厚壳贻贝一种新型贝壳胶原蛋白的重组表达与功能分析

贝壳是一种具有优异力学性能的生物硬组织,贝壳基质蛋白质对贝壳的形成具有重要意义。厚壳贻贝(Mytilus coruscus)贝壳中发现一种类似胶原蛋白质的新型贝壳基质蛋白质,命名为collagen-like protein 2（CLP-2）。然而,该蛋白质的结构与功能以及对贝壳形成的影响机制尚不清楚。为此,本研究对CLP 2开展了序列分析;进一步采取密码子优化结合原核重组表达策略,开展了CLP-2的重组表达;在此基础上分析了重组CLP-2对酸钙结晶的诱导、结晶速率抑制以及碳酸钙结合能力。对CLP-2的序列分析结果表明,该蛋白质序列中含有信号肽及两个Von Willebrand factor A（VWA）结构域。CLP-2在数据库中尚无高同源性蛋白质存在,表明这是一种较为新颖的贝壳基质蛋白。所获得的重组CLP-2对碳酸钙体外结晶表现出明显的诱导作用,扫描电镜以及傅里叶红外光谱结果表明,重组CLP-2可诱导碳酸钙晶体的形貌由立方体形转化为球形,并在高浓度下进一步转化为哑铃形;同时,重组CLP-2可促使碳酸钙晶体的晶型由方解石型向文石型转化;重组CLP-2在体外具有碳酸钙晶体结合作用;此外,重组CLP-2能显著抑制碳酸钙晶体的结晶速度（P<0.01）,并具有浓度依赖性。上述结果表明,厚壳贻贝贝壳CLP-2蛋白质在贝壳,特别是文石型肌棱柱层的生物矿化过程中具有重要作用。上述研究为深入了解贻贝贝壳的形成机制,以及胶原类蛋白质对生物矿化过程的影响奠定了基础。     

珍珠颜色和贝壳珍珠层颜色研究进展

颜色及其色度均一性是衡量珍珠价值的重要指标之一。珍珠颜色及贝壳珍珠层颜色的研究涉及多个学科领域,研究表明,珍珠的颜色与制片蚌外套膜对应的珍珠层颜色相一致,而蚌的珍珠层颜色主要由遗传因素决定。现有的研究资料对珍珠层颜色形成的机理虽然还不能给出一个系统、合理的诠释,但金属元素、卟啉、类胡萝卜素和物理结构等因素可能和珍珠层颜色形成密切相关,珍珠层中含有少量以蛋白质为主的有机基质,这些蛋白调控珍珠层的结构和颜色的形成,可能是解释珍珠层颜色形成机理的关键。本文对珍珠颜色和贝壳珍珠层颜色研究进展进行系统综述,探讨珍珠颜色的影响因素及相互关联,旨在为进一步研究珍珠和贝壳珍珠层颜色提供借鉴与思路。     

外套膜转录物组分析揭示尿素在贻贝耐受海水酸化中的作用

海洋酸化是目前地球面临的主要环境问题之一,对海洋矿化生物的生存带来严重威胁。贝类是目前海水养殖的主要物种,海洋酸化会对贝壳的生物矿化过程产生抑制,因而对贝类养殖业的发展带来严重影响。前期研究中已发现,尿素对贻贝贝壳的形成具有辅助作用,推测尿素有助于贻贝在海洋酸化背景下的生存。为进一步探究尿素通过何种分子机制对贻贝耐受海洋酸化产生积极影响,以厚壳贻贝外套膜为研究对象,采用转录物组学策略分析了尿素添加对贻贝外套膜组织在酸化海水中的基因表达量变化的影响。结果表明,尿素添加对贻贝外套膜在酸化条件下的转录物组变化具有逆转趋势,可抑制外套膜中受酸化胁迫而激活的细胞自噬、凋亡、以及免疫应激相关通路;同时,也诱导了部分贝壳基质蛋白质表达量的上调,从而有助于维持贻贝在酸化条件下的生物矿化过程。上述研究有助于了解贻贝对海洋酸化的耐受性机制,也为后续贝类养殖业在海洋酸化背景下的健康发展提供了新的思路。     

