OrganogenesisPub Date : 2016-04-02Epub Date: 2016-04-14DOI: 10.1080/15476278.2016.1172164
Sushil Bhandari, Joon No Lee, Young-Il Kim, In-Koo Nam, Su-Jung Kim, Se-Jin Kim, SeongAe Kwak, Gi-Su Oh, Hyung-Jin Kim, Hyun Ju Yoo, Hong-Seob So, Seong-Kyu Choe, Raekil Park
{"title":"The fatty acid chain elongase, Elovl1, is required for kidney and swim bladder development during zebrafish embryogenesis.","authors":"Sushil Bhandari, Joon No Lee, Young-Il Kim, In-Koo Nam, Su-Jung Kim, Se-Jin Kim, SeongAe Kwak, Gi-Su Oh, Hyung-Jin Kim, Hyun Ju Yoo, Hong-Seob So, Seong-Kyu Choe, Raekil Park","doi":"10.1080/15476278.2016.1172164","DOIUrl":"https://doi.org/10.1080/15476278.2016.1172164","url":null,"abstract":"<p><p>Very long chain fatty acids are required for sphingolipid synthesis, lipid homeostasis, myelin formation, epidermal permeability, and retinal function. Seven different enzymes are known to be involved in the elongation cycle of fatty acids, with different chain-length specificities. Elovl1 is one of those enzymes whose function has been linked mainly to the synthesis of sphingolipids and the epidermal barrier. However, the role of Elovl1 in organogenesis is not clear. In zebrafish, 2 Elovl1 genes, elovl1a and elovl1b, are highly expressed in the swim bladder, and elovl1b is also expressed in the kidney. We found that both elovl1 knockdown embryos contain increased levels of long chain fatty acids from carbon number 14 to 20 as compared to control embryos. Oil-Red-O staining shows that yolk lipid consumption is greatly reduced, whereas lipid droplets accumulate within the swim bladder. Notably, knockdown of either elovl1a or elovl1b affects the expression of genes involved in swim bladder development and impairs inflation of the swim bladder. Consistent with its expression in the pronephros, knockdown of elovl1b alone affects the expression of genes required for kidney development and reduces renal clearance. Our findings strongly suggest that both elovl1 genes are a key determinant of swim bladder and kidney development in zebrafish, which may be comparatively applicable to lung and kidney development in humans.</p>","PeriodicalId":19596,"journal":{"name":"Organogenesis","volume":"12 2","pages":"78-93"},"PeriodicalIF":2.3,"publicationDate":"2016-04-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/15476278.2016.1172164","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"34403579","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
OrganogenesisPub Date : 2016-04-02Epub Date: 2016-04-26DOI: 10.1080/15476278.2016.1181238
A Asmar, R Barrett-Jolley, A Werner, R Kelly, M Stacey
{"title":"Membrane channel gene expression in human costal and articular chondrocytes.","authors":"A Asmar, R Barrett-Jolley, A Werner, R Kelly, M Stacey","doi":"10.1080/15476278.2016.1181238","DOIUrl":"https://doi.org/10.1080/15476278.2016.1181238","url":null,"abstract":"<p><p>Chondrocytes are the uniquely resident cells found in all types of cartilage and key to their function is the ability to respond to mechanical loads with changes of metabolic activity. This mechanotransduction property is, in part, mediated through the activity of a range of expressed transmembrane channels; ion channels, gap junction proteins, and porins. Appropriate expression of ion channels has been shown essential for production of extracellular matrix and differential expression of transmembrane channels is correlated to musculoskeletal diseases such as osteoarthritis and Albers-Schönberg. In this study we analyzed the consistency of gene expression between channelomes of chondrocytes from human articular and costal (teenage and fetal origin) cartilages. Notably, we found 14 ion channel genes commonly expressed between articular and both types of costal cartilage chondrocytes. There were several other ion channel genes expressed only in articular (6 genes) or costal chondrocytes (5 genes). Significant differences in expression of BEST1 and KCNJ2 (Kir2.1) were observed between fetal and teenage costal cartilage. Interestingly, the large Ca(2+) activated potassium channel (BKα, or KCNMA1) was very highly expressed in all chondrocytes examined. Expression of the gap junction genes for Panx1, GJA1 (Cx43) and GJC1 (Cx45) was also observed in chondrocytes from all cartilage samples. Together, this data highlights similarities between chondrocyte membrane channel gene expressions in cells derived from different anatomical sites, and may imply that common electrophysiological signaling pathways underlie cellular control. The high expression of a range of mechanically and metabolically sensitive membrane channels suggest that chondrocyte mechanotransduction may be more complex than previously thought.</p>","PeriodicalId":19596,"journal":{"name":"Organogenesis","volume":"12 2","pages":"94-107"},"PeriodicalIF":2.3,"publicationDate":"2016-04-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/15476278.2016.1181238","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"34433890","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
