72 resultados para maturation


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As one of the most powerful tools in biomedical research, DNA sequencing not only has been improving its productivity in an exponential growth rate but also been evolving into a new layout of technological territories toward engineering and physical disciplines over the past three decades. In this technical review, we look into technical characteristics of the next-gen sequencers and provide prospective insights into their future development and applications. We envisage that some of the emerging platforms are capable of supporting the $1000 genome and $100 genome goals if given a few years for technical maturation. We also suggest that scientists from China should play an active role in this campaign that will have profound impact on both scientific research and societal healthcare systems.

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树突状细胞(dendritic cells, DC)作为机体天然免疫和获得性免疫反应的桥梁和枢纽,发挥着重要的启动和调控作用。随着体外诱导方法的建立和生物学技术的进步,有关DC 的基础生物学研究得到了快速的发展,在诱导方法、个体发生及基因表达和调控等方面,涌现出很多新的、未解的关键问题。同时,随着对粘膜免疫机理研究的深入,DC 在粘膜生态环境中的功能和影响,渐已成为免疫学研究前沿领域中的热点和要点。在本研究中,为了确定DC 体外分化成熟的最短时程,同时为了研究DC 分化成熟相关的基因表达调控,我们建立了快速的DC 体外诱导方法,分析了体外快速诱导 DC 的mi/mRNA 表达谱。此外,在原始分离的女性生殖道共生乳酸杆菌的基础上,以THP-1作为DC 前体细胞的细胞系模型,开展了女性生殖道共生乳酸杆菌刺激活化 THP-1 的研究,希望能够为乳酸杆菌作为生殖道粘膜免疫疫苗的应用提供理论基础。首先,采用外周血单个核细胞(peripheral blood mononuclear cells, PBMC)来源的CD14+细胞为DC 前体,经过GM-CSF 和IL-4 的刺激,1-6 天后得到未成熟DC (immature dendritic cells, iDC),并经成熟因子(TNF-α, IL-1β, IL-6 与PGE2)诱导 1-2 天后,获得成熟DC(mature dendritic cells, mDC)。经过比较和分析,明确了完全分化和成熟各2 天,即“2+2”,为DC 诱导分化的最佳和最短时程,从而证实和建立了DC 体外快速诱导的体系和方法。该方法获得的iDC 与mDC,具有与传统的“6+2” 方法获得的DC 相同的形态与表型,而且,利用该方法获得的DC 总数高于“1+1”, “1+2”与“6+2”的方法,为DC 的生物学研究提供了基础数据。我们进而采用芯片技术,对体外快速分化成熟的DC 进行了mi/mRNA 表达谱分析,确定了DC 不同分化发育阶段特征性的mi/mRNA 表达差异。结果发现,与CD14+ 单核细胞即DC 前体相比,iDC 与mDC 之间具有更加相近的mi/mRNA 表达方式。 miRNA 表达谱分析则表明,不同的miRNA 表达与DC 的不同分化和发育阶段相关。而且,位于同一基因簇内的miRNA,呈现协同表达的情况。特别值得注意的是,本研究发现了在DC 的某些发育阶段特异表达的miRNA,它们在DC 发育过程中的功能,还未得到诠释,它们在DC 某些分化阶段的特异表达,提示了DC 各分化阶段的相关性与特异性。结合mRNA 表达谱分析,我们发现miRNA 的表达与其目的基因的表达在mRNA 水平呈现负相关的特性。同时,免疫相关mRNA 与miRNA 在DC 体外不同发育阶段的表达亦呈现差异,其中,miRNA(如hsa-miR-181a, hsa-miR-223, hsa-miR-155, hsa-miR-146, hsa-miR-106a 与hsa-miR-20a 等)与mRNA(如ALM1 等)参与了特定的与免疫相关的GO(Gene Ontology)与通路(Pathway),提示这些miRNA 与mRNA 可能通过不同的方式调节控制着DC 的体外诱导过程。在有关粘膜生态环境中DC 的分化、成熟及其功能影响的研究中,我们首先通过各种乳酸杆菌鉴定方法的综合应用,确定了6 种原始分离的女性生殖道主要共生乳酸杆菌:发酵乳酸杆菌(L.Fermentum)、约氏乳酸杆菌(L.Johnsonni)、卷曲乳酸杆菌(L.Crispatus)、革氏乳酸杆菌(L.Gasseri)、詹氏乳酸杆菌(L.Jensenii)与德氏乳酸杆菌(L.Delbrueckii )。其中,德氏乳酸杆菌(L.Delbrueckii)和发酵乳酸杆菌(L.Fermentum)具有较高的产H2O2 的能力。在此基础上,我们在与THP-1 的共同培养体系中,将乳酸杆菌对DC 前体的作用和影响进行了比较和研究。结果发现,L.Crispatus 在分离的各原始菌株中,具有最强的刺激THP-1 活化的能力,而且,在相同刺激比例下,L.Crispatus 活菌具有比死菌更强的免疫刺激能力,表现为明显上调THP-1 细胞表面标志CD40、CD80、CD86、 CD1a、CCR6 与CD324 的表达水平,同时可诱导活化THP-1 上调表达Th1 型细胞因子。通过FITC-Dextran 吞噬实验,我们发现,经过L.Crispatus 刺激的THP-1 细胞,其吞噬外来抗原的能力明显下降,但尚未检测到经过活化的THP-1 细胞刺激T 细胞增殖的能力。通过流式细胞术分析的方法,我们检测了TLR1、TLR2、TLR4 与TLR6 在不同的刺激分化阶段的表达水平,结果表明,THP-1 主要通过TLR2 与TLR6 识别女性生殖道L.Crispatus。综上所述,本研究首先通过对DC 体外分化成熟的最短时程的分析,确立了快速诱导DC 的最佳方法,进而利用芯片技术,研究了快速诱导DC 的mi/mRNA 表达谱,揭示了DC 体外分化发育过程中可能的调控途径,为进一步研究DC 的基础生物学提供了恰当的模型和具有指向性的线索。同时,通过与DC 前体THP-1 的共同培养体系,证实了生殖道共生乳酸杆菌的免疫调节作用,为以乳酸杆菌为载体的生殖道粘膜免疫疫苗的研究和应用提供了实验依据

