scholarly journals A Regulatory Network for miR156-SPL Module in Arabidopsis thaliana

2019 ◽  
Vol 20 (24) ◽  
pp. 6166 ◽  
Author(s):  
Chenfei Zheng ◽  
Meixia Ye ◽  
Mengmeng Sang ◽  
Rongling Wu
Keyword(s):  
Molecular Mechanisms ◽  
High Throughput Sequencing ◽  
Phase Changes ◽  
Plant Age ◽  
Age Related ◽  
Complex Process ◽  
Spl Genes ◽  
Regulation Network ◽  
Rich Data ◽  
Insight Into

Vegetative phase changes in plants describes the transition between juvenile and adult phases of vegetative growth before flowering. It is one of the most fundamental mechanisms for plants to sense developmental signals, presenting a complex process involving many still-unknown determinants. Several studies in annual and perennial plants have identified the conservative roles of miR156 and its targets, SBP/SPL genes, in guiding the switch of plant growth from juvenile to adult phases. Here, we review recent progress in understanding the regulation of miR156 expression and how miR156-SPLs mediated plant age affect other processes in Arabidopsis. Powerful high-throughput sequencing techniques have provided rich data to systematically study the regulatory mechanisms of miR156 regulation network. From this data, we draw an expanded miR156-regulated network that links plant developmental transition and other fundamental biological processes, gaining novel and broad insight into the molecular mechanisms of plant-age-related processes in Arabidopsis.

scholarly journals MECHANISMS OF BRAIN REJUVENATION

2019 ◽  
Vol 3 (Supplement_1) ◽  
pp. S587-S587
Author(s):  
Saul Villeda
Keyword(s):  
Molecular Mechanisms ◽  
Aging Brain ◽  
Aging Effects ◽  
Effective Strategies ◽  
Mechanistic Insight ◽  
Age Related ◽  
Age Dependent ◽  
Cognitive Faculties ◽  
Insight Into ◽  
Aging Factors

Abstract A growing body of work has shown that systemic manipulations, such as heterochronic parabiosis and young blood administration, can partially reverse age-related cellular impairments and loss of cognitive faculties in the aged brain. These studies have revealed an age-dependent bi-directionality in the influence of the systemic environment indicating anti-aging factors in young blood elicit rejuvenation while pro-aging factors in old blood drive aging. It has been proposed that introducing anti-aging factors or mitigating the effect of pro-aging factors may provide effective strategies to rejuvenate aging phenotypes. Despite this potential, much is unknown as to the systemic and molecular mechanisms regulating anti-aging and pro-aging effects of blood-borne factors. I will discuss work from my research group that begins to provide mechanistic insight into the systemic and molecular drivers promoting rejuvenation in the aging brain.

Defects in cytochrome oxidase assembly in humans: lessons from yeastThis paper is one of a selection of papers published in this Special Issue, entitled CSBMCB — Membrane Proteins in Health and Disease.

2006 ◽  
Vol 84 (6) ◽  
pp. 859-869 ◽  
Author(s):  
Jennifer M. Zee ◽  
D. Moira Glerum
Keyword(s):  
Molecular Mechanisms ◽  
Inner Mitochondrial Membrane ◽  
Yeast Saccharomyces Cerevisiae ◽  
Assembly Pathway ◽  
Complex Process ◽  
Health And Disease ◽  
Molecular Bases ◽  
Near Future ◽  
Insight Into ◽  
Selection Of

The biogenesis of the inner mitochondrial membrane enzyme cytochrome c oxidase (COX) is a complex process that requires the actions of ancillary proteins, collectively called assembly factors. Studies with the yeast Saccharomyces cerevisiae have provided considerable insight into the COX assembly pathway and have proven to be a fruitful model for understanding the molecular bases for inherited COX deficiencies in humans. In this review, we focus on critical steps in the COX assembly pathway. These processes are conserved from yeast to humans and are known to be involved in the etiology of human COX deficiencies. The contributions from our studies in yeast suggest that this organism remains an excellent model system for delineating the molecular mechanisms underlying COX assembly defects in humans. Current progress suggests that a complete picture of COX assembly will be achieved in the near future.

scholarly journals Role of NF-κB in Ageing and Age-Related Diseases: Lessons from Genetically Modified Mouse Models

