
Journal of International Obstetrics and Gynecology ›› 2025, Vol. 52 ›› Issue (4): 462-466.doi: 10.12280/gjfckx.20250022
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ZHAO Ming, ZHAN Hong, WU Rui-jin△(
)
Received:2025-01-08
Published:2025-08-15
Online:2025-09-08
Contact:
WU Rui-jin, E-mail: ZHAO Ming, ZHAN Hong, WU Rui-jin. Research Advances in Platelet Rich Plasma Therapy for Premature Ovarian Insufficiency[J]. Journal of International Obstetrics and Gynecology, 2025, 52(4): 462-466.
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| 成分 | 作用机制 | 功能 |
|---|---|---|
| PDGF[ | 通过结合并激活2个结构相关的蛋白酪氨酸激酶受体(α受体和β受体)发挥其细胞效应;诱导肌动蛋白系统的重组并促使细胞沿着PDGF浓度梯度定向迁移;通过RAS-MAPK、PI3K和磷脂酶C-γ等信号通路发挥作用 | 促进血管生成;促进有丝分裂;活化巨噬细胞 |
| TGF-β[ | 是细胞生长和分化的关键调节蛋白,其中包括生长分化因子-9、骨形成蛋白-15,在早期卵泡发生和排卵中起重要作用;通过Smad2和Smad3发出信号,并转位到细胞核,调控靶基因的表达 | 促进组织再生愈合;调节炎症;诱导细胞增殖分化 |
| VEGF[ | 可作为颗粒细胞的生存因子;通过抑制胱天蛋白酶3的激活增强滤泡细胞的存活能力;通过激活PI3K/蛋白激酶B和丝裂原活化蛋白激酶激酶/ERK通路发挥作用 | 促进血管生成;抑制卵泡闭锁 |
| EGF[ | 是一种有效的上游功能因子;是CDC42的快速激活剂;通过提高CDC42-PI3K信号活性改善原始卵泡的瞬时激活;通过ERK1/2、PI3K等通路促进细胞减数分裂;通过MAPK和PI3K通路增强卵巢基质细胞的增殖 | 促进血管生成;促进细胞生成、增殖、分化 |
| HGF[ | 窦前卵泡抗细胞凋亡的关键调节因子;阻止可能导致卵泡闭锁的卵泡内类固醇的异常积累 | 促进血管生成;抑制细胞凋亡 |
| FGF[ | 是颗粒细胞内有效的有丝分裂因子,刺激颗粒细胞的DNA合成;通过抑制Hippo通路并上调活性Yes相关蛋白表达增强颗粒细胞的抗凋亡能力 | 促进血管生成;促进细胞增殖 |
| IGF-1[ | 调节颗粒细胞发育及功能的生长因子;以自分泌的形式刺激颗粒细胞的复制及分化 | 促进血管生成;抑制细胞凋亡;维持卵泡发育 |
| 成分 | 作用机制 | 功能 |
|---|---|---|
| PDGF[ | 通过结合并激活2个结构相关的蛋白酪氨酸激酶受体(α受体和β受体)发挥其细胞效应;诱导肌动蛋白系统的重组并促使细胞沿着PDGF浓度梯度定向迁移;通过RAS-MAPK、PI3K和磷脂酶C-γ等信号通路发挥作用 | 促进血管生成;促进有丝分裂;活化巨噬细胞 |
| TGF-β[ | 是细胞生长和分化的关键调节蛋白,其中包括生长分化因子-9、骨形成蛋白-15,在早期卵泡发生和排卵中起重要作用;通过Smad2和Smad3发出信号,并转位到细胞核,调控靶基因的表达 | 促进组织再生愈合;调节炎症;诱导细胞增殖分化 |
| VEGF[ | 可作为颗粒细胞的生存因子;通过抑制胱天蛋白酶3的激活增强滤泡细胞的存活能力;通过激活PI3K/蛋白激酶B和丝裂原活化蛋白激酶激酶/ERK通路发挥作用 | 促进血管生成;抑制卵泡闭锁 |
