全球人类福祉提升的碳强度差异测度：影响因素及空间溢出效应

实现低碳化的人类福祉提升是可持续发展的根本要求，人类福祉提升的碳强度指标是衡量可持续发展程度的新指标。论文使用了人类福祉碳强度指标，应用探索性空间数据分析法分析了全球人类福祉碳强度的时空演进格局，运用空间杜宾模型揭示了全球人类福祉碳强度的影响因素及其空间溢出效应。研究发现：(1)1980—2016年全球人类福祉碳强度明显降低，但在北美洲、欧洲和大洋洲国家与其他区域国家(地区)之间存在显著差距。(2)经济增长、能源消费结构、工业化、资本积累、死亡率等因素提高了全球人类福祉碳强度，贸易依存度则是不断降低全球人类福祉碳强度的主要驱动力。(3)影响全球人类福祉碳强度差异的因素呈现区域异质性，能源消费结构、贸易依存度、工业化、资本积累、死亡率等因素对全球人类福祉碳强度的影响，因其经济发展水平和阶段不同而体现出明显的“南北差异”和不同的空间溢出效应。(4)周边国家的能源消费结构、工业化、资本积累和死亡率等因素会增加本国人类福祉碳强度，但本国人类福祉碳强度也会随着周边国家的经济增长和贸易依存度而降低。     

Global gene expression during the human organogenesis: from transcription profiles to function predictions

Human embryogenesis includes an integrated set of complex yet coordinated development of different organs and tissues, which is regulated by the spatiotemporal expression of many genes. Deciphering the gene regulation profile is essential for understanding the molecular basis of human embryo development. While molecular and genetic studies in mouse have served as a valuable tool to understand mammalian development, significant differences exists in human and mouse development at morphological and genomic levels. Thus it is important to carry out research directly on human embryonic development. Here we will review some recent studies on gene regulation during human embryogenesis with particular focus on the period of organogenesis, which had not been well studied previously. We will highlight a gene expression database of human embryos from the 4(th) to the 9(th) week. The analysis of gene regulation during this period reveals that genes functioning in a given developmental process tend to be coordinately regulated during human embryogenesis. This feature allows us to use this database to identify new genes important for a particular developmental process/pathway and deduce the potential function of a novel gene during organogenesis. Such a gene expression atlas should serve as an important resource for molecular study of human development and pathogenesis.     

Human breast development

This review is intended to give an overview of current knowledge on human breast development. It focuses on the limitations of our understanding on the origins of human breast cancer in the context of this mainly morphological and static assessment of what is known about human breast development. The world literature is very limited and caution is needed in drawing analogies with the mouse. There is an increasing emphasis on research to understand normal stem cells in the breast on the assumption that these are the targets for the initiation of breast cancer. It is thus a priority to understand normal human breast development, but there are major obstacles to such studies mainly due to ethical considerations and to tissue acquisition.     

Differences in Gene Expression between Mouse and Human for Dynamically Regulated Genes in Early Embryo

Infertility is a worldwide concern that can be treated with in vitro fertilization (IVF). Improvements in IVF and infertility treatment depend largely on better understanding of the molecular mechanisms for human preimplantation development. Several large-scale studies have been conducted to identify gene expression patterns for the first five days of human development, and many functional studies utilize mouse as a model system. We have identified genes of possible importance for this time period by analyzing human microarray data and available data from online databases. We selected 70 candidate genes for human preimplantation development and investigated their expression in the early mouse development from oocyte to the 8-cell stage. Maternally loaded genes expectedly decreased in expression during development both in human and mouse. We discovered that 25 significantly upregulated genes after fertilization in human included 13 genes whose orthologs in mouse behaved differently and mimicked the expression profile of maternally expressed genes. Our findings highlight many significant differences in gene expression patterns during mouse and human preimplantation development. We also describe four cancer-testis antigen families that are also highly expressed in human embryos: PRAME, SSX, GAGE and MAGEA.     

关于人类发展的环境容量问题之哲学思考

关于人类发展的环境容量问题之哲学思考陈贻安（北京交通管理干部学院１０１６０１）ＡＰｈｉｌｏｓｏｐｈｉｃＴｈｏｕｇｈｏｎＥｎｖｉｒｏｎｍｅｎｔａｌＣａｐａｃｉｔｙｆｏｒＨｕｍａｎＤｅｖｅｌｏｐｍｅｎｔ．￥ＣｈｅｎＹｉａｎ（ＢｅｉｊｉｎｇＣｏｍｍｕｎｉｃ...     

The ethics of ex utero research on spare 'non-viable' IVF human embryos

In this paper, the focus is not on some particular developmental feature of the human embryo, but rather on the embryo's potential for development tout court. To this end, the moral relevance of the difference between human embryos that have the potential for continued human growth and development and human embryos that do not have this potential is explored and a distinction between viable and non-viable IVF human embryos is introduced. This is followed by a discussion of what is morally wrong with killing to show that none of the concerns associated with the act of killing apply to the destruction of non-viable IVF human embryos. On this basis, it is argued that scientifically and ethically sound research on spare non-viable IVF human embryos may proceed.     

