Advanced Search

Journal Navigation

Journal Home

Subscriptions

Archive

Contact Us

Table of Contents

Click here to sign up for SAGE Journal Email Alerts today!

Sign In to gain access to subscriptions and/or personal tools.
Journal of Dental Research
Right arrow Help viewing high resolution images
Right arrow Return to article
Click on image to view larger version.


Figure 3


Figure 3. In vivo characterization of cryopreserved periodontal ligament stem cells. (A) After 8 wks of transplantation, cryopreserved periodontal ligament stem cells were capable of forming a cementum-like structure (C) on the surfaces of the hydroxyapatite/tricalcium phosphate (HA) carrier, which was connected to periodontal-ligament-like tissue (PDL). (B) The cells responsible for cementum (C) formation were positive for anti-human specific mitochondria antibody staining (black arrows). Analysis of the immunohistochemical staining data indicated that transplanted cryopreserved periodontal ligament stem cells differentiated into cementoblasts/cementocytes and generated cementum in vivo. (C,D) Transplanted cryopreserved periodontal ligament stem cells were able to form cementum (C) on the surfaces of HA/TCP particles (HA) and were able to generate Sharpey’s fibers (black arrows) inserted into cementum and which were continuous with periodontal-ligament-like tissue (PDL), shown by H&E (C) and Trichrome staining (D). (E,F) Of 6 selected single-colony-derived cryopreserved periodontal ligament stem cell strains, only 4 (67%) were capable of generating a cementum/periodontal-ligament-like structure (E). Newly formed cementum (C) was found to be adjacent to the surfaces of the HA/TCP carrier (HA) and was connected with periodontal-ligament-like tissue (PDL) that was the same as Sharpey’s fibers (back arrows). The remaining 33% (2 of 6) single-colony-derived cryopreserved periodontal ligament stem cell strains were unable to generate cementum in vivo (F). (G,H) Newly formed cementum (C) was positive for anti-type I collagen antibody staining (G), and cementogenic cells were positive for anti-bone sialoprotein (BSP) antibody staining (open arrows in H). (I) Pre-immunoserum control was negative for immunohistochemical staining of type I collagen and BSP antibodies (scale bar, 50 µm for A-I).

J DENT RES, Vol. 84, No. 10, 907-912 (2005)
DOI: 10.1177/154405910508401007





Right arrow Return to article