| EGF[ | 是一种有效的上游功能因子;是CDC42的快速激活剂;通过提高CDC42-PI3K信号活性改善原始卵泡的瞬时激活;通过ERK1/2、PI3K等通路促进细胞减数分裂;通过MAPK和PI3K通路增强卵巢基质细胞的增殖 | 促进血管生成;促进细胞生成、增殖、分化 |
| HGF[ | 窦前卵泡抗细胞凋亡的关键调节因子;阻止可能导致卵泡闭锁的卵泡内类固醇的异常积累 | 促进血管生成;抑制细胞凋亡 |
| FGF[ | 是颗粒细胞内有效的有丝分裂因子,刺激颗粒细胞的DNA合成;通过抑制Hippo通路并上调活性Yes相关蛋白表达增强颗粒细胞的抗凋亡能力 | 促进血管生成;促进细胞增殖 |
| IGF-1[ | 调节颗粒细胞发育及功能的生长因子;以自分泌的形式刺激颗粒细胞的复制及分化 | 促进血管生成;抑制细胞凋亡;维持卵泡发育 |
| 文献 | 组织 类型 | 动物 模型 | 干预措施 | 样本量 (只) | 研究结果 |
|---|---|---|---|---|---|
| Shivaramu等[ | 肝脏 | 大鼠 | 将大鼠随机分为空白对照组、干细胞组(5×106)、0.5 mL PRP组、0.35 mg/kg HGF组、干细胞+PRP组、干细胞+HGF组、PRP+HGF组、干细胞+PRP+HGF组,每组20只 | 160 | 联合治疗比单独使用PRP或HGF显示出更好的护肝作用;干细胞、PRP和HGF对胆汁淤积诱导的肝纤维化具有协同改善及再生的作用 |
| Marchante等[ | 卵巢 | 小鼠 | 将8周龄年轻小鼠、28周龄中年小鼠和36周龄老年小鼠分别随机分为10 μL生理盐水空白组、10 μL PRP组和10 μL干细胞+PRP组,每组4只 | 36 | PRP治疗激活卵泡的效率低于干细胞联合PRP治疗 |
| Zhang等[ | 骨关节 | 兔 | 将兔随机分为假手术组、0.3 mL生理盐水空白组、0.3 mL PRP组、0.3 mL干细胞组(1×106/mL)、0.3 mL干细胞+PRP组,每组10只 | 50 | PRP可增强干细胞的生物活性,包括增殖、迁移和黏附;联合治疗增强了软骨细胞的活性氧清除能力并抑制了细胞凋亡 |
| Akbari等[ | 神经 | 大鼠 | 将大鼠随机分为健康对照组、假手术组、PBS组、500 μL PRP组、干细胞组(1×106)、干细胞+PRP组 | 58 | 联合治疗组在空间记忆改善方面表现更好;仅有联合治疗组恢复了基底突触传递 |
| 文献 | 组织 类型 | 动物 模型 | 干预措施 | 样本量 (只) | 研究结果 |
|---|---|---|---|---|---|
| Shivaramu等[ | 肝脏 | 大鼠 | 将大鼠随机分为空白对照组、干细胞组(5×106)、0.5 mL PRP组、0.35 mg/kg HGF组、干细胞+PRP组、干细胞+HGF组、PRP+HGF组、干细胞+PRP+HGF组,每组20只 | 160 | 联合治疗比单独使用PRP或HGF显示出更好的护肝作用;干细胞、PRP和HGF对胆汁淤积诱导的肝纤维化具有协同改善及再生的作用 |
| Marchante等[ | 卵巢 | 小鼠 | 将8周龄年轻小鼠、28周龄中年小鼠和36周龄老年小鼠分别随机分为10 μL生理盐水空白组、10 μL PRP组和10 μL干细胞+PRP组,每组4只 | 36 | PRP治疗激活卵泡的效率低于干细胞联合PRP治疗 |
| Zhang等[ | 骨关节 | 兔 | 将兔随机分为假手术组、0.3 mL生理盐水空白组、0.3 mL PRP组、0.3 mL干细胞组(1×106/mL)、0.3 mL干细胞+PRP组,每组10只 | 50 | PRP可增强干细胞的生物活性,包括增殖、迁移和黏附;联合治疗增强了软骨细胞的活性氧清除能力并抑制了细胞凋亡 |
| Akbari等[ | 神经 | 大鼠 | 将大鼠随机分为健康对照组、假手术组、PBS组、500 μL PRP组、干细胞组(1×106)、干细胞+PRP组 | 58 | 联合治疗组在空间记忆改善方面表现更好;仅有联合治疗组恢复了基底突触传递 |
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