Abstract:The distribution and ultrastructure of class II major histocompatibility complex (MHC)-positive cells were investigated in human dental pulp, employing immunohistochemistry using an anti-human leukocyte antigen (HLA)-DR-monoclonal antibody. HLA-DR-immunopositive cells, appearing spindle-like or dendritic in profile, were densely distributed throughout the dental pulp. Under the electron microscope, these cells exhibited various sizes of vesicles containing clear or opaque contents, multivesicular bodies and ch… Show more
“…These class II MHC-positive cells along the pulp-dentin border were characterized by tubulovesicular structures and multivesicular bodies, as categorized in the pulpal dendritic cells described above (Ohshima et al, 1994(Ohshima et al, , 1999. This phenomenon may be explained by the idea that the pulpal dendritic cells respond actively to bacterial or noxious substances derived through the exposed dentinal tubules, as we have suggested .…”
Section: Discussionmentioning
confidence: 70%
“…Interestingly, under experimental conditions, the class II MHC-positive cells have been suggested to have diverse functions in odontoblast differentiation in the rat dental pulp in addition to ordinary antigen presentation . Under physiological conditions, furthermore, class II MHC-positive cells in the human odontoblast layer and/or predentin might have some regulatory function in the homeostasis of odontoblasts (Ohshima et al, 1999). These findings, therefore, lead us to the possibility that the immunocompetent cells play an important role in the process of pulpal healing after cavity preparation.…”
The regeneration process of the odontoblast cell layer incident to tooth injury, especially its relationship with immunocompetent cells in pulp healing, has not been fully understood. The purpose of the present study was to clarify this relationship between odontoblasts and immunocompetent cells in the process of pulp regeneration following cavity preparation in rat molars by immunocytochemistry for heat shock protein (Hsp) 25 as well as class II major histocompatibility complex (MHC) molecules. In untreated control teeth, intense Hsp 25-immunoreactivity was found in the cell bodies of odontoblasts and their processes within the predentin, whereas class II MHC-positive cells were predominantly located beneath the odontoblast cell layer. Cavity preparation caused the destruction of the odontoblast layer to form an edematous lesion and the shift of class II MHC-positive cells with the injured odontoblasts toward the pulp core at the affected site. Some damaged odontoblasts without apparent cytoplasmic processes, round in profile, retained the immunoreactivity for Hsp25, suggesting the survival of a part of the odontoblasts against artificial external stimuli. Twelve hours after cavity preparation, numerous class II MHC-positive cells appeared along the pulp-dentin border and extended their processes deep into the exposed dentinal tubules. By postoperative 72 hours, newly differentiated odontoblasts with Hsp 25-immunoreactivity were arranged at the pulp-dentin border, but the class II MHC-positive cells moved from the pulp-dentin border to the subodontoblastic layer. These findings indicate that the time course of changes in the expression of Hsp 25-immunoreactivity reflects the regeneration process of odontoblasts. The functional roles of Hsp 25-positive odontoblasts and immunocompetent cells such as class II MHC-positive cells in the process of pulp regeneration after cavity preparation are discussed in conjunction with our previous experimental data.
“…These class II MHC-positive cells along the pulp-dentin border were characterized by tubulovesicular structures and multivesicular bodies, as categorized in the pulpal dendritic cells described above (Ohshima et al, 1994(Ohshima et al, , 1999. This phenomenon may be explained by the idea that the pulpal dendritic cells respond actively to bacterial or noxious substances derived through the exposed dentinal tubules, as we have suggested .…”
Section: Discussionmentioning
confidence: 70%
“…Interestingly, under experimental conditions, the class II MHC-positive cells have been suggested to have diverse functions in odontoblast differentiation in the rat dental pulp in addition to ordinary antigen presentation . Under physiological conditions, furthermore, class II MHC-positive cells in the human odontoblast layer and/or predentin might have some regulatory function in the homeostasis of odontoblasts (Ohshima et al, 1999). These findings, therefore, lead us to the possibility that the immunocompetent cells play an important role in the process of pulpal healing after cavity preparation.…”
The regeneration process of the odontoblast cell layer incident to tooth injury, especially its relationship with immunocompetent cells in pulp healing, has not been fully understood. The purpose of the present study was to clarify this relationship between odontoblasts and immunocompetent cells in the process of pulp regeneration following cavity preparation in rat molars by immunocytochemistry for heat shock protein (Hsp) 25 as well as class II major histocompatibility complex (MHC) molecules. In untreated control teeth, intense Hsp 25-immunoreactivity was found in the cell bodies of odontoblasts and their processes within the predentin, whereas class II MHC-positive cells were predominantly located beneath the odontoblast cell layer. Cavity preparation caused the destruction of the odontoblast layer to form an edematous lesion and the shift of class II MHC-positive cells with the injured odontoblasts toward the pulp core at the affected site. Some damaged odontoblasts without apparent cytoplasmic processes, round in profile, retained the immunoreactivity for Hsp25, suggesting the survival of a part of the odontoblasts against artificial external stimuli. Twelve hours after cavity preparation, numerous class II MHC-positive cells appeared along the pulp-dentin border and extended their processes deep into the exposed dentinal tubules. By postoperative 72 hours, newly differentiated odontoblasts with Hsp 25-immunoreactivity were arranged at the pulp-dentin border, but the class II MHC-positive cells moved from the pulp-dentin border to the subodontoblastic layer. These findings indicate that the time course of changes in the expression of Hsp 25-immunoreactivity reflects the regeneration process of odontoblasts. The functional roles of Hsp 25-positive odontoblasts and immunocompetent cells such as class II MHC-positive cells in the process of pulp regeneration after cavity preparation are discussed in conjunction with our previous experimental data.
