Plap-1 lineage tracing and single-cell transcriptomics reveal cellular dynamics in the periodontal ligament

Author:

Iwayama Tomoaki1ORCID,Iwashita Mizuho1,Miyashita Kazuya2,Sakashita Hiromi13,Matsumoto Shuji1,Tomita Kiwako1,Bhongsatiern Phan1,Kitayama Tomomi24,Ikegami Kentaro2,Shimbo Takashi34,Tamai Katsuto4,Murayama Masanori A.5ORCID,Ogawa Shuhei5,Iwakura Yoichiro5ORCID,Yamada Satoru6,Olson Lorin E.7ORCID,Takedachi Masahide1ORCID,Murakami Shinya1ORCID

Affiliation:

1. Osaka University Graduate School of Dentistry 1 Department of Periodontology , , Suita, Osaka 565-0871 , Japan

2. StemRIM Inc. 2 , Ibaraki, Osaka 567-0085 , Japan

3. StemRIM Institute of Regeneration-Inducing Medicine, Osaka University 3 , Suita 565-0871 , Japan

4. Osaka University Graduate School of Medicine 4 Department of Stem Cell Therapy Science , , Osaka 565-0871 , Japan

5. Research Institute for Biomedical Sciences, Tokyo University of Science 5 , Noda, Chiba 278-8510 , Japan

6. Tohoku University Graduate School of Dentistry 6 Department of Periodontology and Endodontology , , Sendai, Miyagi 980-8575 , Japan

7. Cardiovascular Biology Research Program, Oklahoma Medical Research Foundation 7 , Oklahoma City, OK 73104 , USA

Abstract

ABSTRACT Periodontal tissue supports teeth in the alveolar bone socket via fibrous attachment of the periodontal ligament (PDL). The PDL contains periodontal fibroblasts and stem/progenitor cells, collectively known as PDL cells (PDLCs), on top of osteoblasts and cementoblasts on the surface of alveolar bone and cementum, respectively. However, the characteristics and lineage hierarchy of each cell type remain poorly defined. This study identified periodontal ligament associated protein-1 (Plap-1) as a PDL-specific extracellular matrix protein. We generated knock-in mice expressing CreERT2 and GFP specifically in Plap-1-positive PDLCs. Genetic lineage tracing confirmed the long-standing hypothesis that PDLCs differentiate into osteoblasts and cementoblasts. A PDL single-cell atlas defined cementoblasts and osteoblasts as Plap-1−Ibsp+Sparcl1+ and Plap-1−Ibsp+Col11a2+, respectively. Other populations, such as Nes+ mural cells, S100B+ Schwann cells, and other non-stromal cells, were also identified. RNA velocity analysis suggested that a Plap-1highLy6a+ cell population was the source of PDLCs. Lineage tracing of Plap-1+ PDLCs during periodontal injury showed periodontal tissue regeneration by PDLCs. Our study defines diverse cell populations in PDL and clarifies the role of PDLCs in periodontal tissue homeostasis and repair.

Funder

Japan Society for the Promotion of Science

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

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