人肺腺癌细胞A—549和正常细胞HBE的蛋白质组差异分析

为了研究人肺腺癌细胞A 5 49和正常细胞HBE的蛋白质组差异 ,用固相pH梯度双向凝胶电泳分离人肺腺癌细胞系A 5 49和正常细胞HBE的总蛋白质 ,银染显色 ,PDQuest 2 DE软件分析 ,对部分差异蛋白质点进行基质辅助激光解吸电离飞行时间质谱 (MALDI TOF MS)测定其胶内酶解后的肽质指纹图谱 ,用PeptIdent软件查询SWISS PROT数据库。结果获得了分辨率和重复性均较好的双向电泳银染图谱 ,图象分析探测到A 5 492 DE图谱的平均蛋白质点数为 (890± 38)个 ,HBE的平均蛋白质点数为 (75 7± 2 7)个 ,不同胶间蛋白质点的位置偏差在IEF方向为 (2 .85± 0 .48)mm ,在SDS PAGE方向为 (2 .6 9± 0 .37)mm。差异表达分析发现A 5 49和HBE图谱有5 35个蛋白质点相互匹配 ,其中A 5 49有 35 5个未被匹配 ,HBE中有 2 2 2个未被匹配 ;对A 5 49和HBE中的 18个差异蛋白质点分别进行肽质指纹分析 ,经数据库查询 ,初步鉴定为一些与物质代谢、细胞因子、信号转导有关的蛋白质。提示人肺腺癌细胞A 5 49和正常细胞HBE的蛋白质组具有差异 ,这种蛋白质组的差异分析有助于进一步研究肺腺癌的相关蛋白质及分子标记物     

帕金森病和正常人外周血单个核细胞的蛋白质组差异分析

目的:通过研究帕金森病和正常外周血单个核细胞(PBMC)的蛋白质组差异,初步探讨外周免疫系统与帕金森病的病理联系.方法:用固相pH梯度双向凝胶电泳分离人帕金森病和正常单个核细胞总蛋白质,考马斯亮蓝染色,PDQuest 2-DE软件分析,对部分差异蛋白质点进行基质辅助激光解吸电离飞行时间质谱(MALDI-TOF-MS)测定其胶内酶解后的肽质指纹图谱,用Mascot查询系统查询SWISS-PROT数据库.结果:获得了分辨率和重复性均较好的双向电泳考染图谱,对其中的21个差异蛋白质点分别进行肽质指纹分析,经数据库查询,初步鉴定为一些与蛋白降解、抗氧化应激、信号转导、细胞骨架、细胞周期调控等有关的蛋白质.结论:建立了帕金森病PBMC的双向凝胶电泳图谱,提示帕金森病和正常的PBMC的蛋白质表达具有差异.     

