Cellular and molecular basis of {TNFα [TNF-alpha], {IL-1β [IL-1-beta] and LPS mediated signaling in rat dorsal root ganglion [Elektronische Ressource] / vorgelegt von Yanzhang Li
Aus dem Institut für Anatomie und Zellbiologie der Philipps-Universität Marburg Abteilung Molekulare Neurowissenschaften Direktor: Professor Dr. E. Weihe Cellular and molecular basis of TNFα, IL-1β and LPS mediated signaling in rat dorsal root ganglion Inaugural Dissertation zur Erlangung des Doktorgrades der Humanbiologie (Dr. rer. physiol.) dem Fachbereich Humanmedizin der Philipps-Universität Marburg vorgelegt von Yanzhang Li aus Henan, V. R. China Marburg 2004 Angenommen vom Fachbereich Humanmedizin der Philipps-Universität Marburg am 19.05. 2004 Gedruckt mit Genehmigung des Fachbereichs Dekan: Prof. Dr. Bernhard Maisch Referent: Prof. Dr. Eberhard Weihe Korreferent: Prof. Dr. Michael Lohoff Contents Contents 1. Introduction.............................................................................................. 1 1.1 Role of primary sensory neurons of the dorsal root ganglion.............................. 1 1.2 TNFα in the dorsal root ganglion ........................................................................ 2 1.3 TNF receptor subtypes and their expression in primary sensory neurons of the dorsal root ganglion ....................................................................................... 2 1.4 TNFα and nociception......................................................................................... 3 1.
Aus dem Institut für Anatomie und Zellbiologie der Philipps-Universität Marburg Abteilung Molekulare Neurowissenschaften Direktor: Professor Dr. E. Weihe Cellular and molecular basis of TNFα, IL-1βand LPS
mediated signaling in rat dorsal root ganglion
Inaugural Dissertation zur Erlangung des Doktorgrades der Humanbiologie (Dr. rer. physiol.) dem Fachbereich Humanmedizin der Philipps-Universität Marburg vorgelegt von Yanzhang Li
1.1 Role of primary sensory neurons of the dorsal root ganglion.............................. 1
1.2 TNFαin the dorsal root ganglion ........................................................................ 2
1.3 TNF receptor subtypes and their expression in primary sensory neurons of the dorsal root ganglion ....................................................................................... 2
Materials and Methods ......................................................................... 10
2.1 Materials ............................................................................................................ 10 2.1.1Equipment ........................................................................................................................ 102.1.2 10 ...................................................................................................Chemicals and reagents2.1.3Buffers and solutions........................................................................................................ 122.1.4Cell lines .......................................................................................................................... 152.1.5Animals ............................................................................................................................ 152.1.6Radioactive nucleotides ................................................................................................... 152.1.7Antibodies ........................................................................................................................ 152.1.8 15Kits ...................................................................................................................................2.1.9Enzymes ........................................................................................................................... 162.1.10Oligonucleotides .............................................................................................................. 162.1.11cDNA constructs .............................................................................................................. 182.1.12DNA, RNA and protein size markers ............................................................................... 182.1.13 ..................................................................................................................Other supplies 192.2 Methods.............................................................................................................. 19 2.2.1Animal treatment.............................................................................................................. 192.2.2Cell culture ...................................................................................................................... 192.2.3Laser capture microdissection (LCM) ............................................................................. 202.2.4RNA isolation from tissues and F11 cells ........................................................................ 202.2.5cDNA synthesis ................................................................................................................ 202.2.5.1Synthesis of cDNA for PCR..................................................................................... 202.2.5.2Synthesis of cDNA for RACE................................................................................... 21
I
3
Contents
