cotton mutant Ligon lintless (Li-1) was provided by the Institute of Cotton Research, Chinese Academy of Agricultural Sciences, and the corresponding wild type (TM-1) for Li-1 mutant was segregated from a heterozygous Li-1 mutant. All plants were grown under natural conditions in the experimental field of the Biotechnology Research Center of Southwest University in Chongqing.

In vitro cotton ovule culture

Cotton ovules were collected 1 day after flower opening (defined as 1 DPA), soaked in 75% ethanol for 1 min, rinsed in distilled and deionized water, and soaked again in 0.1% (W/V) HgCl solution containing 0.05% Tween-80 at 100 g for 10 min to sterilize. Ovules were placed in Beasley and Ting’s medium under aseptic conditions (Beasley and Ting 1973).

Di-4-ANEPPDHQ staining

Di-4-ANEPPDHQ was purchased from Invitrogen (CAT #D36802). The stock solution of di-4-ANEPPDHQ [5 mmol·L^− 1 in dimethyl sulphoxide (DMSO)] was stored in dark at − 20 °C. For di-4-ANEPPDHQ staining, the in vitro cultured cotton ovules were incubated in staining solution as described in Results.

Confocal laser scanning microscope observation

An SP8 confocal laser scanning microscope (SP8 CLSM, Leica, Germany) was used for the imaging of di-4-ANEPPDHQ-labelled cotton fibers. The sample was excited using a 488-nm laser, and the emission spectra were 500–580 nm (green) and 620–720 nm (red). A 63× oil immersion objective (N.A. = 1.3) was used in this study. Identical microscope settings were maintained for quantitative imaging of membrane components.

GP processing

After CLSM imaging, generalized polarization (GP) images were generated by a previously described protocol (Owen et al. 2012), with some modifications. Briefly, the GP values were calculated according to the following equations:

$$ \mathrm{GP}=\left({\mathrm{I}}_{500-580}-\mathrm{G}\times {\mathrm{I}}_{620-720}\right)/\left({\mathrm{I}}_{500-580}+\mathrm{G}\times {\mathrm{I}}_{620-720}\right) $$

$$ \mathrm{G}=\left({\mathrm{GP}}_{\mathrm{ref}}+{\mathrm{GP}}_{\mathrm{ref}}{\mathrm{GP}}_{\mathrm{mes}}-{\mathrm{GP}}_{\mathrm{mes}}-1\right)/\left(\mathrm{GPmes}+{\mathrm{GP}}_{\mathrm{ref}}\mathrm{GPmes}-{\mathrm{GP}}_{\mathrm{ref}}-1\right) $$

I indicates the fluorescence intensity of each pixel of the image obtained within the receiving range of the two channels; G is the calibration constant; GP_mes is the calibrated GP value of di-4-ANEPPDHQ in pure DMSO solution with similar device parameters; when the ordered phase and the disordered phase are separated, GP_ref = 0. The fluorescence intensity value of each image was calculated using Image J 1.46 (https://imagej.nih.gov/ij/download.html).

Ratio image processing

Dual-channel ratio imaging (ratio) can be used for quantitative analysis of membrane organization (Jin et al. 2005). In the present study, fluoviewFV1000 was used for ratio imaging of di-4-ANEPPDHQ stained cotton fiber cells. The formula for calculating ratio images is as follows:

$$ {\mathrm{Ratio}}_{\mathrm{r}/\mathrm{g}}=\left({\operatorname{int}}_{\mathrm{r}}-{\mathrm{bkg}}_{\mathrm{r}}\right)/\left({\operatorname{int}}_{\mathrm{g}}-{\mathrm{bkg}}_{\mathrm{g}}\right)\times \mathrm{MF} $$

int_r and int_g represent the fluorescence intensities of red channel and green channel images, respectively; bkg_r and bkg_g represent the background values set for int_r and int_g, respectively; the background values are set similarly to avoid interference. MF is the multiplication factor.

Results

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. Considering di-4-ANEPPDHQ is used as probe for detecting membrane order. In the present study, we use the fluorescent dye to detect the membrane lipid raft organization in cotton fiber cells. First, we investigated the toxicity of di-4-ANEPPDHQ to cotton fiber growth and development. Following exogenous application of di-4-ANEPPDHQ at various concentrations, we observed that the lengths of di-4-ANEPPDHQ-treated cotton fibers were similar to those of untreated fibers after culture for similar periods (Fig. 1). The results indicated that di-4-ANEPPDHQ is a low toxicity fluorescent probe for cotton fiber and could be used for the observing of lipid raft microregions of cotton fiber cells.

