Fisher Jason C, Bodenstein Lawrence
Division of Pediatric Surgery, Morgan Stanley Children's Hospital of New York-Presbyterian and Department of Surgery, College of Physicians and Surgeons, Columbia University, 3959 Broadway, 216B, New York, NY 10032, USA.
Theor Biol Med Model. 2006 Feb 17;3:9. doi: 10.1186/1742-4682-3-9.
Congenital diaphragmatic hernia (CDH) is a birth defect with significant morbidity and mortality. Knowledge of diaphragm morphogenesis and the aberrations leading to CDH is limited. Although classical embryologists described the diaphragm as arising from the septum transversum, pleuroperitoneal folds (PPF), esophageal mesentery and body wall, animal studies suggest that the PPF is the major, if not sole, contributor to the muscular diaphragm. Recently, a posterior defect in the PPF has been identified when the teratogen nitrofen is used to induce CDH in fetal rodents. We describe use of a cell-based computer modeling system (Nudge++) to study diaphragm morphogenesis.
Key diaphragmatic structures were digitized from transverse serial sections of paraffin-embedded mouse embryos at embryonic days 11.5 and 13. Structure boundaries and simulated cells were combined in the Nudge++ software. Model cells were assigned putative behavioral programs, and these programs were progressively modified to produce a diaphragm consistent with the observed anatomy in rodents. Homology between our model and recent anatomical observations occurred under the following simulation conditions: (1) cell mitoses are restricted to the edge of growing tissue; (2) cells near the chest wall remain mitotically active; (3) mitotically active non-edge cells migrate toward the chest wall; and (4) movement direction depends on clonal differentiation between anterior and posterior PPF cells.
With the PPF as the sole source of mitotic cells, an early defect in the PPF evolves into a posteromedial diaphragm defect, similar to that of the rodent nitrofen CDH model. A posterolateral defect, as occurs in human CDH, would be more readily recreated by invoking other cellular contributions. Our results suggest that recent reports of PPF-dominated diaphragm morphogenesis in the rodent may not be strictly applicable to man. The ability to recreate a CDH defect using a combination of experimental data and testable hypotheses gives impetus to simulation modeling as an adjunct to experimental analysis of diaphragm morphogenesis.
先天性膈疝(CDH)是一种具有较高发病率和死亡率的出生缺陷。关于膈肌形态发生以及导致CDH的畸变的知识有限。尽管经典胚胎学家将膈肌描述为由横隔、胸腹皱襞(PPF)、食管系膜和体壁发育而来,但动物研究表明,PPF即便不是唯一的,也是肌肉性膈肌的主要贡献者。最近,当使用致畸剂硝呋烯腙诱导胎鼠发生CDH时,已确定PPF存在后部缺陷。我们描述了使用基于细胞的计算机建模系统(Nudge++)来研究膈肌形态发生。
在胚胎第11.5天和13天,从石蜡包埋的小鼠胚胎的横向连续切片中对关键的膈肌结构进行数字化处理。结构边界和模拟细胞在Nudge++软件中进行组合。为模型细胞分配假定的行为程序,并逐步修改这些程序,以生成与啮齿动物中观察到的解剖结构一致的膈肌。在以下模拟条件下,我们的模型与最近的解剖学观察结果具有同源性:(1)细胞有丝分裂仅限于生长组织的边缘;(2)靠近胸壁的细胞保持有丝分裂活性;(3)有丝分裂活跃的非边缘细胞向胸壁迁移;(4)运动方向取决于PPF前后细胞之间的克隆分化。
以PPF作为有丝分裂细胞的唯一来源,PPF的早期缺陷会演变成后内侧膈肌缺陷,类似于啮齿动物硝呋烯腙CDH模型中的缺陷。如人类CDH中出现的后外侧缺陷,通过引入其他细胞贡献将更容易重现。我们的结果表明,最近关于啮齿动物中PPF主导膈肌形态发生的报道可能并不严格适用于人类。使用实验数据和可检验假设相结合的方法重现CDH缺陷的能力,推动了模拟建模作为膈肌形态发生实验分析辅助手段的发展。