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尽管体细胞核移植(somatic cell nuclear transfer, SCNT)技术仍然处于 起步发展阶段,但是随着体细胞核移植技术在近些年来的飞速发展,人们已经得 到了多种哺乳动物体细胞核移植的存活后代。体细胞核移植技术在生物医药、农 业及其它领域的应用显示了这项技术的巨大发展前景。另一方面,人们发现体细 胞核移植效率低下并且体细胞克隆动物存在许多缺陷,这些主要是由于核移植技 术,供体细胞选择,体外培养系统以及卵母细胞的状态等的差异导致的。本研究 主要围绕着这些因素在体细胞核移植过程中对于克隆胚胎植入前后发育的影响 而开展,目的在于提高体细胞核移植的效率。 实验一,研究了几个因素对克隆胚胎发育和克隆效率的影响,为提高体细胞 核移植效率提供一些依据。这部分研究主要包括四倍体半克隆小鼠研究和蛋白酶 体抑制剂在克隆胚胎和孤雌激活胚胎发育中的影响。四倍体体细胞半克隆 (tetraploid semi-cloned , TSC)胚胎的体外发育结果表明,虽然TSC 胚胎可 能避免二倍体半克隆胚胎发育过程中的非整倍体现象,但是仍然不能形成胎儿。 另外,利用蛋白酶体抑制剂MG132 处理克隆胚胎的结果表明,虽然MG132 通过抑 制成熟促进因子(maturation promoting factors,MPF)活性的降低可以提高 克隆胚胎的体外发育率,但是没有改变克隆胚胎的质量。 实验二,研究了克隆技术在克隆胚胎构建和发育上的影响。首先,我们研究 了完整颗粒细胞注射到卵母细胞中所引起的变化。我们发现完整的颗粒细胞注入 到卵母细胞中之后很快引起细胞膜裂解和细胞核碎裂,从而导致激活后重构胚胎 的碎裂。这一实验表明完整供体细胞核注入的方法不适用于小鼠体细胞克隆。接 下来我们研究了不同的核移植技术――利用piezo 的直接注射法(piezoelectric microinjection,PEM)和电融合法(Electrofusion,EF)――对植入前后的克隆胚 胎以及出生后的克隆动物的影响。研究的结果发现,在PEM 法中,提高piezo 脉 冲的强度会导致供体细胞核DNA 断裂增加,使植入前克隆胚胎的细胞数目减少, 凋亡增加,从而降低克隆胚胎的质量。相反,在用EF 法产生的胚胎中细胞核DNA 的断裂很少,克隆胚胎质量相对较好。实验的结果表明,由于两种克隆技术利用 的原理不同,会对克隆胚胎的发育产生一定的影响,从而改变克隆的效率。 实验三,研究了猕猴体细胞克隆胚胎早期发育过程中细胞核内有丝分裂器蛋 白[Nuclear Mitotic Apparatus Protein,NuMA]的表达和分布。尽管在有些猕猴体 细胞核移植胚胎中没有检测到NuMA 的正确表达和分布并且有些胚胎出现了微 管组装异常,但是大多数猕猴体细胞核移植胚胎具有正常的NuMA 蛋白表达和 正常的核型。通过改进操作技术我们得到了可以发育到正常囊胚的猕猴体细胞核 移植胚胎。这些结果提示猕猴SCNT 胚胎发育失败的原因不是NuMA 等重要蛋 白的缺失。