Cells ◽  
2021 ◽  
Vol 10 (8) ◽  
pp. 1906
Author(s):  
Verónica A. García-García ◽  
Josefa P. Alameda ◽  
Angustias Page ◽  
María Llanos Casanova
Keyword(s):  
Transcription Factor ◽  
Mouse Models ◽  
Molecular Mechanisms ◽  
Inflammatory Responses ◽  
Relevant Information ◽  
Major Mechanism ◽  
Age Related ◽  
Complex Process ◽  
Aged State ◽  
Relationship Of

Ageing is a complex process, induced by multifaceted interaction of genetic, epigenetic, and environmental factors. It is manifested by a decline in the physiological functions of organisms and associated to the development of age-related chronic diseases and cancer development. It is considered that ageing follows a strictly-regulated program, in which some signaling pathways critically contribute to the establishment and maintenance of the aged state. Chronic inflammation is a major mechanism that promotes the biological ageing process and comorbidity, with the transcription factor NF-κB (nuclear factor kappa-light-chain-enhancer of activated B cells) as a crucial mediator of inflammatory responses. This, together with the finding that the activation or inhibition of NF-κB can induce or reverse respectively the main features of aged organisms, has brought it under consideration as a key transcription factor that acts as a driver of ageing. In this review, we focused on the data obtained entirely through the generation of knockout and transgenic mouse models of either protein involved in the NF-κB signaling pathway that have provided relevant information about the intricate processes or molecular mechanisms that control ageing. We have reviewed the relationship of NF-κB and premature ageing; the development of cancer associated with ageing and the implication of NF-κB activation in the development of age-related diseases, some of which greatly increase the risk of developing cancer.

scholarly journals On the chromatin of the immature oocyte: from morphology to function and regulatory mechanisms mediated by follicular cells

2015 ◽  
Author(s):  
Valentina Lodde ◽  
Silvia C. Modina ◽  
Alberto M. Luciano
Keyword(s):  
Cell Biology ◽  
Molecular Mechanisms ◽  
Functional Aspects ◽  
Complex Process ◽  
Chromatin Configuration ◽  
Oocyte Differentiation ◽  
The Relationship ◽  
Insight Into ◽  
Tremendous Impact

In her comment entitled ‘Nuclear histochemistry: its history in fifty volumes’ (Eur J Histochem 2006; 50:79-81) Maria Gabriella Manfredi Romanini referred to “nuclear histochemistry” as a “real molecular biology in situ, applied to research on dynamic processes in the nucleus, which makes the microscopic and histochemical approach absolutely irreplaceable for the progress of our understanding of cell biology”. These words perfectly exemplify the research path that is elucidating the process of remodeling of chromatin configuration within the nucleus of the mammalian oocyte. This process, which occurs towards the end of the oocyte differentiation phase before meiotic resumption, has received much attention in the last decade since it has a tremendous impact on the capability of the oocyte to generate an embryo after fertilization. The study of the oocyte chromatin by means of classical morphological and histochemical approaches has given a fundamental contribution to our understanding of oocyte biology and has paved the way to functional and mechanistic studies. Several research groups worldwide, including ours, are indeed dedicating a large amount of studies to find the relationship between morphological and functional aspects of the oocyte chromatin remodeling process, to reveal the molecular mechanisms involved, as well as to clarify the contribution of the follicular compartment. Here, we summarize some studies intended to give insight into the mechanism( s) regulating this complex process, including recent findings indicating that ovarian granulosa cells and their coupling with the oocyte through gap junctions are implicated in such a process.

scholarly journals Comparative Proteomic Analysis of Young and Adult Bull (Bos taurus) Cryopreserved Semen

Animals ◽  
2021 ◽  
Vol 11 (7) ◽  
pp. 2013
Author(s):  
Błażej Westfalewicz ◽  
Mariola Słowińska ◽  
Sylwia Judycka ◽  
Andrzej Ciereszko ◽  
Mariola A. Dietrich
Keyword(s):  
Proteomic Analysis ◽  
Molecular Mechanisms ◽  
Bos Taurus ◽  
Semen Quality ◽  
Age Related ◽  
Cryopreserved Sperm ◽  
Casa System ◽  
Insight Into ◽  
Sperm Movement