非肌层浸润性膀胱癌患者TURBT术后吉西他滨与表柔比星膀胱灌注化疗的疗效比较及复发的危险因素分析

摘要 目的：对比非肌层浸润性膀胱癌（NMIBC）患者经尿道膀胱肿瘤电切术（TURBT）后吉西他滨与表柔比星膀胱灌注化疗的临床疗效,并分析复发的危险因素。方法：纳入徐州医科大学附属连云港医院2018年1月至2020年1月期间接收的NMIBC患者120例,均接受TURBT治疗。根据化疗用药方式的不同将120例NMIBC患者分为表柔比星组（n=58,表柔比星治疗）和吉西他滨组（n=62,吉西他滨治疗）,对比表柔比星组、吉西他滨组的免疫功能、肿瘤标志物变化,观察不良反应发生率及1年复发情况。采用多因素Logistic回归分析NMIBC患者行TURBT后复发的危险因素。结果：表柔比星组、吉西他滨组治疗后CD3⁺、CD4⁺、CD4⁺/CD8⁺升高,且吉西他滨组高于表柔比星组（P<0.05）;CD8⁺下降,且吉西他滨组低于表柔比星组（P<0.05）。表柔比星组、吉西他滨组治疗后癌胚抗原（CEA）、细胞角蛋白19（CK19）和癌抗原199（CA199）均下降,且吉西他滨组低于表柔比星组（P<0.05）。表柔比星组、吉西他滨组不良反应发生率对比未见统计学差异（P>0.05）。表柔比星组、吉西他滨组1年复发率对比未见统计学差异（P>0.05）。将表柔比星组、吉西他滨组1年后复发的患者总和28例纳为复发组,其余未复发的92例纳为未复发组。单因素分析结果显示：NMIBC患者行TURBT后复发与肿瘤数目、最大肿瘤直径、肿瘤分化分级、临床分期有关（P<0.05）。多因素Logistic回归分析结果显示：肿瘤数目为多发、最大肿瘤直径≧5 cm、肿瘤分化分级为低分化、临床分期为T1期为NMIBC患者行TURBT后复发的危险因素（P<0.05）。结论：与表柔比星化疗相比,吉西他滨化疗可更好的控制肿瘤疾病进展,有效保护机体免疫功能,两种化疗药物下安全性和复发率相接近。同时研究还观察到,复发受到多种因素影响,包括肿瘤数目、最大肿瘤直径、肿瘤分化分级、临床分期。     

翡翠贻贝精子的超微结构

利用透射电镜研究翡翠贻贝 (Pernaviridis)精子的超微结构。精子为典型的原生型 ,包括头部、中段与尾部三部分。头部由顶体和细胞核组成。顶体明显突出呈倒漏斗形。亚顶体腔呈锥形 ,其中的亚顶体物质呈伞状分布 ,中轴一直延伸至核的后端。细胞核近似球形 ,被管状的核前窝几乎分成相似的两部分。 4～ 5个椭圆形的线粒体围绕着中心粒复合体形成精子的中段。中心粒为中空的圆柱形 ,具有卫星体结构。尾部细长 ,轴丝为典型的“9 2”结构。本文讨论了双壳类精子形态的种属间的差异。     

Osteogenic Potency of Nacre on Human Mesenchymal Stem Cells

Nacre seashell is a natural osteoinductive biomaterial with strong effects on osteoprogenitors, osteoblasts, and osteoclasts during bone tissue formation and morphogenesis. Although nacre has shown, in one study, to induce bridging of new bone across large non-union bone defects in 8 individual human patients, there have been no succeeding human surgical studies to confirm this outstanding potency. But the molecular mechanisms associated with nacre osteoinduction and the influence on bone marrow-derived mesenchymal stem cells (BMSC’s), skeletal stem cells or bone marrow stromal cells remain elusive. In this study we highlight the phenotypic and biochemical effects of Pinctada maxima nacre chips and the global nacre soluble protein matrix (SPM) on primary human bone marrow-derived stromal cells (hBMSCs) in vitro. In static co-culture with nacre chips, the hBMSCs secreted Alkaline phosphatase (ALP) at levels that exceeded bone morphogenetic protein (rhBMP-2) treatment. Concentrated preparation of SPM applied to Stro-1 selected hBMSC’s led to rapid ALP secretions, at concentrations exceeding the untreated controls even in osteogenic conditions. Within 21 days the same population of Stro-1 selected hBMSCs proliferated and secreted collagens I–IV, indicating the premature onset of an osteoblast phenotype. The same SPM was found to promote unselected hBMSC differentiation with osteocalcin detected at 7 days, and proliferation increased at 7 days in a dose-dependent manner. In conclusion, nacre particles and nacre SPM induced the early stages of human bone cell differentiation, indicating that they may be promising soluble factors with osteoinductive capacity in primary human bone cell progenitors such as, hBMSC’s.     