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通过趾骨切片可以准确鉴定年龄,了解一个物种的最长寿命,也为我们研究确定一个物种的生长特点、性成熟期,以及一个地区一个物种的年龄结构、种群生态(Marnell,1998)和群落生态提供重要信息(Morrison,et a1.,2004)。 本论文使用骨骼鉴龄法对中国浙江省宁波市北仑瑞岩寺林场的镇海棘螈(Echinotriton chinhaiensis)雌性繁群进行了年龄结构研究。结果显示:第一次参加繁殖的年龄为3龄;繁群中数量占优势的是5龄、6龄。而在6龄以后参加繁殖的雌性个体数便开始随着年龄的增大而逐渐减少。参加繁殖的雌性年龄最大个体为8龄。平均年龄为5.13龄。同时对其年龄和头体长、体全长的相关性检验,发现其年龄与头体长和体全长不相关,镇海棘螈雌性的生长方式表现为性成熟后能量主要用于繁殖。 另外,对李子坪大凉疣螈(Tylototriton taliangensis) 雄性繁群进行了年龄结构研究。结果显示:大凉疣螈雄性第一次参加繁殖的年龄为4龄;繁群中数量占优势的是5龄、6龄、7龄。而在7龄以后参加繁殖的雄性个体数便开始随着年龄的增大而逐渐减少。参加繁殖的雄性中年龄最大的个体为10龄。平均年龄为6.7龄。对其年龄和头体长、体全长的相关性检验,发现其年龄与头体长和体全长不相关,大凉疣螈雄性生长特点也表现为性成熟后生长缓慢的特点。 研究材料方面,本文采用野外采样与标本馆标本相结合的方式获得了中国蝾螈科2个重要保护物种繁殖群体的剪(指)趾材料,使得建立于其上的年龄结构工作更加可靠、更加具有代表性。 此外,本论文讨论了镇海棘螈瑞岩寺种群繁殖总量年度间的差异及其产生原因。将1998、1999、2000、2008、2009年镇海棘螈(Echinotriton chinhaiensis) 瑞岩寺种群的繁殖量进行比较,发现虽然雌性平均窝卵数比较稳定,但繁殖总量小于1998、1999、2000年任何一年总产卵量的50%。对2008年镇海棘螈繁殖量大幅下降的原因分析发现, 2007年9、10月影响严重台风的两次强台风、瑞岩寺景区开发等因素可能是造成近年该种群繁殖量大幅下降的原因。而2008年初50年不遇的低温是否影响镇海棘螈的繁殖值得进一步追踪研究。2009年繁殖量较2008年没有明显的增长,可能是由于2007年的台风影响了其繁殖营养的积累。台风的影响可能存在滞后现象,对此有待进一步监测证明。 本研究首次对中国蝾螈科物种进行的年龄结构鉴定,为进一步了解中国蝾螈科动物的种群生态打下了坚实的基础。 Using skeletochronology, we can know the life span of a species, age of reaching sexual mature, and of course age structure, which are vital(Morrison,et a1.,2004). Skeletochronology was performed on Echinotriton chinhaiensis Ruiyansi female population. The result shows that: The oldest individuals were 8 years old and the youngest ones were 3 years old. Individuals of age class 5(39.13%) and 6(21.74%) were most numerous. The number of individuals participated in reproduction decreased with the increase of age after the sixth year. Average age is 5.13 years. There is no correlation between age and body size (SVL and TL). For female chinhai salamander, energy is devoted to reproduction after reaching sexual maturation. While using skeletochronology to study Tylototriton taliangensis Liziping male population, the oldest individuals is 10 years old, and the youngest ones is 4 years old. Individuals of the age class 5, 6, and 7 dominat this population. The number of individuals decrease with the increase of age also after the seventh year. Average age is 6.7 years old in this population. there is also no correlation between age and body size (SVL and TL).It turned out that T. taliangensis tend to grow slowly after reaching sexual maturation. In this thesis, specimens from both wild and museum were used to gain enough toe clipping samples. A big sample size guarantees the reliability of this study. In the meantime, E. chinhaiensis’s annual reproduction of the year 1998, 1999, 2000 ,2008,and 2009 was compared. The result shows there is a huge decline in E. chinhaiensis’s annual reproduction in 2008,even the egg clutch is very stable. After analyzing, it turned out the huge decline in 2008 was probably caused by typhoon in 2007, besides the effect of tourism development and cash crop planting. While the impact of extreme weather of 2008 on reproduction needs further investigation. In the year 2009, there is no obvious increase in annual reproduction. It maybe due to lasting impact of typhoon in 2007. It is the first age-structure study on these two Chinese salamanders. A solid foundation was laid for further population ecology study of these two species.

