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  1. Article: Effects of the neuropeptides substance P, calcitonin gene-related peptide, vasoactive intestinal polypeptide and galanin on the production of nerve growth factor and inflammatory cytokines in cultured human keratinocytes.

    Dallos, Attila / Kiss, Mária / Polyánka, Hilda / Dobozy, Attila / Kemény, Lajos / Husz, Sándor

    Neuropeptides

    2006  Volume 40, Issue 4, Page(s) 251–263

    Abstract: ... substance P (SP), calcitonin gene-related peptide (CGRP), vasoactive intestinal polypeptide (VIP) and ...

    Abstract Neuropeptides released from the cutaneous sensory nerve endings have neurotransmitter and immunoregulatory roles; they exert mitogenic actions and can influence the functions of different cell types in the skin. The aims of this study were a systematic investigation of the effects of the neuropeptides substance P (SP), calcitonin gene-related peptide (CGRP), vasoactive intestinal polypeptide (VIP) and galanin (GAL) on the inflammatory cytokine production (IL-1alpha, IL-8 and TNF-alpha) of the keratinocytes, and a study of their role in the production and secretion of nerve growth factor (NGF) and its precursor molecule (proNGF). Cultures of normal human keratinocytes were treated with 10(-8)M SP, CGRP, VIP or GAL for 30 min. After different time intervals, cells were harvested for total RNA isolation; in addition, cell lysates and supernatants were collected. The effects of the neuropeptides on the mRNA expressions of the different cytokines and NGF were investigated by Q-RT-PCR and the protein levels were studied by means of ELISA assays and Western blotting. Each of the four neuropeptides induced increases in the expressions of IL-1alpha, IL-8 and TNF-alpha mRNA. Increases appeared in the amount of the IL-1alpha protein in the supernatants of neuropeptide-treated cells, and the IL-8 secretion was mildly elevated, while secretion of TNF-alpha remained undetectable. The four neuropeptides increased the NGF mRNA expression to different extents. In the cell lysates of the keratinocytes, only proNGF could be detected, its concentration in the neuropeptide-treated cells being approximately twice that in the time-matched controls. Both control cultures and neuropeptide-treated cultures were found to secrete proNGF and mature NGF, but neuropeptide-treated cell cultures produced markedly higher (3-7-fold) amounts of NGF-like immunoreactive materials. The results demonstrated that neuropeptides released from cutaneous nerves after an injurious stimulus are able to induce an upregulation of IL-1alpha and IL-8 production; they are additionally able to influence the expressions of proNGF/NGF and their secretion from the keratinocytes. These findings may contribute toward an understanding of the neural influence on skin health and disease.
    MeSH term(s) Calcitonin Gene-Related Peptide/metabolism ; Cells, Cultured ; Cytokines/genetics ; Cytokines/metabolism ; Female ; Galanin/metabolism ; Humans ; Inflammation/metabolism ; Keratinocytes/cytology ; Keratinocytes/metabolism ; Nerve Growth Factor/metabolism ; Protein Precursors/metabolism ; RNA, Messenger/metabolism ; Substance P/metabolism ; Vasoactive Intestinal Peptide/metabolism
    Chemical Substances Cytokines ; Protein Precursors ; RNA, Messenger ; Substance P (33507-63-0) ; Vasoactive Intestinal Peptide (37221-79-7) ; Calcitonin Gene-Related Peptide (83652-28-2) ; Galanin (88813-36-9) ; Nerve Growth Factor (9061-61-4)
    Language English
    Publishing date 2006-08
    Publishing country Netherlands
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 9048-7
    ISSN 1532-2785 ; 0143-4179
    ISSN (online) 1532-2785
    ISSN 0143-4179
    DOI 10.1016/j.npep.2006.06.002
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: WITHDRAWN: Feedback in the cochlea.

    Dallos, Peter

    Hearing research

    2010  

    Abstract: This article has been withdrawn at the request of the author(s) and/or editor. The Publisher apologizes for any inconvenience this may cause. The full Elsevier Policy on Article Withdrawal can be found at http://www.elsevier.com/locate/withdrawalpolicy. ...

    Abstract This article has been withdrawn at the request of the author(s) and/or editor. The Publisher apologizes for any inconvenience this may cause. The full Elsevier Policy on Article Withdrawal can be found at http://www.elsevier.com/locate/withdrawalpolicy.
    Language English
    Publishing date 2010-01-30
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 282629-x
    ISSN 1878-5891 ; 0378-5955
    ISSN (online) 1878-5891
    ISSN 0378-5955
    DOI 10.1016/j.heares.2009.12.009
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: Case report: Prader-Willi syndrome and inflammatory arthritis-An important consideration.