The age of the bull is widely accepted to influence the production of sperm, affecting the amount and quality of produced semen, which in turn impacts the results of cryopreservation. However, the exact influence of the maturation process on cryopreserved sperm, as well as the underlying molecular mechanisms of this process, are not fully understood. The goal of this study was to evaluate changes in the proteome of thawed semen (spermatozoa and supernatant) collected from young and adult bulls (n = 6) using the 2D-DIGE approach. The quality of semen was assessed using a CASA system and flow cytometry. We found no significant age-related variation in semen quality, with the exception of the average path velocity of sperm movement, which was higher in adult bulls. Proteomic analysis indicated 15 spermatozoa proteins and 10 supernatant proteins with significant age-related changes. Our results suggest that semen from adult bulls is better equipped with proteins related to energy production, protection of spermatozoa against oxidative stress and fertilizing ability. Proteins increased in abundance in young bull spermatozoa were connected to the cytoskeleton and its development, which strongly suggests that developmental processes are still in progress. In conclusion, our results provide novel insight into the mechanism of the development of the male reproductive system of cattle.

scholarly journals Age-related increase in matrix stiffness downregulates α-Klotho in chondrocytes and induces cartilage degeneration

2021 ◽  
Author(s):  
Hirotaka Iijima ◽  
Gabrielle Gilmer ◽  
Kai Wang ◽  
Allison Bean ◽  
Yuchen He ◽  
...  
Keyword(s):  
Molecular Mechanisms ◽  
Cartilage Degeneration ◽  
Akt Signaling ◽  
Cartilage Tissue ◽  
Matrix Stiffness ◽  
Knee Cartilage ◽  
Human Knee ◽  
Age Related ◽  
Insight Into ◽  
Upstream Regulators

ABSTRACTEnhanced mechanistic insight into age-related knee osteoarthritis (KOA) is an essential step to promote successful translation of animal research to bedside interventions. To this end, the goal of these studies was to interrogate molecular mechanisms driving age-related KOA in a mouse model and correspond findings to human knee cartilage. Unbiased mass spectrometry proteomics of cartilage tissue revealed PI3K/Akt signaling was the predominant pathway disrupted over time in male, but not female, mice. This finding was consistent with a significantly accelerated KOA progression in males when compared to female counterparts. In probing for upstream regulators of these age-dependent alterations, we found that α-Klotho, a suppressor of PI3K/Akt signaling and potent longevity protein, significantly decreased with aging in both mouse and human knee cartilage. Upstream of these alterations, we found that age-related increases in matrix stiffness initiated a cascade of altered nuclear morphology and downregulated α-Klotho expression, ultimately impairing chondrocyte health. Conversely, reducing matrix stiffness increased α-Klotho expression in chondrocytes, thus enhancing their chondrogencity and cartilage integrity. Collectively, our findings establish a novel mechanistic link between age-related alterations in ECM biophysical properties and regulation of cartilage health by α-Klotho.

scholarly journals SYSTEMIC MECHANISMS OF BRAIN REJUVENATION

2021 ◽  
Vol 5 (Supplement_1) ◽  
pp. 198-198
Author(s):  
Saul Villeda
Keyword(s):  
Molecular Mechanisms ◽  
Circulatory System ◽  
Adult Brain ◽  
Aging Brain ◽  
Aging Effects ◽  
Mechanistic Insight ◽  
Age Related ◽  
The Brain ◽  
Insight Into ◽  
Aging Factors

Abstract Aging drives cellular and cognitive impairments in the adult brain. It is imperative to gain mechanistic insight into what drives aging phenotypes in the brain in order to maintain, and even restore, functional integrity in the elderly. We, and others, have shown that systemic manipulations - such as heterochronic parabiosis (in which a young and old circulatory system are joined) and administration of young blood or exercise induced blood factors - can reverse age-related impairments in regenerative, synaptic and inflammatory processes, as well as rescue cognitive faculties in the aged brain. These studies have revealed an age-dependent bi-directionality in the influence of the systemic environment indicating pro-youthful factors in young blood elicit rejuvenation while pro-aging factors in old blood drive aging. It has been proposed that introducing pro-youthful factors or mitigating the effect of pro-aging factors may provide effective strategies to rejuvenate aging phenotypes in the brain. Despite this potential, much is unknown as to the systemic and molecular mechanisms regulating pro-youthful and pro-aging effects of blood-borne factors. I will discuss work from my research group that begins to provide mechanistic insight into the systemic and molecular drivers promoting rejuvenation in the aging brain.