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The ovaries of Kun-Ming strain mice (3 weeks) were irradiated with different doses of C-12(6+) ion in the Bragg peak or the plateau region. At 10th day after irradiation, ovarian and uterine weights were measured: normal and atretic (identified with the oocyte to be degenerating or absent) primordial, primary and preantral follicles were identified in the largest cross-section of each ovary. Percentage (%) of normal follicles of each developmental stage of oogenesis was calculated. The data showed that compared to controls, there was a dose-related decrease in percentage of normal follicles in each developmental stage. And the weights of ovary and uterus were also reduced with doses of irradiation. Moreover, these effects were much more significant in the Bragg peak region and the region close to the Bragg peak than in the beam's entrance (the plateau region). Radiosensitivity varied in different follicle maturation stages. Primordial follicles, which are thought to be extremely sensitive to ionizing irradiation, were reduced by 86.6%, while primary and preantral follicles reduced only by 72.5% and 61.8% respectively, by exposure with 6 Gy of C-12(6+) ion in the Bragg peak region and the region close to the Bragg peak. The data suggested that due to their optimal depth-dose distribution in the Bragg peak region, heavy ions are ones of the best particles for radiotherapy of tumors located next of vital organs or/and surrounded by normal tissues, especially radiosensitive tissues such as gonads.