    Marelli, Luca / Dallos, Tomáš / Miserocchi, Elisabetta / Nucci, Paolo / Tombolini, Beatrice / De Lucia, Orazio / Gattinara, Maurizio / Caporali, Roberto / Marino, Achille

    Frontiers in pediatrics

    2023  Volume 11, Page(s) 1102382

    Abstract: Background: Prader-Willi syndrome (PWS) is a multisystemic genetically determined disorder. Musculoskeletal manifestations are common in most patients. We report the cases of two children with PWS who developed inflammatory arthritis, complicated with ... ...

    Abstract Background: Prader-Willi syndrome (PWS) is a multisystemic genetically determined disorder. Musculoskeletal manifestations are common in most patients. We report the cases of two children with PWS who developed inflammatory arthritis, complicated with chronic anterior bilateral uveitis in one case. To our knowledge, no previous reports of such an association exist.
    Case presentation: Case 1 was of a 3-year-old girl diagnosed with PWS who developed arthritis of the right knee with morning stiffness, joint swelling, and limited range of motion. Other causes of arthritis were ruled out. Increased inflammatory markers, antinuclear antibody (ANA) positivity, and hypertrophic synovitis on ultrasound confirmed the diagnosis of inflammatory arthritis compatible with juvenile idiopathic arthritis (JIA). Despite the treatment with methotrexate, arthritis progressed, and etanercept was added. The patient reached and maintained articular remission while on combined MTX and etanercept treatment during 9 years of follow-up. Case 2 was of a 6-year-old boy diagnosed with PWS who developed arthritis of the right knee. Laboratory investigations showed mildly increased acute phase reactants, microcytic anemia, and ANA positivity at high titer (titer 1:1,280). Infectious and other causes of arthritis were excluded. Ultrasound confirmed the presence of joint effusion and synovial thickening, and synovial fluid analysis was consistent with inflammatory arthrosynovitis (white blood cell count of 14,200/µl) compatible with JIA. Shortly after the diagnosis, the ophthalmologic evaluation revealed the presence of bilateral anterior uveitis. Despite MTX and topical corticosteroid, ocular inflammation persisted and adalimumab was added. At the last follow-up, 9 months later, the child experienced inactivity of arthritis and uveitis with normal growth.
    Conclusions: We aim to raise awareness of this possible association among pediatricians since arthritis might be underestimated due to high pain tolerance, behavioral disturbances, and other musculoskeletal abnormalities in PWS patients.
    Language English
    Publishing date 2023-03-17
    Publishing country Switzerland
    Document type Case Reports
    ZDB-ID 2711999-3
    ISSN 2296-2360
    ISSN 2296-2360
    DOI 10.3389/fped.2023.1102382
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article: Micropropagation of cubio (Tropaeolum tuberosum R & P)

    Torres, O / Perea-Dallos, M / Fandino, T.J

    Biotechnology in agriculture and forestry. 1991. v. 19

    1991  

    Keywords Tropaeolum tuberosum ; agronomic traits ; geographical distribution ; genetic improvement ; in vitro culture ; micropropagation ; culture media ; South America
    Language English
    Size p. 160-171.
    Document type Article
    Note In the series analytic: High-tech and micropropagation III / edited by Y.P.S. Bajaj.
    ZDB-ID 2000537-4
    ISSN 0934-943X
    ISSN 0934-943X
    Database NAL-Catalogue (AGRICOLA)

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  5. Article: Cochlear amplification, outer hair cells and prestin.

    Dallos, Peter

    Current opinion in neurobiology

    2008  Volume 18, Issue 4, Page(s) 370–376

    Abstract: Mechanical amplification of acoustic signals is apparently a common feature of vertebrate auditory organs. In non-mammalian vertebrates amplification is produced by stereociliary processes, related to the mechanotransducer channel complex and probably to ...

