Dobrzynski H, Li J, Tellez J, Greener I D, Nikolski V P, Wright S E, Parson S H, Jones S A, Lancaster M K, Yamamoto M, Honjo H, Takagishi Y, Kodama I, Efimov I R, Billeter R, Boyett M R
University of Leeds, Leeds LS2 9JT, UK.
Circulation. 2005 Feb 22;111(7):846-54. doi: 10.1161/01.CIR.0000152100.04087.DB. Epub 2005 Feb 7.
There is an effort to build an anatomically and biophysically detailed virtual heart, and, although there are models for the atria and ventricles, there is no model for the sinoatrial node (SAN). For the SAN to show pacemaking and drive atrial muscle, theoretically, there should be a gradient in electrical coupling from the center to the periphery of the SAN and an interdigitation of SAN and atrial cells at the periphery. Any model should include such features.
Staining of rabbit SAN preparations for histology, middle neurofilament, atrial natriuretic peptide, and connexin (Cx) 43 revealed multiple cell types within and around the SAN (SAN and atrial cells, fibroblasts, and adipocytes). In contrast to atrial cells, all SAN cells expressed middle neurofilament (but not atrial natriuretic peptide) mRNA and protein. However, 2 distinct SAN cell types were observed: cells in the center (leading pacemaker site) were small, were organized in a mesh, and did not express Cx43. In contrast, cells in the periphery (exit pathway from the SAN) were large, were arranged predominantly in parallel, often expressed Cx43, and were mixed with atrial cells. An approximately 2.5-million-element array model of the SAN and surrounding atrium, incorporating all cell types, was constructed.
For the first time, a 3D anatomically detailed mathematical model of the SAN has been constructed, and this shows the presence of a specialized interface between the SAN and atrial muscle.
目前正在努力构建一个在解剖学和生物物理学方面细节丰富的虚拟心脏,尽管已经有了心房和心室的模型,但尚无窦房结(SAN)的模型。从理论上讲,要使窦房结发挥起搏作用并驱动心房肌,窦房结从中心到周边应存在电耦合梯度,且在周边窦房结细胞与心房细胞应相互交错。任何模型都应具备这些特征。
对兔窦房结标本进行组织学、中间丝、心房利钠肽和连接蛋白(Cx)43染色,结果显示窦房结内部及周围存在多种细胞类型(窦房结细胞和心房细胞、成纤维细胞和脂肪细胞)。与心房细胞不同,所有窦房结细胞均表达中间丝(而非心房利钠肽)的mRNA和蛋白。然而,观察到两种不同的窦房结细胞类型:中心部位的细胞(主要起搏位点)较小,呈网状排列,不表达Cx43。相比之下,周边部位的细胞(窦房结的传出通路)较大,主要呈平行排列,常表达Cx43,并与心房细胞混合。构建了一个包含所有细胞类型的约250万个单元的窦房结及周围心房的阵列模型。
首次构建了一个三维解剖学细节丰富的窦房结数学模型,该模型显示窦房结与心房肌之间存在一个特殊界面。