Fig. 1

Effects of di-4-ANEPPDHQ on the growth of cotton fiber cells. Cotton ovules were treated with 0 μmol·L^− 1, 2 μmol·L^− 1, 4 μmol·L^− 1, 6 μmol·L^− 1 di-4-ANEPPDHQ and cultured in vitro for 5 day, 10 day and 15 day

The fluorescence emission spectra of di-4-ANEPPDHQ in cotton fibers

Di-4-ANEPPDHQ is a fluorescent probe that responds rapidly to changes in electric potential in the environment. Its spectral characteristics are related to environment, cell type, and electric potential. To determine the spectral characteristics of di-4-ANEPPDHQ in fiber cells, we used excitation light at 488 nm to collect emission spectra at 10-nm intervals in a lambda acquisition mode and calculated the spectral intensity. The range of emission fluorescence intensity of di-4-ANEPPDHQ-dyed cotton fiber cells was 550–660 nm and the peak emission fluorescence intensity was observed at 580 nm (Fig. 2).

Fig. 2

Spectral characteristics of Di-4-ANEPPDHQ in cotton fiber cells. a Raw images series taken by the lambda mode of confocal laser scanning microscope (CLSM) in WT cotton fiber cell stained with di-4-ANEPPDHQ. b Raw emission profile of di-4-ANEPPDHQ in wild type cotton fiber cell

The optimum labeling conditions of di-4-ANEPPDHQ for cotton fibers

Considering di-4-ANEPPDHQ is a very sensitive fluorescent probe, treatment time and concentrations are two key factors to be taken into account in the application of the dye. To determine the optimal labeling conditions for di-4-ANEPPDHQ for dyeing cotton fibers, we examined the fluorescence of di-4-ANEPPDHQ-stained fiber cells under different concentrations and treatment times. When the staining time was 3 min, the fluorescence signal could hardly be detected under the low concentration treatments (Fig. 3a), while treatment for 5 min with 3 μmol·L^− 1 di-4-ANEPPDHQ, yielded fluorescence images could be recorded (Fig. 3b). Therefore, we selected 3 μmol·L^− 1 and 5 min treatment as the optimal labeling conditions for staining cotton fiber cells using di-4-ANEPPDHQ.

Fig. 3

Optimized the di-4-ANEPPDHQ staining parameter for cotton fiber cells. a Di-4-ANEPPDHQ dye treatment for 3 min. b Di-4-ANEPPDHQ dye treatment for 5 min. 1 μmol·L^− 1, 2 μmol·L^− 1, 3 μmol·L^− 1, 4 μmol·L^− 1, 5 μmol·L^− 1, and 6 μmol·L^− 1 indicate the treatment concentrations

Membrane lipid raft order of wild-type cotton fibers

To understand the change regularity in plasma membrane lipid raft organization in the course of the development of cotton fiber cells, we detected the fluorescence signals at 0 DPA, 5 DPA, 10 DPA, 20 DPA, and 30 DPA, in fiber cells stained with di-4-ANEPPDHQ. The fluorescence intensity of the green channel (liquid-ordered phase, 500–580 nm) was stronger at 0 DPA, 5 DPA, and 10 DPA fibers, but weaker at 20 DPA and 30 DPA. Conversely, the fluorescence intensity of the red channel (liquid-disordered phase, 620–720 nm) was weaker in 0 DPA, 5 DPA, and 10 DPA fibers, but stronger in 20 DPA and 30 DPA fibers (Fig. 4). The results indicated that the plasma membrane order was higher at the early stages of fiber development, while the plasma membrane is disorder at the later stages of fiber development. Furthermore, the ratio (red/green) of the double channel fluorescence intensity was plotted, and the white color indicated that the membrane order and the lipid raft activity were low, while the blue color represented higher membrane order and lipid raft activity. The ratio images indicated that the fiber membranes at 0 DPA were almost all white and red; the blue were the highest at 10 DPA, with almost no distribution of white dot; the fiber membranes had a certain amount of white distribution at 20 DPA; the fiber membranes were almost all white at 30 DPA (Fig. 4). These suggested that at the initiation stage, the lipid order of fiber cell membrane and the lipid raft activity were lower, and the fiber cell membrane lipid order and lipid raft activity increased gradually as the fibers transitioned into the rapid elongation stage. In addition, with the termination of fiber cell elongation, fiber cells entered the secondary wall synthesis phase, and fiber cell membrane lipid order and lipid raft activity decreased. Therefore, during cotton fiber cell development, membrane lipid order and lipid raft activity change from low to high, then to low, and the physiological and biochemical activities of fiber cells were the greatest in elongation phase.