    Abstract Mechanical amplification of acoustic signals is apparently a common feature of vertebrate auditory organs. In non-mammalian vertebrates amplification is produced by stereociliary processes, related to the mechanotransducer channel complex and probably to the phenomenon of fast adaptation. The extended frequency range of the mammalian cochlea has probably co-evolved with a novel hair cell type, the outer hair cell and its constituent membrane protein, prestin. Cylindrical outer hair cells are motile and their somatic length changes are voltage driven and powered by prestin. One of the central outstanding problems in mammalian cochlear neurobiology is the relation between the two amplification processes.
    MeSH term(s) Animals ; Anion Transport Proteins/physiology ; Auditory Threshold/physiology ; Cell Movement/physiology ; Cochlea/cytology ; Cochlea/physiology ; Hair Cells, Auditory, Outer/cytology ; Hair Cells, Auditory, Outer/physiology ; Hearing/physiology ; Humans ; Mechanotransduction, Cellular/physiology ; Organ of Corti/cytology ; Organ of Corti/physiology
    Chemical Substances Anion Transport Proteins ; SLC26A5 protein, human
    Language English
    Publishing date 2008-08
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Review
    ZDB-ID 1078046-4
    ISSN 1873-6882 ; 0959-4388
    ISSN (online) 1873-6882
    ISSN 0959-4388
    DOI 10.1016/j.conb.2008.08.016
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Book: The auditory periphery

    Dallos, Peter

    biophysics and physiology

    1973  

    Author's details Peter Dallos
    Keywords Hören ; Physiologie
    Subject Humanphysiologie ; Mensch ; Körperfunktion ; Gehör
    Language English
    Size XII, 548 S.
    Publisher Acad. Press
    Publishing place New York u.a.
    Publishing country United States
    Document type Book
    HBZ-ID HT005174780
    ISBN 0-12-200750-6 ; 978-0-12-200750-7
    Database Catalogue ZB MED Medicine, Health

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  7. Article ; Online: Topochemical Fluorination of LaBaInO

    Perween, Shama / Wissel, Kerstin / Dallos, Zsolt / Weiss, Morten / Ikeda, Yuji / Vasala, Sami / Strobel, Sabine / Schützendübe, Peter / Jeschenko, Pascal M / Kolb, Ute / Marschall, Roland / Grabowski, Blazej / Glatzel, Pieter

    Inorganic chemistry

    2023  Volume 62, Issue 40, Page(s) 16329–16342

    Abstract: We report on a nonoxidative topochemical route for the synthesis of a novel indate-based oxyfluoride, ... ...

    Abstract We report on a nonoxidative topochemical route for the synthesis of a novel indate-based oxyfluoride, LaBaInO
    Language English
    Publishing date 2023-09-27
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1484438-2
    ISSN 1520-510X ; 0020-1669
    ISSN (online) 1520-510X
    ISSN 0020-1669
    DOI 10.1021/acs.inorgchem.3c01682
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article: KLRG1 marks tumor-infiltrating CD4 T cell subsets associated with tumor progression and immunotherapy response.

    Ager, Casey R / Zhang, Mingxuan / Chaimowitz, Matthew / Bansal, Shruti / Obradovic, Aleksandar / Rogava, Meri / Melms, Johannes C / McCann, Patrick / Spina, Catherine / Drake, Charles G / Dallos, Matthew C / Izar, Benjamin

    bioRxiv : the preprint server for biology

    2023  

    Abstract: Current methods for biomarker discovery and target identification in immuno-oncology rely on static snapshots of tumor immunity. To thoroughly characterize the temporal nature of antitumor immune responses, we developed a 34-parameter spectral flow ... ...

    Abstract Current methods for biomarker discovery and target identification in immuno-oncology rely on static snapshots of tumor immunity. To thoroughly characterize the temporal nature of antitumor immune responses, we developed a 34-parameter spectral flow cytometry panel and performed high-throughput analyses in critical contexts. We leveraged two distinct preclinical models that recapitulate cancer immunoediting (NPK-C1) and immune checkpoint blockade (ICB) response (MC38), respectively, and profiled multiple relevant tissues at and around key inflection points of immune surveillance and escape and/or ICB response. Machine learning-driven data analysis revealed a pattern of KLRG1 expression that uniquely identified intratumoral effector CD4 T cell populations that constitutively associate with tumor burden across tumor models, and are lost in tumors undergoing regression in response to ICB. Similarly, a Helios
    Language English
    Publishing date 2023-01-02
    Publishing country United States
    Document type Preprint
    DOI 10.1101/2023.01.01.522340
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: KLRG1 marks tumor-infiltrating CD4 T cell subsets associated with tumor progression and immunotherapy response.