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FUNCTIONAL-FORM GROUPS; RED ALGAE; ATLANTIC SALMON; NEW-HAMPSHIRE; NITROGEN; PHOSPHORUS; RHODOPHYTA; TEMPERATURE; NUTRIENTS; KJELLMAN

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The precociously sexual maturation in large yellow crocker Pseudosciaena crocea has become a serious problem. In an attempt to solve this problem, the production of sterile triploids could be an effective strategy. In this study, triploid P. crocea was obtained by subjecting fertilized eggs to pressure shock. Flow-cytometry analysis was used to assess ploidy level. In terms of triploid rate and hatching rate, the optimal conditions of pressure shock for triploidy induction in P. crocea were 7500 psi for 3 min shock at 3 min after fertilization at 20 degrees C. With the application of these parameters, 100% triploid fish were produced. During the first rearing year, triploid P. crocea had a similar growth performance compared with its diploid counterpart before the age of 8 months and showed a significant advantage at the age of 10 and 12 months in body weight and body length (P < 0.05). At the age of 12 months, the carcass weight of triploids was markedly higher than that of diploid control, and gonadal somatic index was significantly lower than that of their diploid control. During the first rearing year, survival in triploid group was 76.44%, inferior to its diploid control (83.21%).

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Nets in traditional Porphyra mariculture are seeded with conchospores derived from the conchocelis phase, and spend a nursery period in culture tanks or calm coastal waters until they reach several centimeters in length. Some species of Porphyra can regenerate the foliose phase directly through asexual reproduction, which suggests that the time, infrastructure, and costs associated with conchocelis culture might be avoided by seeding nets with asexual spores. Here, we present work from a short-term mariculture study using nets seeded with asexual spores (neutral spores) of a native Maine species of Porphyra. Porphyra umbilicalis (L.) Kutzing was selected for this proof of concept research because of its reproductive biology, abundance across seasons in Maine, and evidence of its promise as a mariculture crop. We studied the maturation, release, and germination of the neutral spores to develop an appropriate seeding protocol for nets, followed by development of a nursery raceway to provide an easily manipulated environment for the seeded nets. Neutral spores were produced throughout the year on the central Maine coast,however, there was a temporal variability in the number and survival of released neutral spores, depending upon thallus position in the intertidal zone. Small thalli were strictly vegetative, but most thalli reproduced by neutral spores- sexual reproduction was absent. Neutral spores germinated quickly at 10 and 15 'C, but germination was delayed at 5 degrees C. Unlike some algal zygotes and spores, neutral spores of R umbilicalis required light to germinate; however, irradiances of 25 and 100 mu mol photons M-2 S-1 were equally sufficient for germination. Rafts of seeded nets were deployed in Cobscook Bay, Maine, at two distances from salmon aquaculture pens and at a control site on a nearby, fallow aquaculture site (no salmon). There was no difference in nitrogen content of harvested thalli; however, both the density and the surface area of harvested thalli were different among the sites. The possible causes of these differences are discussed in the context of potential use of P umbilicalis in IMTA. (C) 2007 Elsevier B.V. All rights reserved.

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To understand the molecular events of ovarian development in penaeid shrimp, RNA arbitrarily primed polymerase chain reaction (RAP-PCR) was used to identify differentially expressed genes during ovarian maturation in Metapenaeus ensis. From a screening of 700 clones in a cDNA library of the shrimp ovary by the products of RAP-PCR of different maturation stages, 91 fragments with differentially expressed pattern as revealed by dot-blot hybridization were isolated and sequenced. Forty-two of these fragments show significant sequence similarity to known gene products and the differentially expressed pattern of 10 putative genes were further characterized via Northern hybridization. Putative glyceraldehyde-3-phosphate dehydrogenase and arginine kinase are related to provision of energy for active cellular function in oocyte development. Translationally controlled tumor protein, actin, and keratin are related to the organization of cytoskeleton to accomplish growth and development of oocytes. High mobility group protein DSP1, heat shock protein 70, and nucleoside diphosphate kinase may act as repressors before the onset of ovarian maturation. Peptidyl-prolyl cis-trans isomerase and glutathione peroxidase are related to the stabilization of proteins and oocytes. This study provides new insights on the molecular events in the ovarian development in the shrimp.