Fig. 4

Fluorescence imaging of di-4-ANEPPDHQ labeled wild-type cotton fiber cells. 500–580 nm, the green channel; 620–720 nm, the red channel; Merged, the merged channel of green and red channels; Ratio, the ratio images of red channel/ green channel. 0 DPA, 5 DPA, 10 DPA, 20 DPA, 30 DPA represent the period of cotton fiber cell development

For quantitative analysis of the obtained pictures, we calculated the generalized polarization (GP) values and red/green ratio (Ratio_r/g) values based on more images. The GP values in fiber cells at 0 DPA were relatively lower. With the development of fiber cells, the GP values increased gradually, reaching the peak at 10 DPA, and then decreased to the lowest level at 30 DPA (Fig. 5a). The results are consistent with the fluorescence signal observations, which also indicated that the fiber cell membrane lipid order and lipid raft activity were higher at the rapid elongation stage, and lower in the secondary wall synthesis phase. The Ratio_r/g value in the 10 DPA fiber cells was 0.557 ± 0.131, which was the lowest value observed in the course of fiber development. Conversely, the value was 1.410 ± 0.090 at 30 DPA, which was the highest value observed in the course of fiber development (Fig. 5a). The results suggest that the lipid raft activity, cell membrane order, and physiological activity of fiber cells were the greatest during the rapid elongation phase.

Fig. 5

The GP and Ratio value of wild-type cotton fiber. a The GP value of 0 DPA, 5 DPA, 10 DPA, 20 DPA, and 30 DPA wild-type cotton fibers. b The Ratio_r/g value statistics of 0 DPA, 5 DPA, 10 DPA, 20 DPA, 30 DPA wild-type cotton fibers

Membrane lipid raft order of Li-1 mutant cotton fibers

To further verify the relationship between lipid raft activity and fiber cell elongation development, we examined changes in GP value during the elongation of fiber cells of a short fiber mutant, Ligon lintless-1 (Li-1). Notably, the GP value in Li-1 mutant fibers was remarkably lower than the GP values in wild-type fibers at the similar development stages (Fig. 6), indicating that lipid raft activity was lower in mutant fiber cells. In addition, the GP value in wild-type fibers increased from 5 DPA to 10 DPA, while the GP value in mutant fibers decreased from 5 DPA to 10 DPA (Fig. 6), which further indicated that membrane lipid order and lipid raft activity were closely correlated with cotton fiber development.

Fig. 6

Fluorescence images and the GP value of Li-1 mutant fibers. a Confocal laser scanning microscope images of di-4-ANEPPDHQ stained 5 DPA (top) and 10 DPA (bottom) Li-1 fibers. 500–580 nm, the green channel; 620–720 nm, the red channel; Merged, the merged channel of green and red channels; Ratio, the ratio images of red channel/ green channel. b The GP value of 5 DPA and 10 DPA wild-type and Li-1 fibers

Discussion

Biomembranes play an important role in cell growth and development. The cotton fiber cell is one of the longest cells in plants. Owing to its highly elongated structure and high cellulose content, the cotton fiber serves as an excellent system for studying cell elongation, cell wall formation, and other fundamental aspects of plant cell growth and development (Kim and Triplett 2001).Therefore, it is assumed that membrane also play an important role in fiber growth. On the one hand, with the expansion of cell size, the area of the plasma membrane and the inner membrane needs to increase correspondingly; conversely, it serves as the site of attachment of most enzymes (about 80% of the enzymes are membrane-binding proteins, for example, the cellulose synthase complex is located in the plasma membrane). However, studying membrane functions and properties is challenging due to its dynamic structure and limited technologies. In recent years, following advancements in technologies, researchers have demonstrated that lipid rafts (lipid microdomains) are the functional domains of membranes using diverse approaches (Mongrand et al. 2004; Borner et al. 2005).

Plasma membranes (PMs) are composed of three major classes of lipids, including glycerolipids, sphingolipids, and sterols, which may account for up to 100 000 distinct molecular species (Yetukuri et al. 2008; Shevchenko and Simons 2010). Overall, all glycerolipids share similar molecular moieties in plants, animals, and fungi. In contrast, sterols and sphingolipids are varied and specific to each kingdom, and are the major components of lipid rafts (Cacas et al. 2016). Membrane lipid raft activity has become a major index for characterizing membrane properties. Higher order cell membranes and higher lipid raft activity could offer stable reaction platforms and ordered dynamic environment for various physiological and biochemical reactions (Maccioni et al. 2002; Yu et al. 2004), which are closely linked to the polar elongation of cells (Meder et al. 2006; Sorek et al. 2007; Cánovas and Pérez-Martín 2009). Over the last two decades, considerable progress has been made in cotton fiber studies. The components of lipid raft have been verified to play a key role in fiber development. For example, VLCFAs are required for fiber development and mainly served as precursors of sphingolipid biosynthesis (Qin et al. 2007). In addition, the compositions and concentrations of plant sterols influence fiber growth (Deng et al. 2016; Niu et al. 2019). Furthermore, it has been demonstrated that inhibiting sphingolipid synthesis seriously suppresses fiber cell growth. The results indicate that lipid rafts play a key role in the development of fiber cells. Therefore, it is critical to examine membrane lipid raft activity during fiber development.