    Ager, Casey R / Zhang, Mingxuan / Chaimowitz, Matthew / Bansal, Shruti / Tagore, Somnath / Obradovic, Aleksandar / Jugler, Collin / Rogava, Meri / Melms, Johannes C / McCann, Patrick / Spina, Catherine / Drake, Charles G / Dallos, Matthew C / Izar, Benjamin

    Journal for immunotherapy of cancer

    2023  Volume 11, Issue 9

    Abstract: Current methods for biomarker discovery and target identification in immuno-oncology rely on static snapshots of tumor immunity. To thoroughly characterize the temporal nature of antitumor immune responses, we developed a 34-parameter spectral flow ... ...

    Abstract Current methods for biomarker discovery and target identification in immuno-oncology rely on static snapshots of tumor immunity. To thoroughly characterize the temporal nature of antitumor immune responses, we developed a 34-parameter spectral flow cytometry panel and performed high-throughput analyses in critical contexts. We leveraged two distinct preclinical models that recapitulate cancer immunoediting (NPK-C1) and immune checkpoint blockade (ICB) response (MC38), respectively, and profiled multiple relevant tissues at and around key inflection points of immune surveillance and escape and/or ICB response. Machine learning-driven data analysis revealed a pattern of KLRG1 expression that uniquely identified intratumoral effector CD4 T cell populations that constitutively associate with tumor burden across tumor models, and are lost in tumors undergoing regression in response to ICB. Similarly, a Helios
    MeSH term(s) Humans ; CD4-Positive T-Lymphocytes ; T-Lymphocyte Subsets ; Carcinoma, Renal Cell ; Kidney Neoplasms ; Immunotherapy ; Biomarkers ; Receptors, Immunologic ; Lectins, C-Type
    Chemical Substances Biomarkers ; KLRG1 protein, human ; Receptors, Immunologic ; Lectins, C-Type
    Language English
    Publishing date 2023-08-30
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, N.I.H., Extramural
    ZDB-ID 2719863-7
    ISSN 2051-1426 ; 2051-1426
    ISSN (online) 2051-1426
    ISSN 2051-1426
    DOI 10.1136/jitc-2023-006782
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Current status of engineered T-cell therapy for synovial sarcoma.

    Dallos, Matthew / Tap, William D / D'Angelo, Sandra P

    Immunotherapy

    2016  Volume 8, Issue 9, Page(s) 1073–1080

    Abstract: Synovial sarcoma is a rare soft tissue sarcoma characterized by a t(X;18) translocation, which results in a SYT-SSX gene fusion. In the metastatic setting, chemotherapy has limited, durable efficacy prompting the necessity for new therapeutic modalities. ...

    Abstract Synovial sarcoma is a rare soft tissue sarcoma characterized by a t(X;18) translocation, which results in a SYT-SSX gene fusion. In the metastatic setting, chemotherapy has limited, durable efficacy prompting the necessity for new therapeutic modalities. One emerging new strategy involves T-cell-directed therapy such as tumor-infiltrating lymphocytes or the development of T cells that are genetically engineered to express a T-cell receptor against a cancer testis antigen. Of these approaches, engineered T cells that recognize NY-ESO-1 are the furthest along in development. Completed and on-going clinical trials have shown promise and there are efforts to continue to optimize the current approach.
    MeSH term(s) Antigens, Neoplasm/immunology ; Chromosomes, Human, Pair 18/genetics ; Clinical Trials as Topic ; Epithelial-Mesenchymal Transition ; Female ; Gene Fusion ; Genetic Engineering ; Humans ; Immunotherapy, Adoptive/methods ; Lymphocytes, Tumor-Infiltrating/physiology ; Lymphocytes, Tumor-Infiltrating/transplantation ; Male ; Membrane Proteins/immunology ; Neoplasm Proteins/genetics ; Proto-Oncogene Proteins/genetics ; Receptors, Antigen, T-Cell/genetics ; Recombinant Fusion Proteins/genetics ; Repressor Proteins/genetics ; Sarcoma, Synovial/genetics ; Sarcoma, Synovial/immunology ; Sarcoma, Synovial/therapy ; T-Lymphocytes/physiology ; T-Lymphocytes/transplantation
    Chemical Substances Antigens, Neoplasm ; CTAG1B protein, human ; Membrane Proteins ; Neoplasm Proteins ; Proto-Oncogene Proteins ; Receptors, Antigen, T-Cell ; Recombinant Fusion Proteins ; Repressor Proteins ; SS18 protein, human ; synovial sarcoma X breakpoint proteins (164289-47-8)
    Language English
    Publishing date 2016
    Publishing country England
    Document type Journal Article ; Review
    ISSN 1750-7448
    ISSN (online) 1750-7448
    DOI 10.2217/imt-2016-0026
    Database MEDical Literature Analysis and Retrieval System OnLINE

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