Xenotransplantation Models to Study the Effects of Toxicants on Human Fetal Tissues

Many diseases that manifest throughout the lifetime are influenced by factors affecting fetal development. Fetal exposure to xenobiotics, in particular, may influence the development of adult diseases. Established animal models provide systems for characterizing both developmental biology and developmental toxicology. However, animal model systems do not allow researchers to assess the mechanistic effects of toxicants on developing human tissue. Human fetal tissue xenotransplantation models have recently been implemented to provide human‐relevant mechanistic data on the many tissue‐level functions that may be affected by fetal exposure to toxicants. This review describes the development of human fetal tissue xenotransplant models for testis, prostate, lung, liver, and adipose tissue, aimed at studying the effects of xenobiotics on tissue development, including implications for testicular dysgenesis, prostate disease, lung disease, and metabolic syndrome. The mechanistic data obtained from these models can complement data from epidemiology, traditional animal models, and in vitro studies to quantify the risks of toxicant exposures during human development     

Murine and human IL-7 activate STAT5 and induce proliferation of normal human pro-B cells

The role of IL-7 in lymphoid development and T cell homeostasis has been extensively documented. However, the role of IL-7 in human B cell development remains unclear. We used a xenogeneic human cord blood stem cell/murine stromal cell culture to study the development of CD19+ B-lineage cells expressing the IL-7R. CD34+ cord blood stem cells were cultured on the MS-5 murine stromal cell line supplemented with human G-CSF and stem cell factor. Following an initial expansion of myeloid/monocytoid cells within the initial 2 wk, CD19+/pre-BCR- pro-B cells emerged, of which 25-50% expressed the IL-7R. FACS-purified CD19+/IL-7R+ cells were larger and, when replated on MS-5, underwent a dose-dependent proliferative response to exogenous human IL-7 (0.01-10.0 ng/ml). Furthermore, STAT5 phosphorylation was induced by the same concentrations of human IL-7. CD19+/IL-7R- cells were smaller and did not proliferate on MS-5 after stimulation with IL-7. In a search for cytokines that promote human B cell development in the cord blood stem cell/MS-5 culture, we made the unexpected finding that murine IL-7 plays a role. Murine IL-7 was detected in MS-5 supernatants by ELISA, recombinant murine IL-7 induced STAT5 phosphorylation in CD19+/IL-7R+ pro-B cells and human B-lineage acute lymphoblastic leukemias, and neutralizing anti-murine IL-7 inhibited development of CD19+ cells in the cord blood stem cell/MS-5 culture. Our results support a model wherein IL-7 transduces a replicative signal to normal human B-lineage cells that is complemented by additional stromal cell-derived signals essential for normal human B cell development.     

Understanding Human Lung Development through In Vitro Model Systems

An abundance of information about lung development in animal models exists; however, comparatively little is known about lung development in humans. Recent advances using primary human lung tissue combined with the use of human in vitro model systems, such as human pluripotent stem cell-derived tissue, have led to a growing understanding of the mechanisms governing human lung development. They have illuminated key differences between animal models and humans, underscoring the need for continued advancements in modeling human lung development and utilizing human tissue. This review discusses the use of human tissue and the use of human in vitro model systems that have been leveraged to better understand key regulators of human lung development and that have identified uniquely human features of development. This review also examines the implementation and challenges of human model systems and discusses how they can be applied to address knowledge gaps.     

模式动物与人类疾病的动物模型

围绕疾病所开展的基础研究已成为当今生物医学研究领域中的主要内容,而利用模式动物建立疾病的动物模型已是其研究的重要手段,对疾病的基础研究和转化研究均具有重要意义,已成为影响该领域发展的一个关键因素。我国医学研究领域中加强人类疾病动物模型研究既是一个现实问题,更是一个迫切问题,国家自然科学基金委员会医学科学部将在这方面予以倾斜支持。     

创新公立医院人力资源管理的探索

?????现代医院的竞争力越来越集中于对医院内部核心竞争力的比较,而人力资源管理作为医院核心竞争力的源泉发挥着重要的作用。本文从转变观念、建立科学先进的管理机制,对人力资源进行有效规划、投资、经营,实施人力资源的开发和培养工程等方面,阐述人力资源管理创新举措,使医院在竞争中赢得发展优势。

     

The use of functional human tissues in drug development

Drug development currently depends on animal models to provide an accurate prediction of human physiology and pathophysiology. However, as is clear from clinical trial failures during phases II and III, such in vivo models do not always predict the effects that a drug can elicit in humans. Tests with human tissues, which are obviously considered to be the closest model of human in vivo function, could fill the gap between animal-based tests and trials in patients. Despite clear advantages, logistical and ethical barriers prevent fresh human tissues from being widely used during drug development. Biopta is aiming to make human tissue testing a regular element of drug development, and works to lower the barriers surrounding the availability of tissue and practicalities of experimental work.     

