GAO Xin, YANG Xian-Yu, ZHU Jia-Jun, YUAN Jin-Qiang, WANG Yi-Wen, SONG Min-Guo

(The Nurturing Station for the State Key Laboratory of Subtropical Silviculture, Zhejiang A & F University, Lin’an 311300, China)

New details indicated by different stainings during conjugation of ciliated protozoaParamecium

GAO Xin, YANG Xian-Yu*, ZHU Jia-Jun, YUAN Jin-Qiang, WANG Yi-Wen, SONG Min-Guo

(The Nurturing Station for the State Key Laboratory of Subtropical Silviculture, Zhejiang A & F University, Lin’an 311300, China)

During conjugation ofParameciumcaudatum, nuclear events occur in a scheduled program.Morphological studies on nuclear behavior during conjugation ofP.caudatumhave been performed since the end of the 19th century. Here we report on new details concerning the conjugation ofP.caudatumthrough the staining of conjugating cells with protargol, carbol fuchsin solution, Hoechst 33342 and immunofluorescence labeling with monoclonal antibody of anti-α tubulin. 1) The crescent nucleus is a characteristic of the meiotic prophase ofP.caudatum,has an unstained area. We stained this area with protargol, which was separated from the chromatin area and was not detected by the other stainings. 2) In regards to the four meiotic products, it has long been considered that only one product enters the paroral cone region (PC) and survives after meiosis. However, our protargol and immunofluorescence labeling results indicated that PC entrance of the meiotic product happened before the completion of meiosis instead of after. 3) In our previous study, protargol staining indicated the presence of a swollen structure around the central part of the “U” and “V” shaped spindles connecting the two types of prospective pronuclei. However, immunofluorescence labeling with anti-α tubulin antibodies gave a different image from protargol. All these observations form the basis for further studies of their molecular mechanisms.

Paramecium; Conjugation; Crescent; PC entrance; Connecting spindles

Morphological studies on nuclear behavior during conjugation ofParameciumcaudatumhave been studied since the end of the 19th century (Maupas, 1889; Calkins& Cull, 1907). In addition, many similar studies on otherParameciumand ciliates have been performed before and during the 1980s (Nanney, 1980; Wichterman, 1986).Over the last 30 years, much ciliate research has focused on mechanisms to interpret morphological phenomenaby molecular biological techniques, and some remarkable results have been obtained such as the discoveries of telomere, telomerase and ribozyme(Blackburn & Gall, 1978; Cech & Bass, 1986; Greider &Blackburn, 1985). However, fewer morphological studies have been done. Comparison of images obtained from the same cells by different stainings led to new findings in our previous study (Gao et al, 2010).Therefore, several staining methods were used to restudy the conjugation process ofP.caudatum, including the protargol technique (Shi, 1987), carbol fuchsin solution staining (Carr & Walker, 1961), Hoechst 33342(Santos et al, 2000) and immunofluorescence labeling with monoclonal antibody of anti-α tubulin (Yang &Takahashi, 2002). We discovered new details concerning conjugation ofP.caudatum, which are reported here.

1 Materials and Methods

1.1 Chemicals and preparation of staining solutions

Silver protein from Merck KGaA (Germany),monoclonal antibody of mouse anti-α tubulin, FITC-conjugated goat anti-mouse IgG, propidium iodide (PI)and Hoechst 33342 (HO) purchased from Beyotime Institute of Biotechnology (China) were used. All other chemicals were from Hangzhou Dafang Chemical Reagent Inc (China). Preparations of stock solutions for Hoechst 33342 and carbol fuchsin solution followed previous descriptions (Carr & Walker, 1961; Yang &Takahashi, 1999; Yang et al, 2007).

1.2 Cell culture, conjugation induction and stainings

Two complementary mating types ofP.caudatumcollected from East Lake Campus of Zhejiang A & F University (China) were used. Cell culture, conjugation induction, and collection of synchronized conjugating pairs followed previous studies (Dryl, 1959; Hiwatashi,1968; Sun et al, 2010; Wei et al, 2008; Yang &Takahashi, 1999). Modified protargol (Shi, 1987) briefly reported before (Shi & Frankel, 1990; Yang & Shi, 2007)was used. Immunofluorescence labeling with anti-α tubulin antibody followed Yang & Takahashi (2002).Temporary preparations were made by means of“volume-fixing” (Yang et al, 2008; Lin et al, 2009). All experiments were performed at room temperature (～25 °C).