The Role of Vascular Aging in Atherosclerotic Plaque Development and Vulnerability

2019 ◽  
Vol 25 (29) ◽  
pp. 3098-3111 ◽  
Author(s):  
Luca Liberale ◽  
Giovanni G. Camici
Keyword(s):  
Atherosclerotic Plaque ◽  
Molecular Mechanisms ◽  
Driving Forces ◽  
Plaque Burden ◽  
Vascular Aging ◽  
Age Related ◽  
Plaque Development ◽  
Increased Risk ◽  
The Impact ◽  
Over Time

Background: The ongoing demographical shift is leading to an unprecedented aging of the population. As a consequence, the prevalence of age-related diseases, such as atherosclerosis and its thrombotic complications is set to increase in the near future. Endothelial dysfunction and vascular stiffening characterize arterial aging and set the stage for the development of cardiovascular diseases. Atherosclerotic plaques evolve over time, the extent to which these changes might affect their stability and predispose to sudden complications remains to be determined. Recent advances in imaging technology will allow for longitudinal prospective studies following the progression of plaque burden aimed at better characterizing changes over time associated with plaque stability or rupture. Oxidative stress and inflammation, firmly established driving forces of age-related CV dysfunction, also play an important role in atherosclerotic plaque destabilization and rupture. Several genes involved in lifespan determination are known regulator of redox cellular balance and pre-clinical evidence underlines their pathophysiological roles in age-related cardiovascular dysfunction and atherosclerosis. Objective: The aim of this narrative review is to examine the impact of aging on arterial function and atherosclerotic plaque development. Furthermore, we report how molecular mechanisms of vascular aging might regulate age-related plaque modifications and how this may help to identify novel therapeutic targets to attenuate the increased risk of CV disease in elderly people.

Molecular Mechanisms of Complement System Proteins and Matrix Metalloproteinases in the Pathogenesis of Age-Related Macular Degeneration

2019 ◽  
Vol 19 (10) ◽  
pp. 705-718 ◽  
Author(s):  
Naima Mansoor ◽  
Fazli Wahid ◽  
Maleeha Azam ◽  
Khadim Shah ◽  
Anneke I. den Hollander ◽  
...  
Keyword(s):  
Matrix Metalloproteinases ◽  
Macular Degeneration ◽  
Complement System ◽  
Molecular Mechanisms ◽  
Critical Role ◽  
Age Related Macular Degeneration ◽  
Genetic Changes ◽  
Complement System Proteins ◽  
Age Related ◽  
Common Genetic Variants

: Age-related macular degeneration (AMD) is an eye disorder affecting predominantly the older people above the age of 50 years in which the macular region of the retina deteriorates, resulting in the loss of central vision. The key factors associated with the pathogenesis of AMD are age, smoking, dietary, and genetic risk factors. There are few associated and plausible genes involved in AMD pathogenesis. Common genetic variants (with a minor allele frequency of >5% in the population) near the complement genes explain 40–60% of the heritability of AMD. The complement system is a group of proteins that work together to destroy foreign invaders, trigger inflammation, and remove debris from cells and tissues. Genetic changes in and around several complement system genes, including the CFH, contribute to the formation of drusen and progression of AMD. Similarly, Matrix metalloproteinases (MMPs) that are normally involved in tissue remodeling also play a critical role in the pathogenesis of AMD. MMPs are involved in the degradation of cell debris and lipid deposits beneath retina but with age their functions get affected and result in the drusen formation, succeeding to macular degeneration. In this review, AMD pathology, existing knowledge about the normal and pathological role of complement system proteins and MMPs in the eye is reviewed. The scattered data of complement system proteins, MMPs, drusenogenesis, and lipofusogenesis have been gathered and discussed in detail. This might add new dimensions to the understanding of molecular mechanisms of AMD pathophysiology and might help in finding new therapeutic options for AMD.

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