The purpose of this study was to determine whether the transplantation of human cells from a nonâreattached injured anterior cruciate ligament (ACL) remnant could enhance tendonâbone healing. Human ACL remnant tissue was classified into two groups based on the morphologic pattern as per Crain's classification: (1) nonâreattachment group (Crain â
Ł) and (2) reattachment group (Crain â
ââ
˘). Seventyâfive 10âweekâold immunodeficient rats underwent ACL reconstruction followed by intracapsular administration of one of the following: (1) ACLâderived cells from the nonâreattached remnant (nonâreattachment group) (nâ=â5), (2) ACLâderived cells from the reattached tissue (reattachment group) (nâ=â5), or (3) phosphateâbuffered saline (PBS) only (PBS group) (nâ=â5). Histological (Weeks 2, 4, and 8), immunohistochemical (Week 2), radiographic (Weeks 0, 2, 4, and 8), and biomechanical (Week 8) assessments were performed. Histological evaluation showed high and early healing, induction of endochondral ossificationâlike integration, and mature bone ingrowth at Week 4 in the nonâreattachment group. Microcomputed tomography at Week 4 showed that the tibial bone tunnels in the nonâreattachment group were significantly reduced compared to those in the reattachment and PBS groups. Moreover, biomechanical testing showed that ultimate loadâtoâfailure in the nonâreattachment group tended to be larger than that in the reattachment group, though not statistically significant. The enhanced healing potential in the nonâreattachment group was explained by the increase in intrinsic angiogenesis/osteogenesis. In the subacute phase, the ACLâderived cells with the nonâreattached morphologic pattern showed greater and earlier tendon bone healing compared with the cells obtained from the reattached morphologic pattern.