2 Results and Discussion

2.1 A structure in crescent nuclei indicated by protargol technique

The crescent nucleus is a characteristic of the meiotic prophase ofP.caudatum, in which there is an unstained area (Fujishima & Hiwatashi, 1981; Harumoto& Miyake, 1996). To determine if protargol provides any new indications about this structure, conjugating pairs during the meiotic prophase were stained (Fig. 1C, C′, F,F′). In addition, cells at the same developmental stage were also stained by Hoechst 33342 (Fig. 1A, A′, D, D′)and carbol fuchsin solution (Fig. 1B, B′, E, E′). As in former reports, an unstained structure was observed in the crescent nuclei when cells were stained either by Hoechst 33342 or by carbol fuchsin solution (Fig. 1D, D′,E, E′). In contrast to this, a protargol stained structure separated from chromatin was observed (Fig. 1F, F′),which was exactly the area not detected by the other two stainings (compare Fig. 1D, E, F; D′, E′, F′). Before the crescent stage, micronuclei form a truncated spindle shape when cells were stained by Schiff reagent(Fujishima, 1983). Both Hoechst 33342 and carbol fuchsin solution staining in the current study also showed the micronuclei as truncated spindle shapes (Fig. 1A, B,A′, B′). However, protargol staining indicated that the micronucleus was a fully spindle shape consisting of two parts, thread-like chromatin and evenly stained nonchromatin (Fig. 1C, C′). The non-chromatin area was located at one end of the nucleus corresponding to the truncated area indicated by Hoechst 33342 and carbol fuchsin solution. The nature of this structure might be related with microtubule organizing center (MTOC). To date, immunofluorescence labeling with anti-gammatubulin antibodies indicated that during conjugation ofParamecium, only a transient site of gamma-tubulin and microtubule assembly was observed at the site of nuclear exchange (Klotz et al, 2003). To clarify the relationships among microtubules, gamma-tubulin and MTOCs,further research needs to be done with the help of molecular biological techniques.

2.2 Entrance of meiotic product into paroral cone region

Fig. 1 Micronuclei on meiotic prophase of Parameciumcaudatum

After meiosis, four meiotic products are produced,among which only one enters the paroral cone region(PC) (the area surrounding the disintegrated oral apparatus) and survives to complete the third prezygotic division producing a migratory and stationary pronucleus(Wichterman, 1986; Yanagi, 1987; Yanagi & Hiwatashi,1985), while the remaining three undergo apoptotic degeneration (Yang et al, 2007; Gao et al, 2010).Recently, immunofluorescence labeling with monoclonal antibodies of anti-α tubulin indicated that at least one of the meiotic products was located in the PC area at the telophase of the second meiotic division (Gao et al,2011b). To know the precise timing of PC entrance,many conjugating pairs were stained either by protargol technique or immunofluorescence labeling with anti-α tubulin antibodies. Both stainings indicated two cases of PC entrance (Fig. 2). One was during telophase of the second meiotic division (Fig. 2B, B′, G-I), when the meiotic nuclei showed a teardrop form. The other was soon after meiosis (Fig. 2D, D′, J), when all meiotic products showed spindle shapes without degenerating symptoms. Protargol staining indicated that PC entrance occurred in 70% of conjugants during the telophase of the second meiotic division, and in 96.3% soon after meiosis. In the case of immunofluorescence labeling, PC entrance was observed in 94.6% of conjugants during telophase of the second meiotic division, and 100% of conjugants after meiosis. However, PC entrance was observed neither at the telophase nor after the completion of the first meiotic division (Fig. 2E, F). These observations indicated that PC entrance of meiotic products was a specific phenomenon, which mainly happened during telophase of the second meiotic division instead of after meiosis. Based on electron microscopic analysis of transverse sections of jointedP.caudatumat the junction zone (André & Vivier, 1962; Vivier &André, 1961; Vivier, 1965), it has been suggested that a paroral cone is not present during the conjugation(Wichterman, 1986). In the current experiment, the paroral cone region was clearly observed (Fig. 2A-D),and might be involved in the protection of meiotic products from degeneration. We are not sure whether this observed difference was from different techniques or different syngens ofP.caudatum.

