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KLF2(肺 Kruppel 样因子 2)通过调节自噬来调节破骨细胞的生成。

KLF2 (kruppel-like factor 2 [lung]) regulates osteoclastogenesis by modulating autophagy.

机构信息

Department of Pharmaceutical Sciences, School of Pharmacy, Texas Tech University Health Sciences Center, Amarillo, TX, USA.

出版信息

Autophagy. 2019 Dec;15(12):2063-2075. doi: 10.1080/15548627.2019.1596491. Epub 2019 Apr 16.

Abstract

Macroautophagy/autophagy is involved in myeloid cellular repair, destruction, and osteoclast differentiation; conversely, KLF2 (kruppel-like factor 2 [lung]) regulates myeloid cell activation and differentiation. To investigate the specific role of KLF2 in autophagy, osteoclastic differentiation was induced in monocytes in presence or absence of the autophagy inhibitor 3-methyladenine (3-MA), KLF2 inducer geranylgeranyl transferase inhibitor (GGTI298), and adenoviral overexpression of KLF2. We found that the number of autophagic cells and multinucleated osteoclasts were significantly decreased in presence of 3-MA, GGTI298, and KLF2 overexpressed cells indicating involvement of KLF2 in these processes. In addition, autophagy-related protein molecules were significantly decreased after induction of KLF2 during the course of osteoclastic differentiation. Furthermore, induction of arthritis in mice reduced the level of in monocytes, and enhanced autophagy during osteoclastic differentiation. Mechanistically, knocking down of KLF2 increased the level of Beclin1 (BECN1) expression, and conversely, KLF2 over-expression reduced the level of BECN1 in monocytes. Moreover, 3-MA and GGTI298 both reduced myeloid cell proliferation concomitantly upregulating senescence-related molecules (CDKN1A/p21 and CDKN1B/p27). We further confirmed epigenetic regulation of by modulating ; knocking down of increased the levels of histone activation marks H3K9 and H4K8 acetylation in the promoter region of ; and overexpression of decreased the levels of H4K8 and H3K9 acetylation. In addition, osteoclastic differentiation also increased levels of H3K9 and H4K8 acetylation in the promoter region of . Together these findings for the first time revealed that critically regulates -mediated autophagy process during osteoclastogenesis.: ACP5/TRAP: acid phosphatase 5, tartrate resistant; Ad-KLF2: adenoviral construct of KLF2; ATG3: autophagy related 3; ATG5: autophagy related 5; ATG7: autophagy related 7; ATG12: autophagy related 12; BECN1: beclin 1, autophagy related; C57BL/6: inbred mouse strain C57 black 6; ChIP: chromatin immunoprecipitation; CSF1/MCSF: colony stimulating factor 1 (macrophage); CTSK: cathepsin K; EV: empty vector; GGTI298: geranylgeranyl transferase inhibitor; H3K9Ac: histone H3 lysine 9 acetylation; H4K8Ac: histone H4 lysine 8 acetylation; K/BxN mice: T cell receptor (TCR) transgene KRN and the MHC class II molecule A(g7) generates K/BxN mice; KLF2: kruppel-like factor 2 (lung); 3MA: 3-methyladenine; MAP1LC3B/LC3B: microtubule-associated protein 1 light chain 3 beta; MDC: monodansylcadaverine; NFATc1: nuclear factor of activated T cells 1; NFKB: nuclear factor of kappa light polypeptide gene enhancer in B cells; p21/CDKN1A: cyclin dependent kinase inhibitor 1A; p27/CDKN1B: cyclin-dependent kinase inhibitor 1B; PCR: polymerase chain reaction; PtdIns3K: phosphoinositide 3-kinase; RA: rheumatoid arthritis; si: small interfering KLF2 ribonucleic acid; NS: non-specific; RAW 264.7: abelson murine leukemia virus transformed macrophage cell line; TNFSF11/RANKL: tumor necrosis factor (ligand) superfamily, member 11; TSS: transcriptional start site; UCSC: University of California, Santa Cruz.

摘要

自噬参与骨髓细胞的修复、破坏和破骨细胞分化;相反,KLF2(肺)调节骨髓细胞的激活和分化。为了研究 KLF2 在自噬中的特异性作用,在单核细胞中诱导破骨细胞分化,同时存在或不存在自噬抑制剂 3-甲基腺嘌呤(3-MA)、KLF2 诱导剂香叶基转移酶抑制剂(GGTI298)和 KLF2 过表达腺病毒。我们发现,在存在 3-MA、GGTI298 和 KLF2 过表达细胞的情况下,自噬细胞和多核破骨细胞的数量明显减少,表明 KLF2 参与了这些过程。此外,在破骨细胞分化过程中诱导 KLF2 后,自噬相关蛋白分子的水平显著降低。此外,在关节炎诱导的小鼠中,单核细胞中的水平降低,并增强了破骨细胞分化过程中的自噬作用。从机制上讲,敲低 KLF2 增加了 Beclin1(BECN1)表达水平,相反,KLF2 过表达降低了单核细胞中的 BECN1 水平。此外,3-MA 和 GGTI298 均降低了骨髓细胞的增殖,同时上调了衰老相关分子(CDKN1A/p21 和 CDKN1B/p27)。我们进一步证实了通过调节表观遗传调控。敲低增加了启动子区域 H3K9 和 H4K8 乙酰化的组蛋白激活标记水平;而过表达则降低了 H4K8 和 H3K9 乙酰化水平。此外,破骨细胞分化也增加了启动子区域的 H3K9 和 H4K8 乙酰化水平。这些发现首次揭示了在破骨细胞发生过程中,关键地调节了由介导的自噬过程。

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