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      Transcriptomic sex differences in sensory neuronal populations of mice

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          Abstract

          Many chronic pain conditions show sex differences in their epidemiology. This could be attributed to sex-dependent differential expression of genes (DEGs) involved in nociceptive pathways, including sensory neurons. This study aimed to identify sex-dependent DEGs in estrous female versus male sensory neurons, which were prepared by using different approaches and ganglion types. RNA-seq on non-purified sensory neuronal preparations, such as whole dorsal root ganglion (DRG) and hindpaw tissues, revealed only a few sex-dependent DEGs. Sensory neuron purification increased numbers of sex-dependent DEGs. These DEG sets were substantially influenced by preparation approaches and ganglion types [DRG vs trigeminal ganglia (TG)]. Percoll-gradient enriched DRG and TG neuronal fractions produced distinct sex-dependent DEG groups. We next isolated a subset of sensory neurons by sorting DRG neurons back-labeled from paw and thigh muscle. These neurons have a unique sex-dependent DEG set, yet there is similarity in biological processes linked to these different groups of sex-dependent DEGs. Female-predominant DEGs in sensory neurons relate to inflammatory, synaptic transmission and extracellular matrix reorganization processes that could exacerbate neuro-inflammation severity, especially in TG. Male-selective DEGs were linked to oxidative phosphorylation and protein/molecule metabolism and production. Our findings catalog preparation-dependent sex differences in neuronal gene expressions in sensory ganglia.

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          Different immune cells mediate mechanical pain hypersensitivity in male and female mice.

          A large and rapidly increasing body of evidence indicates that microglia-to-neuron signaling is essential for chronic pain hypersensitivity. Using multiple approaches, we found that microglia are not required for mechanical pain hypersensitivity in female mice; female mice achieved similar levels of pain hypersensitivity using adaptive immune cells, likely T lymphocytes. This sexual dimorphism suggests that male mice cannot be used as proxies for females in pain research.
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            Assessing reproductive status/stages in mice.

            The short reproductive cycle length observed in rodents, called the estrous cycle, makes them an ideal animal model for investigation of changes that occur during the reproductive cycle. Most of the data in the literature about the estrous cycle is obtained from rats because they are easily manipulated and they exhibit a clear and well-defined estrous cycle. However, the increased number of experiments using knockout mice requires identification of their estrous cycle as well, since (in)fertility issues may arise. In mice, like rats, the identification of the stage of estrous cycle is based on the proportion of cell types observed in the vaginal secretion. The aim of this unit is to provide guidelines for quickly and accurately determining estrous cycle phases in mice. Copyright 2009 by John Wiley & Sons, Inc.
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              Pain and immunity: implications for host defence

              Pain is a hallmark of tissue injury, inflammatory diseases, pathogen invasion and neuropathy. It is mediated by nociceptor sensory neurons that innervate the skin, joints, bones, muscles and mucosal tissues and protects organisms from noxious stimuli. Nociceptors are sensitized by inflammatory mediators produced by the immune system, including cytokines, lipid mediators and growth factors, and can also directly detect pathogens and their secreted products to produce pain during infection. Upon activation, nociceptors release neuropeptides from their terminals that potently shape the function of innate and adaptive immune cells. For some pathogens, neuron–immune interactions enhance host protection from infection, but for other pathogens neuron–immune signalling pathways can be exploited to facilitate pathogen survival. Here, we discuss the role of nociceptor interactions with the immune system in pain and infection and how understanding these pathways could produce new approaches to treat infectious diseases and chronic pain.
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                Author and article information

                Contributors
                Akopian@UTHSCSA.edu
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                17 September 2020
                17 September 2020
                2020
                : 10
                : 15278
                Affiliations
                [1 ]GRID grid.267309.9, ISNI 0000 0001 0629 5880, Department of Endodontics, , University of Texas Health Science Center at San Antonio (UTHSCSA), ; San Antonio, TX 78229 USA
                [2 ]GRID grid.267309.9, ISNI 0000 0001 0629 5880, Greehey Children’s Cancer Research Institute, , UTHSCSA, ; San Antonio, TX USA
                [3 ]GRID grid.267309.9, ISNI 0000 0001 0629 5880, Department of Molecular Medicine, , University of Texas Health Science Center at San Antonio (UTHSCSA), ; San Antonio, TX 78229 USA
                [4 ]GRID grid.267323.1, ISNI 0000 0001 2151 7939, Department of Neuroscience and Center for Advanced Pain Studies, , University of Texas at Dallas School of Behavioral and Brain Sciences, ; Richardson, TX 75080 USA
                [5 ]GRID grid.267309.9, ISNI 0000 0001 0629 5880, Departments of Microbiology, Immunology & Molecular Genetics, , University of Texas Health Science Center at San Antonio (UTHSCSA), ; San Antonio, TX 78229 USA
                [6 ]GRID grid.267309.9, ISNI 0000 0001 0629 5880, Department of Pharmacology, The School of Dentistry, , University of Texas Health Science Center at San Antonio (UTHSCSA), ; 7703 Floyd Curl Drive, San Antonio, TX 78229-3900 USA
                Author information
                http://orcid.org/0000-0002-6971-6221
                Article
                72285
                10.1038/s41598-020-72285-z
                7499251
                32943709
                8ed675c6-2804-43f1-8b11-3b23b2e13cec
                © The Author(s) 2020

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 29 August 2019
                : 24 August 2020
                Funding
                Funded by: FundRef 100000057, U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS);
                Award ID: S10OD021805
                Award ID: DE029187
                Award Recipient :
                Funded by: FundRef 100000072, U.S. Department of Health & Human Services | NIH | National Institute of Dental and Craniofacial Research (NIDCR);
                Award ID: DE029187
                Funded by: FundRef 100000065, U.S. Department of Health & Human Services | NIH | National Institute of Neurological Disorders and Stroke (NINDS);
                Award ID: NS112263
                Award ID: NS104200
                Award ID: NS102161
                Award ID: NS065926
                Award ID: NS112263
                Award Recipient :
                Funded by: University of Texas at Austin (UT Austin)
                Award ID: 1503083
                Award Recipient :
                Categories
                Article
                Custom metadata
                © The Author(s) 2020

                Uncategorized
                sensory processing,sexual dimorphism,pain
                Uncategorized
                sensory processing, sexual dimorphism, pain

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