2.2.6Polymerase chain reaction (PCR) ................................................................................... 212.2.7Rapid amplification of cDNA ends (RACE) of the rat TNFR2 gene ................................ 222.2.8DNA agarose gel electrophoresis .................................................................................... 222.2.9Cloning of PCR products into plasmid vectors................................................................ 222.2.10In vitro transcription........................................................................................................ 232.2.11 23 .........................................................................................................In situ hybridization2.2.11.1Coating of glass slides........................................................................................ 232.2.11.2Preparation of tissue sections............................................................................ 242.2.11.3nioridhaezibytrP................................................................................................... 242.2.11.4ybHdiritizaon......................................................................................................... 242.2.11.5Posthybridization and detection......................................................................... 242.2.12Double in situ hybridization............................................................................................. 252.2.13Northern Blot Analysis..................................................................................................... 262.2.13.1RNA agarose gel electrophoresis..................................................................... 262.2.13.2RNA transfer......................................................................................................... 262.2.13.3Detection of 18S and 28S RNA or RNA markers........................................... 272.2.13.4Hybridization of blot and detection of mRNAs................................................. 272.2.14 27Western blot analysis .......................................................................................................2.2.14.1SDS polyacrylamide gel electrophoresis.......................................................... 272.2.14.2Protein transfer and detection............................................................................ 27Results.....................................................................................................29
3.1 Characterization of the rat TNFR2 gene ............................................................ 29 3.1.1Full length cloning of rat TNFR2 cDNA.......................................................................... 293.1.2Alignment of rat TNFR2 putative amino acids with that of mouse and human................ 293.1.3Structure of the rat TNFR2 gene...................................................................................... 303.1.4Tissue-specific distribution of rat TNFR2 transcripts...................................................... 323.1.5LPS-induced regulation of TNFR2 gene in rat spleen ..................................................... 323.2 Expression of TNF receptors in rat dorsal root ganglion................................... 33 3.2.1RNA extracts of rat dorsal root ganglion .......... 33RT-PCR detection of TNF receptors in 3.2.2Northern blot analysis of TNF receptor expression in rat dorsal root ganglion: effects of LPS ................................................................................................................... 343.2.3RT-PCR analysis of TNF receptor expression in microdissected dorsal root ganglion neurons ............................................................................................................................ 353.2.4TNF receptor expression in the F11 cell line................................................................... 353.2.5Cellular distribution of TNF receptor mRNAs in rat dorsal root ganglion and regulation of their expression after LPS .......................................................................... 363.2.6Relationship of TNFR1 expression with putative nociceptive neurons expressing SP, CGRP or VR1................................................................................................................... 38
II
4
3.3
3.4
Contents
Constitutive and LPS-induced cell-specific expression of TNFαmRNA in
rat dorsal root ganglion ...................................................................................... 38
Expression of IL-1R1 and IL-1β ............................. 40in rat dorsal root ganglion
3.4.1RT-PCR detection of IL-1R1 and IL-1βin RNA extracts of rat dorsal root ganglion ..... 403.4.2RT-PCR analysis of IL-1R1 and IL-1βexpression in microdissected dorsal root ganglion neurons ............................................................................................................. 403.4.3Northern blot analysis of IL-1R1 expression in rat dorsal root ganglion and in the
3.4.43.4.5
3.4.6
F11 cell line ..................................................................................................................... 41
Cell-specific expression of IL-1R1 mRNA in rat dorsal root ganglion ............................ 41
Relationship of IL-1R1 expression with putative nociceptive neuronal populations
expressing SP, CGRP and VR1........................................................................................ 42Constitutive and LPS-induced cellular distribution of IL-1βin rat dorsal root
ganglion ........................................................................................................................... 443.5 Expression of LPS receptors in rat dorsal root ganglion ................................... 45 3.5.1RT-PCR detection of TLR4 and CD14 in RNA extracts of rat dorsal root ganglion ....... 453.5.2Northern blot analysis of TLR4 and CD14 expression in rat dorsal root ganglion......... 453.5.3analysis of TLR4 expression in microdissected dorsal root ganglion neurons . 46RT-PCR 3.5.4Cellular distribution of constitutive TLR4 expression in rat dorsal root ganglion.......... 473.5.5Relationship of TLR4 expression with putative nociceptive neuronal populations expressing SP, CGRP or VR1 .......................................................................................... 483.5.6and LPS-induced cellular distribution of CD14 in rat dorsal rootConstitutive ganglion ........................................................................................................................... 49Discussion ............................................................................................... 51