Spermatogenesis of the green-lipped mussel Perna viridis with dual patterns of acrosome and tail development in spermatids

Spermatogenesis in the mussel Perna viridis was studied by electron microscopy. Results demonstrated that cytological development in spermatogonia and spermatocytes was similar to that previously described in other Mytilidae. Acrosome formation began with the arising of proacrosomal vesicles in spermatogonia. The abundance of proacrosomal vesicles increased in spermatocytes, which were flagellated. However, during spermiogenesis, dual patterns of acrosome development as well as flagellum development could be found among spermatids in a male gonad. The two lines of acrosome formation in spermatids ultimately gave rise to morphologically similar acrosomes. The two lines of flagellum development in spermatids resulted in the formation of sperm cells with either a typically posteriorly directed tail or an anteriorly directed tail. Received: 22 July 1998 / Accepted: 12 September 1998     

Byssus of the Green-Lipped Mussel <Emphasis Type="Italic">Perna viridis</Emphasis> (Linnaeus) as a Biomonitoring Material for Zn

Recently, Yap et al. (2003) suggested that the byssus of the green-lipped mussel Perna viridis can be a biomonitoring material for Zn although further validation is required. In this work, we did a simple correlation study between Zn concentrations in the byssus (and soft tissue) and in different geochemical fractions of the sediment. A significant (P < 0.01) Pearsons correlation coefficient (R = 0.84) between the Zn concentrations in the byssus and soft tissue indicated that the Zn level in the byssus is highly correlated to its level in the soft tissue and that the byssus could act as an excretion route for Zn. Higher R-values were found between the byssus-easily or freely, leachable and exchangeable, byssus-acid-reducible, byssus-oxidizable-organic and byssus-nonresistant fractions of the sediment, and the byssus-Zn concentration in the total sediment when compared to those found between the soft tissue and the same geochemical fractions. This indicated that the byssus was more reflective of Zn contamination in the field environment than the soft tissue. Therefore, the data further support the use of the byssus as a biomonitoring material for Zn as was originally suggested by Yap et al. [3].Original English Text Copyright © 2005 by Biologiya Morya, Yap, Ismail, Tan.This article was submitted by the authors in English.     

Zona Localization of Shell Matrix Proteins in Mantle of <Emphasis Type="Italic">Haliotis tuberculata</Emphasis> (Mollusca,Gastropoda)

Organic matrix from molluscan shells has the potential to regulate calcium carbonate deposition and crystallization. Control of crystal growth thus seems to depend on control of matrix protein secretion or activation processes in the mantle cells, about which little is known. Biomineralization is a highly orchestrated biological process. The aim of this work was to provide information about the source of shell matrix macromolecule production, within the external epithelium of the mantle. An in vivo approach was chosen to describe the histologic changes in the outer epithelium and in blood sinus distribution, associated with mantle cells implicated in shell matrix production. Our results characterized a topographic and time-dependent zonation of matrix proteins involved in shell biomineralization in the mantle of Haliotis.     

The Biomineralization Proteome: Protein Complexity for a Complex Bioceramic Assembly Process

There are over 62 different biominerals on Earth and a diverse array of organisms that generate these biominerals for survival. This review will introduce the process of biomineralization and the current understanding of the molecular mechanisms of mineral formation, and then comparatively explore the representative secretomes of two well‐documented skeletal systems: vertebrate bone (calcium phosphate) and invertebrate mollusk shell (calcium carbonate). It is found that both skeletal secretomes have gross similarities and possess proteins that fall into four functional categories: matrix formers, nucleation assisters, communicators, and remodelers. In many cases the mineral‐associated matrix former and nucleation assister sequences in both skeletal systems are unique and possess interactive conserved globular domains, intrinsic disorder, post‐translational modifications, sequence redundancy, and amyloid‐like aggregation‐prone sequences. Together, these molecular features create a protein‐based environment that facilitates mineral formation and organization and argue in favor of conserved features that evolve from the mollusk shell to bone. Interestingly, the mollusk shell secretome appears to be more complex compared to that of bone tissue, in that there are numerous protein subcategories that are required for the nucleation and organization of inner (nacre) and outer (prismatic) calcium carbonate regions of the shell. This may reflect the organizational and material requirements of an exoskeletal protective system.     

