Division of Pediatric Endocrinology and Center for Molecular Medicine, L8:01, Department of Women's and Children's Health, Karolinska Institutet and University Hospital, Stockholm, Sweden.
Department of Surgical Sciences, Uppsala University, Uppsala, Sweden; Department of Orthopedics, Falu Lasarett, Lasarettsvägen 10, 791 82, Falun, Sweden.
Bone. 2021 Oct;151:116035. doi: 10.1016/j.bone.2021.116035. Epub 2021 Jun 8.
Perichondrium autotransplants have been used to reconstruct articular surfaces destroyed by infection or trauma. However, the role of the transplanted perichondrium in the healing of resurfaced joints has not been investigated.
Perichondrial and periosteal tissues were harvested from rats hemizygous for a ubiquitously expressed enhanced green fluorescent protein (EGFP) transgene and transplanted into full-thickness articular cartilage defects at the trochlear groove of distal femur in wild-type littermates. As an additional control, cartilage defects were left without a transplant (no transplant control). Distal femurs were collected 3, 14, 56, 112 days after surgery.
Tracing of transplanted cells showed that both perichondrium and periosteum transplant-derived cells made up the large majority of the cells in the regenerated joint surfaces. Perichondrium transplants contained SOX9 positive cells and with time differentiated into a hyaline cartilage that expanded and filled out the defects with Col2a1-positive and Col1a1-negative chondrocytes and a matrix rich in proteoglycans. At later timepoints the cartilaginous perichondrium transplants were actively remodeled into bone at the transplant-bone interface and at post-surgery day 112 EGFP-positive perichondrium cells at the articular surface were positive for Prg4. Periosteum transplants initially lacked SOX9 expression and despite a transient increase in SOX9 expression and chondrogenic differentiation, remained Col1a1 positive, and were continuously thinning as periosteum-derived cells were incorporated into the subchondral compartment.
Perichondrium and periosteum transplanted to articular cartilage defects did not just stimulate regeneration but were themselves transformed into cartilaginous articular surfaces. Perichondrium transplants developed into an articular-like, hyaline cartilage, whereas periosteum transplants appeared to produce a less resilient fibro-cartilage.
耳软骨自体移植已被用于重建因感染或创伤而受损的关节表面。然而,移植的耳软骨在修复后的关节愈合中的作用尚未得到研究。
从半合子泛表达增强型绿色荧光蛋白(EGFP)转基因大鼠中采集耳软骨和骨膜组织,并将其移植到野生型同窝仔鼠的股骨滑车全层关节软骨缺损处。作为额外的对照,软骨缺损处未进行移植(无移植对照)。术后 3、14、56、112 天收集股骨远端。
移植细胞的示踪表明,耳软骨和骨膜移植来源的细胞构成了再生关节表面细胞的绝大多数。耳软骨移植中含有 SOX9 阳性细胞,随着时间的推移,分化为透明软骨,填充和填满缺损,由 Col2a1 阳性和 Col1a1 阴性软骨细胞和富含蛋白聚糖的基质组成。在后期,软骨化的耳软骨移植在移植-骨界面处被积极重塑为骨,并且在术后 112 天,关节表面的 EGFP 阳性耳软骨细胞对 Prg4 呈阳性。骨膜移植最初缺乏 SOX9 表达,尽管 SOX9 表达和软骨分化短暂增加,但仍保持 Col1a1 阳性,并随着骨膜来源细胞被纳入软骨下腔而不断变薄。
移植到关节软骨缺损处的耳软骨和骨膜不仅刺激了再生,而且自身也转化为软骨关节表面。耳软骨移植发展为类似关节的透明软骨,而骨膜移植似乎产生了一种弹性较差的纤维软骨。