OrganogenesisPub Date : 2016-01-02DOI: 10.1080/15476278.2016.1145317
Z. Makiyan
{"title":"New theory of uterovaginal embryogenesis","authors":"Z. Makiyan","doi":"10.1080/15476278.2016.1145317","DOIUrl":"https://doi.org/10.1080/15476278.2016.1145317","url":null,"abstract":"ABSTRACT Background: The explanation of uterine and vaginal embryogenesis in humans still poses many controversies, because it is difficult to assess early stages of an embryo. The literature review revealed many disagreements in Mullerian theory, inciting some authors to propose new embryological hypotheses. In the original Mullerian theory: the paramesonephral ducts form the Fallopian tubes, uterus and vagina; the mesonephral ducts regress in female embryos. Aims: The aim of this article is to investigate the development of Mullerian ducts in humans, using comparative analysis of fundamental embryological theory and various utero-vaginal anomalies. Material and methods: Between 1998 and 2015, 434 patients with various uterovaginal malformations had been operated on at the Scientific Centre of Obstetrics Gynaecology and Perynatology in Moscow. The anatomies of the uterovaginal malformations in these patients were diagnosed with ultrasound and MRI and then verified during surgical correction by laparoscopy. Results: A systematic comparison of uterovaginal malformations to those in the literature has allowed us to formulate a new theory of embryonic morphogenesis. The new theory is significantly different: ovary, ovarian ligamentum proprium, and ligamentum teres uteri derive from gonadal ridges; Fallopian tubes and vagina completely develop from mesonephral ducts. The uterus develops in the area of intersection between the mesonephral ducts with gonadal ridges by the fusion of the two. Conclusions: The new theory may to induce future embryological studies. The hypothetic possibility that the ovary and endometrium derive from the gonadal ridges could be the key to understanding the enigmatic aetiologies of extragenital and ovarian endometriosis.","PeriodicalId":19596,"journal":{"name":"Organogenesis","volume":"12 1","pages":"33 - 41"},"PeriodicalIF":2.3,"publicationDate":"2016-01-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/15476278.2016.1145317","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"59981933","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
OrganogenesisPub Date : 2016-01-02DOI: 10.1080/15476278.2016.1140290
Julie Bejoy, Liqing Song, Yan Li
{"title":"Wnt-YAP interactions in the neural fate of human pluripotent stem cells and the implications for neural organoid formation","authors":"Julie Bejoy, Liqing Song, Yan Li","doi":"10.1080/15476278.2016.1140290","DOIUrl":"https://doi.org/10.1080/15476278.2016.1140290","url":null,"abstract":"ABSTRACT Human pluripotent stem cells (hPSCs) have shown the ability to self-organize into different types of neural organoids (e.g., whole brain organoids, cortical spheroids, midbrain organoids etc.) recently. The extrinsic and intrinsic signaling elicited by Wnt pathway, Hippo/Yes-associated protein (YAP) pathway, and extracellular microenvironment plays a critical role in brain tissue morphogenesis. This article highlights recent advances in neural tissue patterning from hPSCs, in particular the role of Wnt pathway and YAP activity in this process. Understanding the Wnt-YAP interactions should provide us the guidance to predict and modulate brain-like tissue structure through the regulation of extracellular microenvironment of hPSCs.","PeriodicalId":19596,"journal":{"name":"Organogenesis","volume":"122 1","pages":"1 - 15"},"PeriodicalIF":2.3,"publicationDate":"2016-01-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/15476278.2016.1140290","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"59981897","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
OrganogenesisPub Date : 2016-01-02DOI: 10.1080/15476278.2016.1165378
A. del Toro-Arreola, A. K. Robles-Murillo, A. Daneri-Navarro, J. Rivas-Carrillo
{"title":"The role of endothelial cells on islet function and revascularization after islet transplantation","authors":"A. del Toro-Arreola, A. K. Robles-Murillo, A. Daneri-Navarro, J. Rivas-Carrillo","doi":"10.1080/15476278.2016.1165378","DOIUrl":"https://doi.org/10.1080/15476278.2016.1165378","url":null,"abstract":"ABSTRACT Islet transplantation has become a widely accepted therapeutic option for selected patients with type 1 diabetes mellitus. However, in order to achieve insulin independence a great number of islets are often pooled from 2 to 4 pancreata donors. Mostly, it is due to the massive loss of islets immediately after transplant. The endothelium plays a key role in the function of native islets and during the revascularization process after islet transplantation. However, if a delayed revascularization occurs, even the remaining islets will also undergo to cell death and late graft dysfunction. Therefore, it is essential to understand how the signals are released from endothelial cells, which might regulate both differentiation of pancreatic progenitors and thereby maintenance of the graft function. New strategies to facilitate islet engraftment and a prompt revascularization could be designed to intervene and might lead to improve future results of islet transplantation.","PeriodicalId":19596,"journal":{"name":"Organogenesis","volume":"35 1","pages":"28 - 32"},"PeriodicalIF":2.3,"publicationDate":"2016-01-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/15476278.2016.1165378","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"59981975","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