Settlement and growth of the green mussel Perna viridis (L.) in coastal waters: influence of water velocity

Green mussels Perna viridis were observed to be a major foulant in the seawater intake tunnel of a coastal power station. Field experiments were carried out to ascertain what factors were responsible for the successful colonisation by mussels. Two adjacent stations (25 m apart) were selected, one representing the coastal waters and the other representing the intake screens (with higher water velocity). Gonadal activity, larval abundance, spat settlement and growth rate of the mussels were monitored at monthly intervals for a total period of two years. The results showed that the breeding activity of the mussels at the study area is influenced largely by temporal distribution of seawater temperature. However, ensuing larval availability in the coastal waters is more dependent on food availability. On the other hand, spat settlement and growth rate are predominantly influenced by water flow, probably as a result of increased propagule and food flux rate at higher water velocities. Higher water velocity at the intake screens also contributed to mussel dominance by preventing settlement of many potential competitors.     

A Novel Matrix Protein p10 from the Nacre of Pearl Oyster (Pinctada fucata) and Its Effects on Both CaCO3 Crystal Formation and Mineralogenic Cells

A novel matrix protein, designated as p10 because of its apparent molecular mass of 10 kDa, was isolated from the nacreous layer of pearl oyster (Pinctada fucata) by reverse-phase high-performance liquid chromatography. In vitro crystallization experiments showed that p10 could accelerate the nucleation of calcium carbonate crystals and induce aragonite formation, suggesting that it might play a key role in nacre biomineralization. As nacre is known to contain osteogenic factors, two mineralogenic cell lines, MRC-5 fibroblasts and MC3T3-E1 preosteoblasts, were used to investigate the biological activity of p10. The results showed that p10 could increase alkaline phosphatase activity, an early marker of osteoblast differentiation, while the viability of MRC-5 and MC3T3-E1 remained unchanged after treatment of p10. Taken together, the findings led to identification of a novel matrix protein from the nacre of P. fucata that plays a role in both the mineral phase and in the differentiation of the cells involved in biomineralization.     

Chemical cues from predators and damaged conspecifics affect byssus production in the green-lipped mussel perna viridis

Juveniles of the green-lipped mussel Perna viridis (Bivalvia: Mytilidae) were exposed to either chemical cues of damaged conspecifics or predator, including the swimming crab Thalamita danae and the muricid gastropod Thais clavigera. Byssus production was monitored for 48 h but the highest production rate occurred in the first 6 h. Longer and thicker byssal threads with a larger total volume were produced by P. viridis exposed to damaged conspecifics and predators as compared with the control. Numbers of individuals which shed stalks during the experiment varied significantly from 0 to 50%, and with a significantly higher value obtained for the control. Results indicated that byssus production is a plastic response which could be induced by exposure to chemical signals from predators and damaged conspecifics, the latter producing the largest response. Firmer byssal attachment not only reduces predation risk but also non-predation mortality by securing an animal more effectively to its habitat.     

Cues from the predator crab Thalamita danae fed different prey can affect scope for growth in the prey mussel Perna viridis

Clearance rate (CR), absorption efficiency (AE), respiration rate, excretion rate and scope for growth (SFG) were investigated in the green-lipped mussel Perna viridis upon exposure to predatory crabs, Thalamita danae, that had been either starved or maintained on diets with P. viridis or shrimp tissue. The CR and SFG were significantly lower when the mussels were exposed to starved T. danae or those fed with mussels. The differences were observed immediately after the mussels were exposed to the cues (Day 0) and 7 days later. The AE, however, was significantly different among treatments on Day 0, with the highest efficiency being obtained for mussels exposed to crabs maintained on shrimp and followed by the control without any predator cues. Results showed that P. viridis was able to discriminate between predators on different diets and adjust physiological responses according to the level of perceived risk, with growth reduced at higher risks.