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Myogenin is a bHLH transcription factor of the MyoD family. It plays a crucial role in myoblast differentiation and maturation. We report here the isolation of flounder myogenin gene and the characterization of its expression patterns. Sequence analysis indicated that flounder myogenin shared a similar structure and the conserved bHLH domain with other vertebrate myogenin genes. Flounder myogenin gene contains 3 exons and 2 introns. Sequence alignment and phylogenetic showed that flounder myogenin was more homologous with halibut (Hippoglossus hippoglossus) myogenin and striped bass (Morone saxatilis) myogenin. Whole-mount embryo in situ hybridization revealed that flounder myogenin was first detected in the medial region of somites that give rise to slow muscles, and expanded later to the lateral region of the somite that become fast muscles. The levels of myogenin transcripts dropped significantly in matured somites at the trunk region. Its expression could only be detected in the caudal somites, which was consistent with the timing of somite maturation. Transient expression analysis showed that the 546 bp flounder myogenin promoter was sufficient to direct muscle-specific GFP expression in zebrafish embryos. (c) 2007 Elsevier Inc. All rights reserved.

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Fully grown oocytes of Apostichopus japonicus have a cytoplasmic protuberance where the oocyte attaches to the follicle. The protuberance and the oolamina located on the opposite side of the oocyte indicate the animal-vegetal axis. Two pre-meiotic centrosomes are anchored to the protuberance by microtubules between centrosomes and protuberance. After meiosis reinitiation induced by DTT solution, the germinal vesicle (GV) migrates towards the protuberance. The GV breaks down after it migrates to the oocyte membrane on the protuberance side. The protuberance then contracts back into the oocyte and the first polar body extrudes from the site of the former protuberance. The second polar body forms beneath the first. Thus the oocyte protuberance indicates the presumptive animal pole well before maturation of the oocyte.

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Triploid Penaeus (Fenneropenaeus) chinensis was successfully produced by heat shock. Their metamorphosis, the relationship between body weight and length and difference in appearance between triploids and their diploid siblings under laboratory culture were studied. Hematological studies showed a smaller number of haemocytes, but larger cell volume, in triploids than in diploids. Triploid shrimp did not show higher growth during the immature stage, but exhibited superior growth during the maturation stage. Characteristics of reproductive organs indicated that triploid shrimp may be sterile and sex ratio can be changed through triploidization of shrimp. This paper summarizes the progress made in triploid shrimp research which would be helpful in understanding more about triploids of crustaceans. (c) 2006 Elsevier B.V. All rights reserved.

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Specification and differentiation of skeletal muscle cells are driven by the activity of genes encoding members of the myogenic regulatory factors (MRFs). In vertebrates, the MRF family includes MyoD, Myf5, myogenin, and MRF4. The MRFs are capable of converting a variety of nonmuscle cells into myoblasts and myotubes. To better understand their roles in fish muscle development, we isolated the MyoD gene from flounder (Paralichthys olivaceus) and analyzed its structure and patterns of expression. Sequence analysis showed that flounder MyoD shared a structure similar to that of vertebrate MRFs with three exons and two introns, and its protein contained a highly conserved basic helix-loop-helix domain (bHLH). Comparison of sequences revealed that flounder MyoD was highly conserved with other fish MyoD genes. Sequence alignment and phylogenetic analysis indicated that flounder MyoD, seabream (Sparus aurata) MyoD1, takifugu (Takifugu rubripes) MyoD, and tilapia (Oreochromis aureus) MyoD were more likely to be homologous genes. Flounder MyoD expression was first detected as two rows of presomitic cells in the segmental plate. From somitogenesis, MyoD transcripts were present in the adaxial cells that give rise to slow muscles and the lateral somitic cells that give rise to fast muscles. After 30 somites formed, MyoD expression decreased in the somites except the caudal somites, coincident with somite maturation. In the hatching stage, MyoD was expressed in other muscle cells and caudal somites. It was detected only in muscle in the growing fish.