OrganogenesisPub Date : 2016-01-02DOI: 10.1080/15476278.2016.1145318
Z. Makiyan
{"title":"Studies of gonadal sex differentiation","authors":"Z. Makiyan","doi":"10.1080/15476278.2016.1145318","DOIUrl":"https://doi.org/10.1080/15476278.2016.1145318","url":null,"abstract":"ABSTRACT Gonadal differentiation has a determinative influence on sex development in human embryos. Disorders of sexual development (DSD) have been associated with persistent embryonal differentiation stages. Between 1998 and 2015, 139 female patients with various (DSD) underwent operations at the Scientific Center of Obstetrics, Gynaecology and Perynatology in Moscow, Russia. Clinical investigations included karyotyping, ultrasound imaging, hormonal measurement and investigations of gonadal morphology. The male characteristics in the embryo are imposed by testicular hormones. When these are absent or inactive, the fetus may be arrested at between developmental stages, or stay on indifferent stage and become phenotypically female. A systematic analysis of gonadal morphology in DSD patients and a literature review revealed some controversies and led us to formulate a new hypothesis about sex differentiation. Proliferation of the mesonephric system (tubules and corpuscles) in the gonads stimulates the masculinization of gonads to testis. Sustentacular Sertoli cells of the testes are derived from mesonephric excretory tubules, while interstitial Leydig cells are derived from the original mesenchyme of the mesonephros. According of the new hypothesis, the original mesonephric cells (tubules and corpuscles) potentially persist in the ovarian parenchyma. In female gonads, some mesonephric excretory tubules regress and lose the tubular structure, but form ovarian theca interna and externa, becoming analogous to the sustentacular Sertoli cells in the testis. The ovarian interstitial Leydig cells are derived from intertubal mesenchyme of the mesonephros, similar to what occurs in male gonads (testis). Surprisingly, the leading determinative factor in sexual differentiation of the gonads is the mesonephros, represented by the embryonic urinary system.","PeriodicalId":19596,"journal":{"name":"Organogenesis","volume":"8 12 1","pages":"42 - 51"},"PeriodicalIF":2.3,"publicationDate":"2016-01-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/15476278.2016.1145318","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"59981964","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
OrganogenesisPub Date : 2016-01-02DOI: 10.1080/15476278.2016.1163463
Elizabeth R. Zielins, R. C. Ransom, Tripp Leavitt, M. Longaker, D. Wan
{"title":"The role of stem cells in limb regeneration","authors":"Elizabeth R. Zielins, R. C. Ransom, Tripp Leavitt, M. Longaker, D. Wan","doi":"10.1080/15476278.2016.1163463","DOIUrl":"https://doi.org/10.1080/15476278.2016.1163463","url":null,"abstract":"ABSTRACT Limb regeneration is a complex yet fascinating process observed to some extent in many animal species, though seen in its entirety in urodele amphibians. Accomplished by formation of a morphologically uniform intermediate, the blastema, scientists have long attempted to define the cellular constituents that enable regrowth of a functional appendage. Today, we know that the blastema consists of a variety of multipotent progenitor cells originating from a variety of tissues, and which contribute to limb tissue regeneration in a lineage-restricted manner. By continuing to dissect the role of stem cells in limb regeneration, we can hope to one day modulate the human response to limb amputation and facilitate regrowth of a working replacement.","PeriodicalId":19596,"journal":{"name":"Organogenesis","volume":"12 1","pages":"16 - 27"},"PeriodicalIF":2.3,"publicationDate":"2016-01-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/15476278.2016.1163463","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"59981969","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
OrganogenesisPub Date : 2015-10-02DOI: 10.1080/15476278.2015.1120047
Takamasa Tobita, J. Guzman‐Lepe, Alexandra Collin de l'Hortet