4.1 Identification, structural characterization, tissue-specific distribution and
LPS-induced regulation of the rat TNFR2 gene ................................................ 51 4.2 Functional implications of TNFR1 and TNFR2 expression in rat dorsal root ganglion.............................................................................................................. 53 4.2.1Expression of TNFR1 but not of TNFR2 in dorsal root ganglion neurons and the sensory F-11 cell line....................................................................................................... 534.2.2Cell-specific plasticity of TNFR1 and TNFR2 expression in the dorsal root ganglion after LPS treatment .......................................................................................................... 544.2.3Possible roles of TNFR1 in DRG neurons and of TNFR1 and TNFR2 in DRG non-neuronal cells in pain and other sensory functions.......................................................... 554.2.4Cellular source of TNFαin rat dorsal root ganglion ...................................................... 564.3 Functional implications of IL-1βand IL-1R1 expression in rat dorsal root
ganglion.............................................................................................................. 58 4.3.1Cellular source of IL-1βin rat dorsal root ganglion....................................................... 58
III
5
6
7
8
4.3.2
4.4
Contents
Possible roles of IL-1R1 expression in neuronal and non-neuronal cells of rat dorsal
threshold) or chemical stimuli. Among the pain sensing neurons, there is further
biochemical and functional diversity. Some DRG neurons are classified as peptidergic,
releasing neuropeptides such as calcitonin gene-related peptide (CGRP) and substance
P (SP) in response to noxious thermal stimuli and inflammation (1, 3, 4). All SP-
positive DRG neurons are known to contain CGRP and these neurons are considered
to be a part of nociceptive population of sensory neurons (5, 6). Some neurons are
classified as vanilloid receptor 1 (VR1, also referred to as TRPV1) expressing
neurons, which is essential for the development of inflammatory thermal hyperalgesia
(7-9). VR1, a member of the transient receptor potential (TRP) channel family, is an
non-selective ion channel on sensory neurons that is activated by temperatures
exceeding 43.8°C, and by capsaicin, the main pungent ingredient in hot chili peppers
as well as by protons (7-9). VR1 is expressed predominantly by small-size to
medium-size sensory neurons (8).
One very important function of the primary sensory neurons is to provide the
information about the occurrence or threat of injury. The perception of pain
contributes to this function. Inflammation is the major cause of pain (10). During
inflammation proinflammatory cytokines such as tumor necrosis factor alpha (TNFα)
and interleukin-1 beta (IL-1β)are released by a variety of cells (e.g., macrophages) to 1
Introduction
regulate the inflammatory responses (11). Studies in animals have demonstrated
mechanical and thermal hyperalgesia after systemic or local injection of TNFα, IL-
1βor lipopolysaccharide (LPS) (12-15). Overexpression of proinflammatory
cytokines can lead to systemic syndromes such as septic shock. Therefore, the
responses to TNFα, IL-1β or LPS must be controlled. The question how these
molecules signal to primary sensory neurons of DRG has not yet been resolved.
1.2 TNFαin the dorsal root ganglion
TNFα a multipotent proinflammatory cytokine that induces a wide variety of is
responses including apoptosis in some cells and proliferation in others (16). The
principal physiological function of TNFα is to stimulate the recruitment of
neutrophils and monocytes to the site of infection and to activate these cells to
eradicate microbes. TNFα the principal mediator of the acute inflammatory is
response to Gram-negative bacteria and other infectious microbes and is responsible
for many systemic responses of severe infections such as septic shock, which is
characterized by vascular collapse, disseminated intravascular coagulation, and
metabolic disturbances (17). The activated mononuclear phagocytes are the major
cellular source of TNFα. In addition, T cells can also be a cellular source of TNFαduring the immune response (18). In the nervous system, microglia and astrocytes are
believed to be the primary source of TNFα(19-23). In the peripheral nervous system,
TNFα has been shown to be produced in macrophages and Schwann cells (24, 25).
Recent reports have described the presence of TNFαin primary sensory neurons and
its axonal transport in the intact and injured rat sciatic nerve (26-29). TNFαimmunoreactivity has been detected in a subpopulation of rat DRG neurons and was
reported to be upregulated after chronic constriction injury of the sciatic nerve (28,
29). However, whether TNFαis truly synthesized by primary sensory neurons has not
yet been demonstrated.
1.3 TNF receptor subtypes and their expression in primary
sensory neurons of the dorsal root ganglion
The ability of TNFαto influence cellular functions depends on the expression of TNF
receptors and activation of specific intracellular signaling pathways. There are two
distinct TNF receptors of 55 kD (type I TNF receptor-TNFR1, or p55) and 75 kD
(type II TNF receptor-TNFR2, or p75). The majority of TNFαeffects are transmitted