人类文明演化的生态观

自从地球上出现生命以后 ,生命就与环境构成了复杂庞大的生态系统。人类的出现使得生态系统日益复杂化 ,纯粹的天然系统逐渐被打上了人类活动的烙印 ,人类根据自身的需要 ,不断地改变原有的纯自然的生态平衡 ,创造出更适合人类生存、生活和生产的人工生态系统 ,达到新的平衡 ,不断建造了人类文明 ,因此 ,人类文明史实际上是一部人与自然环境、社会环境及心理环境竞争与共生、改造与适应的生态史。1　农业文明的兴衰在旧石器时代末 ,地球上人口总数不到 30 0万 ,到中石器时代也只有 1 0 0 0万 ,这一时期 ,人类还仅仅是自然生态系统食物网中的…     

全球冠状病毒疫苗专利分析

冠状病毒是一类可感染人类和动物的RNA病毒,可引起严重急性呼吸综合征(SARS)和中东呼吸综合征(MERS)等严重疾病。新型冠状病毒是以前从未在人体中发现的冠状病毒新毒株,其人际传播迅速,引起了各国政府的高度重视并积极寻求疫苗防控对策。基于冠状病毒疫苗领域全景专利,在综合对比分析该领域的全部专利的发展趋势、主要国家和主要机构的专利产出的同时,重点揭示了其中的人用相关疫苗的发展与分布情况以及重点分析了人用疫苗产品的研发现状,以期为我国冠状病毒疫苗领域的科研工作者和管理决策者提供参考数据。     

Identification of Novel Genes Differentially Expressed in PMA-induced HL-60 Cells Using cDNA Microarrays

Identification of normal growth and differentiation-inducing proteins and their interaction in normal development have made it possible to elucidate the molecular basis of normal development and the mechanisms uncoupling growth and differentiation during tumor development. The development of cancer and the experimental reversal of tumorigenicity are accompanied by complex changes in patterns of gene expression. cDNA microarrays provide a powerful tool for studying these phenomena. In the present study, a high-density microarray of human cDNA elements was used to search for differences in gene expression associated with differentiation of human promyelic leukemia HL-60 cells. Microarrays containing 3,063 human cDNAs were printed on glass slides with high-speed robotics. These DNA 'chips' were used to quantitatively monitor differential expression of the cognate human genes using a highly sensitive two-color hybridization assay. The identification of known and novel phorbol ester-regulated genes in hematopoietic progenitor cells demonstrates the sensitivity of the assay.     

Products of activated lymphocytes and macrophages inhibit mouse embryo development in vitro

The effects of activated leukocyte products on embryonic development were assessed by adding mouse and human leukocyte culture supernatants and purified murine and human lymphokines and monokines to mouse embryos in tissue culture. Supernatants from mitogen-stimulated and mixed lymphocyte cultures arrested embryonic development at the two-cell to morula stage. Of a panel of six individual lymphokines and monokines tested for effects in this system, both murine and human forms of the lymphokines colony-stimulating factor, interferon-gamma, and human B cell growth factor significantly arrested embryonic development over a wide concentration range. The monokines, interleukin 1 and tumor necrosis factor, also had significant effects but only at high doses. These results indicate that products of activated lymphocytes and macrophages can have detrimental effects on preimplantation embryos. Early abortion could result from local (intrauterine) production of such embryotoxic factors by activated lymphocytes and macrophages in response to stimulation by microorganisms or reproductive tissue antigens.     

An empirical assessment of human development through remote sensing: Evidences from Italy

The Human Development Index (HDI) based on life expectancy, education and per-capita income, is one of the most used indicators of human development. However, undeniable problems in data collection limit between-countries comparisons reducing the practical applicability of the HDI in official statistics. Elvidge et al. (2012) proposed an alternative index of human development (the so called Night Light Development Index, NLDI) derived from nighttime satellite imagery and population density, with improved comparability over time and space. The NLDI assesses inequality in the spatial distribution of night light among resident inhabitants and has proven to correlate with the HDI at the country scale. However, the NLDI presents some drawbacks, since similar NLDI values may indicate very different levels of human development. A modified NLDI overcoming such a drawback is proposed and applied to assessment of human development at 3 spatial scales (the entire country, 5 geographical divisions and 20 administrative regions) in Italy, a country with relevant territorial disparities in various socioeconomic dimensions. The original and modified NLDI were correlated with 5 independent indicators of economic growth, sustainable development and environmental quality. The spatial distribution of the original and modified NLDI is not coherent with the level of human development in Italy being indeed associated with various indexes of environmental quality. Further investigation is required to identify in which socioeconomic context (and at which spatial scale) the NDLI approach correctly estimates the level of human development in affluent countries.