{"title":"From hacking the human genome to editing organs","authors":"Takamasa Tobita, J. Guzman‐Lepe, Alexandra Collin de l'Hortet","doi":"10.1080/15476278.2015.1120047","DOIUrl":"https://doi.org/10.1080/15476278.2015.1120047","url":null,"abstract":"ABSTRACT In the recent decades, human genome engineering has been one of the major interesting research subjects, essentially because it raises new possibilities for personalized medicine and biotechnologies. With the development of engineered nucleases such as the Zinc Finger Nucleases (ZFNs), the Transcription activator-like effector nucleases (TALENs) and more recently the Clustered Regularly Interspaced short Palindromic Repeats (CRISPR), the field of human genome edition has evolved very rapidly. Every new genetic tool is broadening the scope of applications on human tissues, even before we can completely master each of these tools. In this review, we will present the recent advances regarding human genome edition tools, we will discuss the numerous implications they have in research and medicine, and we will mention the limits and concerns about such technologies","PeriodicalId":19596,"journal":{"name":"Organogenesis","volume":"11 1","pages":"173 - 182"},"PeriodicalIF":2.3,"publicationDate":"2015-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/15476278.2015.1120047","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"59981884","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
OrganogenesisPub Date : 2015-10-02DOI: 10.1080/15476278.2015.1120046
E. Stahl, B. Brown
{"title":"Cell Therapy Strategies to Combat Immunosenescence","authors":"E. Stahl, B. Brown","doi":"10.1080/15476278.2015.1120046","DOIUrl":"https://doi.org/10.1080/15476278.2015.1120046","url":null,"abstract":"abstract Declining function of the immune system, termed “immunosenescence,” leads to a higher incidence of infection, cancer, and autoimmune disease related mortalities in the elderly population.1 Increasing interest in the field of immunosenescence is well-timed, as 20% of the United States population is expected to surpass the age of 65 by the year 2030.2 Our current understanding of immunosenescence involves a shift in function of both adaptive and innate immune cells, leading to a reduced capacity to recognize new antigens and widespread chronic inflammation. The present review focuses on changes that occur in haematopoietic stem cells, macrophages, and T-cells using knowledge gained from both rodent and human studies. The review will discuss emerging strategies to combat immunosenescence, focusing on cellular and genetic therapies, including bone marrow transplantation and genetic reprogramming. A better understanding of the mechanisms and implications of immunosenescence will be necessary to combat age-related mortalities in the future.","PeriodicalId":19596,"journal":{"name":"Organogenesis","volume":"11 1","pages":"159 - 172"},"PeriodicalIF":2.3,"publicationDate":"2015-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/15476278.2015.1120046","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"59981877","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
OrganogenesisPub Date : 2015-01-01DOI: 10.1080/15476278.2015.1123360
Fu-Yu Hsieh, Shan-hui Hsu
{"title":"3D bioprinting: A new insight into the therapeutic strategy of neural tissue regeneration.","authors":"Fu-Yu Hsieh, Shan-hui Hsu","doi":"10.1080/15476278.2015.1123360","DOIUrl":"10.1080/15476278.2015.1123360","url":null,"abstract":"<p><p>Acute traumatic injuries and chronic degenerative diseases represent the world's largest unmet medical need. There are over 50 million people worldwide suffering from neurodegenerative diseases. However, there are only a few treatment options available for acute traumatic injuries and neurodegenerative diseases. Recently, 3D bioprinting is being applied to regenerative medicine to address the need for tissues and organs suitable for transplantation. In this commentary, the newly developed 3D bioprinting technique involving neural stem cells (NSCs) embedded in the thermoresponsive biodegradable polyurethane (PU) bioink is reviewed. The thermoresponsive and biodegradable PU dispersion can form gel near 37 °C without any crosslinker. NSCs embedded within the water-based PU hydrogel with appropriate stiffness showed comparable viability and differentiation after printing. Moreover, in the zebrafish embryo neural deficit model, injection of the NSC-laden PU hydrogels promoted the repair of damaged CNS. In addition, the function of adult zebrafish with traumatic brain injury was rescued after implantation of the 3D-printed NSC-laden constructs. Therefore, the newly developed 3D bioprinting technique may offer new possibilities for future therapeutic strategy of neural tissue regeneration.</p>","PeriodicalId":19596,"journal":{"name":"Organogenesis","volume":"11 1","pages":"153-8"},"PeriodicalIF":2.3,"publicationDate":"2015-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/15476278.2015.1123360","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"59981889","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}