The fluorescence probe di-4-ANEPPDHQ could bind both liquid-order (lo) and liquid-disorder (ld) phase membranes. Due to its strong polarity-dependent spectral shifts, di-4-ANEPPDHQ could stain lo and ld phase membranes in different colors (Klymchenko and Kreder 2014). Through fluorescence lifetime imaging and CLSM, the optical properties of di-4-ANEPPDHQ in animal cells have been well studied and applied to detect lipid raft activity in living cells (Owen et al. 2006, 2012). However, few studies that focus on plant cells have been performed. Roche et al. (2008) used the dye to explore changes in membrane lipid activity in BY2 cells following treatment with plant sterol chelate-β-cyclodextrin, and they demonstrated that the sterol influenced lipid raft activity significantly in plant cells. Liu et al. (2009) used di-4-ANEPPDHQ to investigate the aggregation of lipid micro area (lipid raft) at the tip of a pollen tube in Picea meyeri, which is analogous to the polar elongation of the pollen tube. In addition, Zhao et al. (2015) studied root epidermal cell and root hair cell using di-4-ANEPPDHQ in Arabidopsis, and reported that the ordered degree of plasma membrane was higher than that of the inner membrane in root epidermal and root hair cells.

In the present study, we investigated the toxicity and optical properties of di-4-ANEPPDHQ to cotton fiber cell. The toxicity of the di-4-ANEPPDHQ to fiber cell was relatively low. Furthermore, there was no obvious difference in fiber cell elongation between the fiber treated with 6 μmol·L^− 1 di-4-ANEPPDHQ and the control, which is similar to the results observed in root hair cells (Zhao et al. 2015). In the fiber cell, incubation with 3 mmol·L^− 1 of the di-4-ANEPPDHQ probe in the culture medium for 5 min at room temperature was adequate, while for root epidermal cells and root hairs, incubation with 5 mmol·L^− 1 of the di-4-ANEPPDHQ probe in the culture medium for 5 min at room temperature was adequate (Zhao et al. 2015). The results suggested that the optimal stain condition depended on the materials.

Changes in lipid raft activity in the plasma membrane were observed in the course of fiber cell development. In addition, the rapid elongation phase of the fiber cell exhibited higher lipid raft activity, while the elongation termination and the early elongation stages exhibited relatively low lipid raft activity, which showed that lipid raft activity of the plasma membrane and plasma membrane organization were closely related to fiber cell elongation. Phytosterol is one of components of lipid raft. During fiber growth, higher concentrations of sitosterol and campesterol, two major phytosterols, were detected in the rapid elongation phase fiber cells, when compared with the concentrations in the early fiber elongation and secondary cell wall deposition stages (Deng et al. 2016). The change in trends of membrane lipid raft activity was consistent with the phytosterol concentration trends oberserved in the course of fiber cell development. Roche et al. (2008) used cyclic oligosaccharide methyl-β-cyclodextrin, commonly used in animal cells to decrease cholesterol levels, to induce a drastic reduction (50%) in the total free sterol concentrations in PM of BY2 cells and the depletion of sterol concentrations increased lipid acyl chain disorder. The results confirm that higher phytosterol concentrations are associated with higher membrane lipid raft activity (membrane order). Since phytosterols and sphingolipids are two key components of lipid raft, further studies should focus on the role of sphingolipids and various molecule species of phytosterols or sphingolipids on lipid raft activity in the cotton fiber cell.

Conclusion

In the present study, we investigated lipid raft activity in cotton fiber cell during its developmental process by labeling it with di-4-ANEPPDHQ. Using an in vitro cotton ovule culture system, we verified that the dye exhibited low toxicity to cotton fiber, and we established the optimal labeling conditions of the dye for the cotton fiber plasma membrane as follows: incubation with 3 μmol·L^− 1 of the di-4-ANEPPDHQ probe for 5 min at room temperature. Based on the phase separation characteristics of di-4-ANEPPDHQ, dual channel images were obtained using CLSM (Leica SP8) and were processed based on GP values and a Ratio_r/g processing algorithm. According to the results, the membrane order degrees of cotton fiber cell exhibited a low-high-low change regularity with the development of cotton fiber cell. In addition, the regularity was disrupted in the short lint fiber Li-1 mutant. Overall, the results imply that there is a close relationship between cotton fiber cell development and cell membrane lipid organization and lipid raft activity.