Laino Gregorio, d'Aquino Riccardo, Graziano Antonio, Lanza Vladimiro, Carinci Francesco, Naro Fabio, Pirozzi Giuseppe, Papaccio Gianpaolo
Dipartimento di Medicina Sperimentale, Sezione Istologia ed Embriologia, Secondo Ateneo di Napoli, Napoli, Italy.
J Bone Miner Res. 2005 Aug;20(8):1394-402. doi: 10.1359/JBMR.050325. Epub 2005 Mar 28.
Stem cells, derived from human adult dental pulp of healthy subjects 30-45 years of age, were cultured, and cells were selected using a FACSorter. A new c-kit+/CD34+/CD45- cell population of stromal bone producing cells (SBP/DPSCs) was selected, expanded, and cultured. These SBP/DPSCs are highly clonogenic and, in culture, differentiate into osteoblast precursors (CD44+/RUNX-2+), still capable of self-renewing, and then in osteoblasts, producing, in vitro, a living autologous fibrous bone (LAB) tissue, which is markedly positive for several bone antibodies. This tissue constitute an ideal source of osteoblasts and mineralized tissue for bone regeneration. In fact, after in vivo transplantation into immunocompromised rats, LAB formed lamellar bone-containing osteocytes.
Recently it has been reported that human dental pulp stem cells (DPSCs) are detectable, in humans, only up to the age of 30 years and that they are able to produce in vitro only sporadic calcified nodules and to form, after transplantation in vivo, a mineralized tissue.
Stem cells, derived from human adult dental pulp of healthy subjects 30-45 years of age, were cultured, and cells were selected using a FACSorter. Light microscope, histochemistry, immunofluorescence, and RT-PCR analyses were performed to study both stem and differentiating cells.
A new c-kit+/CD34+/CD45- cell population of stromal bone producing cells (SBP/DPSCs) has been selected by FACSorting, expanded, and cultured. These SBP/DPSCs are highly clonogenic and, in culture, differentiate into osteoblast precursors (CD44+/RUNX-2+), still capable of self-renewing, and in osteoblasts, producing, in vitro, a living autologous fibrous bone (LAB) tissue. This new-formed tissue is markedly positive for several antibodies for bone, including osteonectin, bone sialoprotein, osteocalcin, fibronectin, collagen III, and bone alkaline phosphatase (BALP). Cells producing LAB can be stored at -80 degrees C for a long period of time and are an extraordinary source of osteoblasts and mineralized fibrous bone tissue. In this study, we also showed that, in aged humans, stem cells can be detected from their pulps. The produced LAB is a fibrous bone tissue resembling the human bone during mineralization, with an external layer formed by osteoblasts markedly positive for osteocalcin. This newly formed tissue constitute an ideal source of osteoblasts and mineralized tissue for bone regeneration. In fact, after in vivo transplantation into immunocompromised rats, LAB formed lamellar bone containing osteocytes.
从30至45岁健康受试者的成人牙髓中提取干细胞进行培养,并使用荧光激活细胞分选仪(FACSorter)筛选细胞。筛选出一种新的基质骨生成细胞(SBP/DPSC)群体,即c-kit+/CD34+/CD45-细胞群体,进行扩增和培养。这些SBP/DPSC具有高度克隆性,在培养过程中可分化为成骨细胞前体(CD44+/RUNX-2+),仍具有自我更新能力,然后分化为成骨细胞,在体外产生一种活的自体纤维骨(LAB)组织,该组织对多种骨抗体呈明显阳性。这种组织构成了用于骨再生的成骨细胞和矿化组织的理想来源。事实上,将LAB体内移植到免疫缺陷大鼠后,形成了含骨细胞的板层骨。
最近有报道称,人类牙髓干细胞(DPSC)在人类中仅在30岁之前可检测到,并且它们在体外仅能产生散在的钙化结节,在体内移植后形成矿化组织。
从30至45岁健康受试者的成人牙髓中提取干细胞进行培养,并使用荧光激活细胞分选仪筛选细胞。进行光镜、组织化学、免疫荧光和逆转录-聚合酶链反应(RT-PCR)分析以研究干细胞和分化细胞。
通过荧光激活细胞分选筛选出一种新的基质骨生成细胞(SBP/DPSC)群体,即c-kit+/CD34+/CD45-细胞群体,进行扩增和培养。这些SBP/DPSC具有高度克隆性,在培养过程中可分化为成骨细胞前体(CD44+/RUNX-2+),仍具有自我更新能力,并分化为成骨细胞,在体外产生一种活的自体纤维骨(LAB)组织。这种新形成的组织对多种骨抗体呈明显阳性,包括骨连接蛋白、骨唾液蛋白、骨钙素、纤连蛋白、胶原蛋白III和骨碱性磷酸酶(BALP)。产生LAB的细胞可在-80℃长期保存,是成骨细胞和矿化纤维骨组织的非凡来源。在本研究中,我们还表明,在老年人类中,可从其牙髓中检测到干细胞。产生的LAB是一种在矿化过程中类似于人类骨骼的纤维骨组织,其外层由对骨钙素呈明显阳性的成骨细胞形成。这种新形成的组织构成了用于骨再生的成骨细胞和矿化组织的理想来源。事实上,将LAB体内移植到免疫缺陷大鼠后,形成了含骨细胞的板层骨。