Greene Arin K, Wiener Stephen, Puder Mark, Yoshida Atsushi, Shi Bin, Perez-Atayde Antonio R, Efstathiou Jason A, Holmgren Lars, Adamis Anthony P, Rupnick Maria, Folkman Judah, O'Reilly Michael S
Department of Surgery, Children's Hospital, Harvard Medical School, 300 Longwood Avenue, Hunnewell 103, Boston, MA 02115, USA.
Ann Surg. 2003 Apr;237(4):530-5. doi: 10.1097/01.SLA.0000059986.96051.EA.
To determine the role of the microvascular endothelium in the regulation of regenerating liver mass after partial hepatectomy.
Angiogenesis is critical for both pathologic and physiologic processes. The ability of certain tissues, such as the liver, kidney, and spleen, to regenerate after injury is poorly understood. The liver will regenerate to its normal mass within 8 days of surgical excision. Because the authors have previously shown that the endothelial cell regulates tumor mass, we hypothesized that normal adult organ mass is also controlled by the endothelial cell.
Two-thirds partial hepatectomy was performed in 7- to 8-week-old C57 BL/6 mice, followed by systemic treatment with either the angiogenesis stimulator basic fibroblast growth factor (bFGF) (1 microg/g/d intraperitoneal) or the angiogenesis inhibitor TNP-470 (30 mg/kg/qod subcutaneous). Groups of three mice were then euthanized on postoperative days 2, 4, 6, and 8, and the livers were weighed and analyzed by immunohistochemistry.
bFGF accelerated hepatic regeneration by 42%, 19%, 16%, and 16% on postoperative days 2, 4, 6, and 8, respectively. TNP-470 inhibited hepatic regeneration by 46%, 74%, 67%, and 64% on postoperative days 2, 4, 6, and 8, respectively. Immunohistochemistry revealed that bFGF and TNP-470 primarily affected the endothelial compartment. Specifically, bFGF increased endothelial proliferation and decreased endothelial apoptosis. TNP-470, in contrast, inhibited endothelial cell proliferation. The cessation of the regenerative process correlated with a decrease in endothelial proliferation and an increase in endothelial apoptosis.
The systemic administration of angiogenesis agents modulates the regeneration of hepatic mass primarily by affecting endothelial cell proliferation or apoptosis. Endothelial cell apoptosis is associated with the cessation of the regenerative process in control mice. These results suggest that the endothelial cell is one of the key mediators of regenerating adult tissue mass in this partial hepatectomy model.
确定微血管内皮细胞在部分肝切除术后再生肝质量调节中的作用。
血管生成对病理和生理过程都至关重要。某些组织,如肝脏、肾脏和脾脏,损伤后再生的能力尚不清楚。肝脏在手术切除后8天内会再生至正常质量。因为作者之前已表明内皮细胞调节肿瘤质量,所以我们推测正常成体器官质量也受内皮细胞控制。
对7至8周龄的C57 BL/6小鼠进行三分之二部分肝切除术,随后分别用血管生成刺激剂碱性成纤维细胞生长因子(bFGF)(1微克/克/天腹腔注射)或血管生成抑制剂TNP - 470(30毫克/千克/隔日皮下注射)进行全身治疗。然后在术后第2、4、6和8天对每组三只小鼠实施安乐死,称量肝脏重量并通过免疫组织化学进行分析。
bFGF在术后第2、4、6和8天分别使肝再生加速42%、19%、16%和16%。TNP - 470在术后第2、4、6和8天分别抑制肝再生46%、74%、67%和64%。免疫组织化学显示bFGF和TNP - 470主要影响内皮细胞区室。具体而言,bFGF增加内皮细胞增殖并减少内皮细胞凋亡。相比之下,TNP - 470抑制内皮细胞增殖。再生过程的停止与内皮细胞增殖减少和内皮细胞凋亡增加相关。
血管生成剂的全身给药主要通过影响内皮细胞增殖或凋亡来调节肝质量的再生。在对照小鼠中,内皮细胞凋亡与再生过程的停止相关。这些结果表明,在该部分肝切除模型中,内皮细胞是成体组织质量再生的关键介质之一。