| Literature DB >> 26914885 |
Marco Giordano1, Francesco Falciglia2, Alessia Poggiaroni2, Angelo Gabriele Aulisa2, Pietro Savignoni2, Vincenzo Guzzanti2,3.
Abstract
INTRODUCTION: The anterior cruciate ligament (ACL) injury is one of the most common in the knee. Tendons can be used as alternative grafts for ACL repair, with tendon "ligamentization" often reported in literature. The purpose of this study was to evaluate the morphological and histological changes occurring in a semitendinosus tendon (ST) during ACL reconstruction in growing rabbits.Entities:
Keywords: Anterior cruciate ligament; Immature animal models; Intra-articular tract; Ligamentization; Semitendinosus tendon
Year: 2015 PMID: 26914885 PMCID: PMC4551549 DOI: 10.1186/s40634-015-0033-1
Source DB: PubMed Journal: J Exp Orthop ISSN: 2197-1153
Fig. 1Carnevali’s technique: intraoperative field. The right knees joint was exposed. The ST and G tendons are divided from the musculo-tendinous junction, preserving the distal insertion site. Once the ACL was accurately removed the oblique 2-mm-diameter tunnels were drilled, mediolaterally in the tibia and anteroposteriorly in the femur (arrows), passing through the original attachments of the ACL and through the growth plates. Then, the semitendinosus tendon (*) was threaded through the tibial and femoral tunnels and then sutured to the periosteum of the lateral part of the femoral metaphysis with 2.0 silk thread
Fig. 2Normal structure of the anterior cruciate ligament in the growing rabbit. H&E staining (a) Original magnification x20; (b) Original magnification x60; (c) Original magnification x100
Fig. 3H&E staining (a) (Original magnification x40) One month after surgery the graft tissue showed regions of cell-free areas and necrosis. *Vessel located in the periphery of the graft and runned parallel to the collagen fiber bundles in the septa at forty days; b (Original magnification x100) fusiform fibroblast (arrow) in the central portion of the tendon. c Masson trichrome staining (Original magnification x40) Disorganized collagenous fibers at 4 weeks
Fig. 4H&E staining (a) (Original magnification x40). Fibroblastic cells of the semitendinosus tendon at 2 months after surgery. b (Original magnification x100). Fibroblastic cells with large nuclei and abundant cytoplasm 8 weeks after surgery. c Masson trichrome staining (Original magnification x60) Collagenous fibers of the semitendinosus tendon at 8 weeks after surgery
Fig. 5Peripheral and core vessels(*) in the semitendinosus tendon 24 weeks after surgery. a H&E staining (Original magnification x40). b Masson trichrome staining (Original magnification x40) (c) Alcian Blue (Original magnification x20)
Fig. 6a H&E staining (Original magnification x60). Despite the histological changes the neoligament at 48 weeks after surgery does not assume the characteristics of the normal rabbits ACL. The fibers showed a slight separation with increased waviness. The cellularity and vascularity were graded as normal. The fibrocytes have different characteristics from the fibroblastic cells observed few time after surgery. b Masson trichrome staining (Original magnification x20). Semitendinosus tendon 48 weeks after surgery. An increased longitudinal and parallel orientation of the collagen bundles was observed; c Masson trichrome staining (Original magnification x40). At 48 weeks the neoligament was viable. Red cells were present in the peripheric portion of the graft
Major histological characteristics at each time-point in ST graft
| 1 week | 4 weeks | 6 weeks | 8 weeks | 12 weeks | 24 weeks | 48 weeks | |
|---|---|---|---|---|---|---|---|
| Necrosis | Focal cell-free areas with small necrosis | Cell-free areas with poor necrosis | Gradually disappeares | No necrosis sign | |||
| Neovascularization | No vessel | Poor and located on the grafts periphery | Vessel located in the periphery of the graft and runned parallel to the collagen fiber bundles in the septa | Vessel located from periphery to central area | Normal vascularity | ||
| Organization of the collagen fibers | ST tendon characteristics | Disorganized collagenous fibers | Initial longitudinal arrangement | Collagen fibers aligned in parallel with the new capillaries and with the fibroblastic cells | Loss of regular collagen orientation and crimp pattern | Slight separation with increased waviness of fibers | |
| Shift of the diameter of the collagen fibrils, from large to small | Unimodal appearance of collagen fibrils | ||||||
| Reduction of collagen type I fibrils | Failure restauration of collagen orientation to normality | ||||||
| Increase of collagen type III synthesis | |||||||
| Cellularity | Inflammatory cell population | Aligned longitudinally, more rounded fibroblastic cells with large nuclei and abundant cytoplasm | Highly differentiated fibroblastic cells | Normal cellularity | |||
| Disorganized and randomly arranged fusiform-like fibroblastic cells with plump nuclei | Gradual disappearance of the typical inflammatory cell population | Fibrocyte have different characteristics from fibroblastic cells | |||||