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采用体外药物诱导的方法,研究了5-羟色胺(5-hydroxytryptamine,5-HT)诱导的硬壳蛤卵母细胞成熟过程中cAMP信号通路的作用。结果表明,5-HT (0.01—100µM)均能够显著地诱导硬壳蛤卵母细胞的成熟。磷酸二酯酶抑制剂—咖啡因、茶碱和IBMX(3-异丁基-1-甲基黄嘌呤)可以单独抑制卵母细胞的自发成熟,但效果不显著。10mM的咖啡因和茶碱以及5mM的IBMX能够显著地抑制5-HT的诱导效果。dbcAMP(双丁酰基环腺苷一磷酸)不但能够抑制卵母细胞的自发成熟,而且还可以抑制5-HT诱导的成熟。因此,cAMP信号通路参与了5-HT诱导的硬壳蛤卵母细胞的成熟过程,并且该信号通路起着负调控的作用。 研究了PLC(磷脂酶C)和PKC(蛋白激酶C)的激活剂/抑制剂对5-羟色胺诱导的卵母细胞成熟的影响。高浓度的新霉素(PLC抑制剂)可以抑制5-HT诱导的卵母细胞的成熟,而DMBA(9,10-Dimethy-1,2-benzanthracene,9,10–二甲基胆蒽,PLC激活剂)则能够促进成熟。PMA(phorbol 12-myristate 13-acetate,佛波十四烷酸乙酸酯,PKC激活剂)能够抑制5-HT诱导的成熟,而Spingosine(PKC抑制剂)则可以促进卵母细胞的成熟。从而推测,5-HT诱导的卵母细胞成熟需要磷脂酰肌醇信号通路的激活。PLC浓度的降低能够抑制5-HT诱导的卵母细胞成熟;PKC浓度的降低则会促进卵母细胞的成熟。因此,在硬壳蛤卵母细胞的成熟过程中,PLC起促进的作用,DAG(二酰肌甘油)–PKC通路则起抑制的作用。 细胞外高浓度Ca2+能够促进硬壳蛤卵母细胞的成熟,Ca2+离子载体A23187也可以促进硬壳蛤卵母细胞的成熟。1-100µM异搏定(Verapamil,钙离子通道阻断剂)能够抑制卵母细胞的成熟,而100µM的Verapamil能够完全抑制其成熟。上述结果表明细胞外Ca2+对硬壳蛤卵母细胞的成熟是必需的,而且起到促进卵母细胞成熟的作用。三氟拉嗪(TFP,Ca2+与CaM结合的拮抗剂)能够抑制卵母细胞的成熟,高浓度的三氟拉嗪(1mM)能够完全抑制卵母细胞的成熟。说明CaM起到促进卵母细胞成熟的作用。可见,Ca2+通过与CaM的相互作用,共同起到促进硬壳蛤卵母细胞成熟的作用。 5-HT诱导成熟的卵母细胞可以完成受精过程,其受精过程以及幼虫发育情况与正常受精发育过程类似,没有显著差异。高浓度的新霉素可以抑制受精过程,而茶碱和咖啡因对受精没有影响。从而推测,磷脂酰肌醇信号通路参与了硬壳蛤卵母细胞的受精过程,而cAMP信号通路可能没有参与受精过程。 发现硬壳蛤的性腺发育与我国常见的双壳类如泥蚶相似。硬壳蛤卵母细胞中卵黄粒主要由线粒体、高尔基液泡、内质网和微吞饮泡形成。