2.3 A protargol staining-indicated structure in the spindles connecting prospective migratory and stationary pronuclei

Fig. 2 PC entrance of meiotic products in Parameciumcaudatum

After meiosis, the haploid nucleus located in the PC region divides mitotically (the third prezygotic division)yielding two types of pronuclei (Wichterman, 1986).Recently, it has been indicated by both protargol staining and immunofluorescence labeling with anti-α tubulin antibodies that “U” and “V” shaped spindles connect prospective migratory and stationary pronuclei at the telophase of the third prezygotic division (Gao et al,2011a, b). For easier comparison, the same experiments were repeated in the current study. The “V”-shaped spindles and side-by-side localization of the two prospective pronuclei were observed (Fig. 3). Protargol staining indicated the presence of a swollen structure at the crossing points of the “V”-shaped spindles (circles in Fig. 3A-C, A′-C′), while immunofluorescence labeling with anti-α tubulin antibodies indicated a slender line structure at the same area. In other words, this protargolstained structure consisted of microtubules and some other unknown components. It is not clear if this structure corresponded to the structure in the crescent nuclei indicated in the current study, or functioned as MTOC. Besides these, there were two new points that have never been reported. The first was that the stationary pronuclei were much closer to the migratory pronuclei in Fig. 3C than in Fig. 3A and B. To clarify this, many conjugating pairs covering the third prezygotic division have to be stained and measured and statistically analyzed. The second is that many anti-α tubulin recognized dots were observed surrounding both types of prospective pronuclei. It has been previously reported that both intranuclear and cytoplasmic microtubules play important roles on pronuclear behavior (Nakajima et al, 2001). This current study indicated that both cytoplasmic and intranuclear microtubules appeared much earlier than the stage of pronuclear transfer.

Fig. 3 Telophase of the third prezygotic division of Parameciumcaudatum

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不同染色方法揭示纖毛原生動物草履蟲接合生殖過程的新細(xì)節(jié)

高 欣, 楊仙玉*, 朱嘉駿, 袁進強, 王逸雯, 宋敏國

（浙江農(nóng)林大學(xué) 亞熱帶森林培育國家重點實驗室培育基地，浙江 臨安 311300）

通過石炭酸品紅、Hoechst 33342、蛋白銀及免疫熒光標(biāo)記等染色方法對草履蟲接合生殖過程進行了重新觀察，結(jié)果發(fā)現(xiàn)：1）新月核是第一次減數(shù)分裂前期小核的主要形態(tài)學(xué)特征，在核內(nèi)有一未被石炭酸品紅、Hoechst 33342著色區(qū)域，蛋白銀染色則清楚顯示該結(jié)構(gòu)；2）4個單倍體減數(shù)分裂產(chǎn)物中的 1個核進入口旁錐完成配前第三次核分裂，其余3核退化。蛋白銀染色和抗α微管蛋白單克隆抗體進行免疫熒光標(biāo)記顯示，核進入口旁錐的時期在第二次減數(shù)分裂末期而非減數(shù)分裂結(jié)束后；3）配前第三次分裂末期，核間連絲的中間段有一被蛋白銀識別的結(jié)構(gòu)，但免疫熒光標(biāo)記卻無顯示, 只表現(xiàn)為纖維狀結(jié)構(gòu)與兩側(cè)核間連絲相連。觀察結(jié)果為草履蟲接合生殖過程中相關(guān)分子生物學(xué)機制研究奠定了必要的形態(tài)學(xué)基礎(chǔ)。

草履蟲；接合生殖；新月核；進入口旁錐；核間連絲

Q959.117.04；Q954.44

A

0254-5853-(2011)06-0651-06

2011-08-04；接受日期：2011-09-18

國家自然基金項目(30670397; 31071181); 教育部留學(xué)回國人員科研啟動基金項目([2007]1108); 浙江省教育廳一般項目(Y200804256); 浙江農(nóng)林大學(xué)科研發(fā)展基金項目(2292000030); 浙江省大學(xué)生科技創(chuàng)新活動計劃(新苗人才計劃)項目(2010R412003);浙江農(nóng)林大學(xué)大學(xué)生科技創(chuàng)新活動項目(100203,100224)

高欣，男，講師；研究方向：動物學(xué)；E-mail：wildlife909@yahoo.cn

10.3724/SP.J.1141.2011.06651

date: 2011-08-04; Accepted date: 2011-09-18

*Corresponding author (通訊作者), E-mail: xianyu_yang@hotmail.com