Reassessing the genetic lineage tracing of lingual Lgr5+ and Lgr6+ cells in vivo

Taste buds, the neuroepithelial organs responsible for the detection of gustatory stimuli in the oral cavity, arise from stem/progenitor cells among nearby basal keratinocytes. Using genetic lineage tracing, Lgr5 and Lgr6 were suggested as the specific markers for the stem/progenitor cells of taste...

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Published inAnimal cells and systems Vol. 28; no. 1; pp. 353 - 366
Main Authors Kim, Hyun Ji, Seo, Dong Woo, Shim, Jaewon, Lee, Jun-Seok, Choi, Sang-Hyun, Kim, Dong-Hoon, Moon, Seok Jun, Jung, Han-Sung, Jeong, Yong Taek
Format Journal Article
LanguageEnglish
Published England Taylor & Francis 31.12.2024
Taylor & Francis Ltd
Taylor & Francis Group
한국통합생물학회
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ISSN1976-8354
2151-2485
2151-2485
DOI10.1080/19768354.2024.2381578

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Summary:Taste buds, the neuroepithelial organs responsible for the detection of gustatory stimuli in the oral cavity, arise from stem/progenitor cells among nearby basal keratinocytes. Using genetic lineage tracing, Lgr5 and Lgr6 were suggested as the specific markers for the stem/progenitor cells of taste buds, but recent evidence implied that taste buds may arise even in the absence of these markers. Thus, we wanted to verify the genetic lineage tracing of lingual Lgr5- and Lgr6-expressing cells. Unexpectedly, we found that antibody staining revealed more diverse Lgr5-expressing cells inside and outside the taste buds of circumvallate papillae than was previously suggested. We also found that, while tamoxifen-induced genetic recombination occurred only in cells expressing the Lgr5 reporter GFP, we did not see any increase in the number of recombined daughter cells induced by consecutive injections of tamoxifen. Similarly, we found that cells expressing Lgr6, another stem/progenitor cell marker candidate and an analog of Lgr5, also do not generate recombined clones. In contrast, Lgr5-expressing cells in fungiform papillae can transform into Lgr5-negative progeny. Together, our data indicate that lingual Lgr5- and Lgr6-expressing cells exhibit diversity in their capacity to transform into Lgr5- and Lgr6-negative cells, depending on their location. Our results complement previous findings that did not distinguish this diversity.
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Supplemental data for this article can be accessed online at https://doi.org/10.1080/19768354.2024.2381578.
ISSN:1976-8354
2151-2485
2151-2485
DOI:10.1080/19768354.2024.2381578