“…13 Although the function of these cells is not clearly understood, anatomical proximity and functional coupling through gap junctions implies a regulatory role. 14 Interodontoblastic cells could be involved in the response of odontoblasts to bacterial challenge, and they may be necessary for an integrated response to bacterial invasion.…”
We report evidence for anatomical and functional changes of dental pulp in response to bacterial invasion through dentin that parallel responses to noxious stimuli reported in neural crest-derived sensory tissues. Sections of resin-embedded carious adult molar teeth were prepared for immunohistochemistry, in situ hybridization , ultrastructural analysis , and microdissection to extract mRNA for quantitative analyses. In odontoblasts adjacent to the leading edge of bacterial invasion in carious teeth , expression levels of the gene encoding dentin sialo-protein were 16-fold greater than in odontoblasts of healthy teeth, reducing progressively with distance from this site of the carious lesion. In contrast , gene expression for dentin matrix protein-1 by odontoblasts was completely suppressed in carious teeth relative to healthy teeth. These changes in gene expression were related to a gradient of deposited reactionary dentin that displayed a highly modified structure. In carious teeth , interodontoblastic dentin sialo-protein ؊ cells expressing glutamine synthetase (GS) showed up-regulation of glial fibrillary acidic protein (GFAP
“…Dendritic cells show no or little activity of acid phosphatase (ACP), whereas macrophages have phagocytic capability and exhibit ACP activity that is dependent on the phagocytic capability (Steinman et al 1986). Class II MHC antigen-expressing cells have been identified in the dental pulp of humans and rats by immunohistochemistry using HLA-DR and OX-6 antibodies (Jontell et al 1987(Jontell et al , 1988(Jontell et al , 1991(Jontell et al , 1994Ohshima et al 1994Ohshima et al , 1995Ohshima et al , 1999Okiji et al 1994Okiji et al , 1996Okiji et al , 1997Yoshiba et al 1996). Based on the criteria of the expression of class II MHC antigens and the activity of ACP, previous studies have indicated that, whereas macrophages are present in the central region of the dental pulp, dendritic cells are located in and around the odontoblastic layer.…”
Section: Introductionmentioning
confidence: 98%
“…The immunological aspects in pulpal tissue and the putative function of these cells were reviewed by Jontell et al (1998). It has been suggested that the class II MHC-expressing dendritic cells in the odontoblastic layer may regulate the function of odontoblasts and play a role in odontoblast differentiation in human and rat teeth (Ohshima et al 1995(Ohshima et al , 1999, and class II MHC-positive cells have been suggested to play an inductive role in differentiation, migration, and/or activation of odontoblasts and cementoblast-like cells during the resorption stage of human deciduous teeth (Kannari et al 1998). In addition, age-related change and delayed appearance of class II MHC-positive cells have been reported in dental pulp during development of rat incisors and molars (Jontell et al 1991;Okiji et al 1996).…”
Dendritic cells and macrophages were examined in dental pulp during the postnatal development of mouse mandibular first molars, by immuno- and enzyme histochemistry. F4/80 antibody against dendritic cells and macrophages demonstrated labeled cells predominantly in and around the odontoblastic layer during tooth development from postnatal day 0 (PN0) to PN5. Labeling with Mac-1, Mac-2, and MOMA-2 antibodies against macrophages showed varied distribution patterns. Mac-1-positive cells were not detected in the dental pulp. Mac-2-positive cells appeared in the dental pulp at PN0, but not in or around the odontoblastic layer, and disappeared by PN3. A few MOMA-2-positive cells were detected in the dental pulp during the period examined. The F4/80-positive cells in and around the odontoblastic layer did not exhibit acid phosphatase or non-specific esterase activities. In addition, the F4/80-positive cells showed continued expression of Fcgamma receptor, but not class II major histocompatibility complex (MHC). Other antibodies against dendritic cells (NLDC-145, MIDC-8, and 33D1) did not label the F4/80-positive cells. We concluded that the F4/80-positive and class II MHC-negative cells in and around the odontoblastic layer may be immature dendritic cells in the early stages before eruption, weaning, and crucial exposure to antigenic stimuli. They may not only act primarily as immunosurveillance cells, but also play a role in a regulatory function and differentiation of odontoblasts.
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