{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,18]],"date-time":"2026-08-18T01:10:57Z","timestamp":1787015457777,"version":"build-2736575974"},"reference-count":31,"publisher":"Wiley","issue":"4","license":[{"start":{"date-parts":[[2020,1,19]],"date-time":"2020-01-19T00:00:00Z","timestamp":1579392000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Acad Dermatol Venereol"],"published-print":{"date-parts":[[2020,4]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:sec>\n                    <jats:title>Background<\/jats:title>\n                    <jats:p>Chancre self\u2010healing is an important clinical feature in the early stages of syphilis infection. Wound healing may involve an important mechanism by the migration of fibroblasts filling the injured lesion. However, the specific mechanism underlying this process is still unknown.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Objectives<\/jats:title>\n                    <jats:p>We aimed to analyse the role of Tp0136 in the migration of fibroblasts and the related mechanism.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>\n                      The migration ability of fibroblasts was detected by a wound\u2010healing assay.\n                      <jats:styled-content style=\"fixed-case\">RT<\/jats:styled-content>\n                      \u2010\n                      <jats:styled-content style=\"fixed-case\">PCR<\/jats:styled-content>\n                      and\n                      <jats:styled-content style=\"fixed-case\">ELISA<\/jats:styled-content>\n                      detected the expression of\n                      <jats:styled-content style=\"fixed-case\">MCP<\/jats:styled-content>\n                      \u20101,\n                      <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\n                      \u20106 and\n                      <jats:styled-content style=\"fixed-case\">MMP<\/jats:styled-content>\n                      \u20109.\n                      <jats:styled-content style=\"fixed-case\">TLR<\/jats:styled-content>\n                      4 expression was detected by\n                      <jats:styled-content style=\"fixed-case\">RT<\/jats:styled-content>\n                      \u2010\n                      <jats:styled-content style=\"fixed-case\">PCR<\/jats:styled-content>\n                      . The protein levels of\n                      <jats:styled-content style=\"fixed-case\">CCR<\/jats:styled-content>\n                      2 and relevant signalling pathway molecules were measured by Western blotting.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      Tp0136 significantly promoted fibroblast migration. Subsequently, the levels of\n                      <jats:styled-content style=\"fixed-case\">MCP<\/jats:styled-content>\n                      \u20101 and its receptor\n                      <jats:styled-content style=\"fixed-case\">CCR<\/jats:styled-content>\n                      2 were increased in this process. The migration of fibroblasts was significantly inhibited by an anti\u2010\n                      <jats:styled-content style=\"fixed-case\">MCP<\/jats:styled-content>\n                      \u20101 neutralizing antibody or\n                      <jats:styled-content style=\"fixed-case\">CCR<\/jats:styled-content>\n                      2 inhibitors. Furthermore, studies demonstrated that Tp0136 could activate the\n                      <jats:styled-content style=\"fixed-case\">ERK<\/jats:styled-content>\n                      \/\n                      <jats:styled-content style=\"fixed-case\">JNK<\/jats:styled-content>\n                      \/\n                      <jats:styled-content style=\"fixed-case\">PI<\/jats:styled-content>\n                      3K\/\n                      <jats:styled-content style=\"fixed-case\">NF<\/jats:styled-content>\n                      \u2010\u03baB signalling pathways through\n                      <jats:styled-content style=\"fixed-case\">TLR<\/jats:styled-content>\n                      4 activity and that signalling pathways inhibitors could weaken\n                      <jats:styled-content style=\"fixed-case\">MCP<\/jats:styled-content>\n                      \u20101 secretion and fibroblast migration.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>\n                      These findings demonstrate that Tp0136 promotes the migration of fibroblasts by inducing\n                      <jats:styled-content style=\"fixed-case\">MCP<\/jats:styled-content>\n                      \u20101\/\n                      <jats:styled-content style=\"fixed-case\">CCR<\/jats:styled-content>\n                      2 expression through signalling involving the\n                      <jats:styled-content style=\"fixed-case\">TLR<\/jats:styled-content>\n                      4,\n                      <jats:styled-content style=\"fixed-case\">ERK<\/jats:styled-content>\n                      ,\n                      <jats:styled-content style=\"fixed-case\">JNK<\/jats:styled-content>\n                      ,\n                      <jats:styled-content style=\"fixed-case\">PI<\/jats:styled-content>\n                      3K and\n                      <jats:styled-content style=\"fixed-case\">NF<\/jats:styled-content>\n                      \u2010\u03baB signalling pathways, which could contribute to the mechanism of chancre self\u2010healing in syphilis.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1111\/jdv.16162","type":"journal-article","created":{"date-parts":[[2019,12,19]],"date-time":"2019-12-19T12:01:38Z","timestamp":1576756898000},"page":"862-872","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":18,"title":["Recombinant\n                    <i>Treponema pallidum<\/i>\n                    protein Tp0136 promotes fibroblast migration by modulating\n                    <scp>MCP<\/scp>\n                    \u20101\/\n                    <scp>CCR<\/scp>\n                    2 through\n                    <scp>TLR<\/scp>\n                    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